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 ACC 10 122643301 122643301 + Missense_Mutation SNP G G T TCGA-OR-A5J6-01A-31D-A29I-10 TCGA-OR-A5J6-10A-01D-A29L-10 g.chr10:122643301G>T c.1749G>T c.(1747-1749)ttG>ttT p.L583F BLCA 10 122612070 122612070 + Missense_Mutation SNP T T C TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr10:122612070T>C c.121T>C c.(121-123)Tca>Cca p.S41P BLCA 10 122618238 122618238 + Missense_Mutation SNP G G T TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr10:122618238G>T c.282G>T c.(280-282)aaG>aaT p.K94N BLCA 10 122619733 122619733 + Missense_Mutation SNP G G C TCGA-DK-A1AA-01A-11D-A13W-08 TCGA-DK-A1AA-10A-01D-A13W-08 g.chr10:122619733G>C c.465G>C c.(463-465)aaG>aaC p.K155N BLCA 10 122622380 122622380 + Silent SNP T T A TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chr10:122622380T>A c.660T>A c.(658-660)ggT>ggA p.G220G BLCA 10 122622425 122622425 + Silent SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr10:122622425G>A c.705G>A c.(703-705)gaG>gaA p.E235E BLCA 10 122624668 122624668 + Missense_Mutation SNP G G C TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr10:122624668G>C c.823G>C c.(823-825)Gtg>Ctg p.V275L BLCA 10 122626229 122626229 + Missense_Mutation SNP G G A TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chr10:122626229G>A c.1143G>A c.(1141-1143)atG>atA p.M381I BLCA 10 122626260 122626260 + Silent SNP C C A TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr10:122626260C>A c.1174C>A c.(1174-1176)Cga>Aga p.R392R BLCA 10 122630833 122630833 + Missense_Mutation SNP G G C TCGA-GU-AATO-01A-11D-A391-08 TCGA-GU-AATO-10A-01D-A394-08 g.chr10:122630833G>C c.1446G>C c.(1444-1446)aaG>aaC p.K482N BLCA 10 122633428 122633428 + Missense_Mutation SNP G G A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr10:122633428G>A c.1549G>A c.(1549-1551)Gaa>Aaa p.E517K BLCA 10 122637962 122637962 + Missense_Mutation SNP C C T TCGA-FD-A3SN-01A-12D-A22Z-08 TCGA-FD-A3SN-10A-01D-A22Z-08 g.chr10:122637962C>T c.1654C>T c.(1654-1656)Ctt>Ttt p.L552F BLCA 10 122648591 122648591 + Splice_Site SNP G G A TCGA-GC-A3I6-01A-11D-A20D-08 TCGA-GC-A3I6-10A-01D-A20D-08 g.chr10:122648591G>A c.2123G>A c.(2122-2124)gGa>gAa p.G708E BLCA 10 122659635 122659635 + Missense_Mutation SNP G G C TCGA-DK-AA74-01A-11D-A391-08 TCGA-DK-AA74-10A-01D-A394-08 g.chr10:122659635G>C c.2610G>C c.(2608-2610)ttG>ttC p.L870F BLCA 10 122660558 122660558 + Missense_Mutation SNP G G A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr10:122660558G>A c.2635G>A c.(2635-2637)Gaa>Aaa p.E879K BLCA 10 122661814 122661814 + Silent SNP G G A TCGA-GU-AATO-01A-11D-A391-08 TCGA-GU-AATO-10A-01D-A394-08 g.chr10:122661814G>A c.2733G>A c.(2731-2733)caG>caA p.Q911Q BLCA 10 122664181 122664181 + Silent SNP G G T TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr10:122664181G>T c.3051G>T c.(3049-3051)ctG>ctT p.L1017L BRCA 10 122618231 122618231 + Missense_Mutation SNP A A G TCGA-E9-A22D-01A-11D-A159-09 TCGA-E9-A22D-10A-01D-A159-09 g.chr10:122618231A>G c.275A>G c.(274-276)aAt>aGt p.N92S BRCA 10 122622406 122622406 + Missense_Mutation SNP A A G TCGA-E2-A1IN-01A-11D-A13L-09 TCGA-E2-A1IN-10A-01D-A188-09 g.chr10:122622406A>G c.686A>G c.(685-687)aAa>aGa p.K229R BRCA 10 122643389 122643389 + Missense_Mutation SNP A A G TCGA-EW-A1IZ-01A-11D-A188-09 TCGA-EW-A1IZ-10A-01D-A13O-09 g.chr10:122643389A>G c.1837A>G c.(1837-1839)Ata>Gta p.I613V BRCA 10 122646224 122646234 + Frame_Shift_Del DEL AATCTGAACTT AATCTGAACTT - TCGA-A2-A0T0-01A-22D-A099-09 TCGA-A2-A0T0-10A-01D-A099-09 g.chr10:122646224_122646234delAATCTGAACTT c.1997_2007delAATCTGAACTT c.(1996-2007)aaatctgaacttfs p.KSEL666fs BRCA 10 122648628 122648628 + Silent SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:122648628T>G c.2160T>G c.(2158-2160)ggT>ggG p.G720G BRCA 10 122649430 122649430 + Missense_Mutation SNP G G C TCGA-A8-A092-01A-11W-A019-09 TCGA-A8-A092-10A-01W-A021-09 g.chr10:122649430G>C c.2252G>C c.(2251-2253)tGg>tCg p.W751S CESC 10 122633397 122633397 + Silent SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr10:122633397G>C c.1518G>C c.(1516-1518)ctG>ctC p.L506L CESC 10 122664255 122664255 + Missense_Mutation SNP C C T TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr10:122664255C>T c.3125C>T c.(3124-3126)tCg>tTg p.S1042L CHOL 10 122661797 122661797 + Nonsense_Mutation SNP G G T TCGA-W5-AA30-01A-31D-A417-09 TCGA-W5-AA30-10A-01D-A41A-09 g.chr10:122661797G>T c.2716G>T c.(2716-2718)Gaa>Taa p.E906* COAD 10 122619679 122619679 + Silent SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr10:122619679G>A c.411G>A c.(409-411)ccG>ccA p.P137P COAD 10 122624604 122624604 + Silent SNP G G T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr10:122624604G>T c.759G>T c.(757-759)ctG>ctT p.L253L COAD 10 122625220 122625220 + Missense_Mutation SNP T T C TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr10:122625220T>C c.958T>C c.(958-960)Tat>Cat p.Y320H COAD 10 122640355 122640355 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr10:122640355C>T c.1681C>T c.(1681-1683)Cgt>Tgt p.R561C COAD 10 122643322 122643322 + Silent SNP A A G TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr10:122643322A>G c.1770A>G c.(1768-1770)aaA>aaG p.K590K COAD 10 122643379 122643379 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:122643379C>T c.1827C>T c.(1825-1827)aaC>aaT p.N609N COAD 10 122649410 122649410 + Silent SNP A A G TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:122649410A>G c.2232A>G c.(2230-2232)ggA>ggG p.G744G COAD 10 122649444 122649444 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:122649444C>T c.2266C>T c.(2266-2268)Cgt>Tgt p.R756C COAD 10 122650306 122650306 + Missense_Mutation SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr10:122650306A>G c.2422A>G c.(2422-2424)Aaa>Gaa p.K808E COAD 10 122650314 122650314 + Silent SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:122650314C>A c.2430C>A c.(2428-2430)atC>atA p.I810I COAD 10 122661812 122661812 + Nonsense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr10:122661812C>T c.2731C>T c.(2731-2733)Cag>Tag p.Q911* COAD 10 122662711 122662711 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr10:122662711C>T c.2898C>T c.(2896-2898)tgC>tgT p.C966C COAD 10 122662745 122662745 + Splice_Site SNP G G T TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr10:122662745G>T c.e23+1 COAD 10 122664840 122664840 + Missense_Mutation SNP A A G TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr10:122664840A>G c.3203A>G c.(3202-3204)cAg>cGg p.Q1068R COAD 10 122664871 122664871 + Silent SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr10:122664871C>T c.3234C>T c.(3232-3234)gaC>gaT p.D1078D COAD 10 122665414 122665414 + Silent SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr10:122665414C>T c.3318C>T c.(3316-3318)gcC>gcT p.A1106A COAD 10 122665427 122665427 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr10:122665427C>T c.3331C>T c.(3331-3333)Cgg>Tgg p.R1111W COAD 10 122665441 122665441 + Silent SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr10:122665441C>T c.3345C>T c.(3343-3345)caC>caT p.H1115H COAD 10 122668142 122668142 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:122668142C>A c.3592C>A c.(3592-3594)Ctc>Atc p.L1198I COADREAD 10 122619679 122619679 + Silent SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr10:122619679G>A c.411G>A c.(409-411)ccG>ccA p.P137P COADREAD 10 122624604 122624604 + Silent SNP G G T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr10:122624604G>T c.759G>T c.(757-759)ctG>ctT p.L253L COADREAD 10 122625220 122625220 + Missense_Mutation SNP T T C TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr10:122625220T>C c.958T>C c.(958-960)Tat>Cat p.Y320H COADREAD 10 122633433 122633433 + Silent SNP C C A TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr10:122633433C>A c.1554C>A c.(1552-1554)gtC>gtA p.V518V COADREAD 10 122640355 122640355 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr10:122640355C>T c.1681C>T c.(1681-1683)Cgt>Tgt p.R561C COADREAD 10 122643322 122643322 + Silent SNP A A G TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr10:122643322A>G c.1770A>G c.(1768-1770)aaA>aaG p.K590K COADREAD 10 122643379 122643379 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:122643379C>T c.1827C>T c.(1825-1827)aaC>aaT p.N609N COADREAD 10 122648616 122648616 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:122648616C>T c.2148C>T c.(2146-2148)atC>atT p.I716I COADREAD 10 122649410 122649410 + Silent SNP A A G TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:122649410A>G c.2232A>G c.(2230-2232)ggA>ggG p.G744G COADREAD 10 122649444 122649444 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:122649444C>T c.2266C>T c.(2266-2268)Cgt>Tgt p.R756C COADREAD 10 122649475 122649475 + Nonsense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr10:122649475T>G c.2297T>G c.(2296-2298)tTa>tGa p.L766* COADREAD 10 122650306 122650306 + Missense_Mutation SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr10:122650306A>G c.2422A>G c.(2422-2424)Aaa>Gaa p.K808E COADREAD 10 122650314 122650314 + Silent SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:122650314C>A c.2430C>A c.(2428-2430)atC>atA p.I810I COADREAD 10 122661812 122661812 + Nonsense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr10:122661812C>T c.2731C>T c.(2731-2733)Cag>Tag p.Q911* COADREAD 10 122662711 122662711 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr10:122662711C>T c.2898C>T c.(2896-2898)tgC>tgT p.C966C COADREAD 10 122662745 122662745 + Splice_Site SNP G G T TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr10:122662745G>T c.e23+1 COADREAD 10 122664840 122664840 + Missense_Mutation SNP A A G TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr10:122664840A>G c.3203A>G c.(3202-3204)cAg>cGg p.Q1068R COADREAD 10 122664871 122664871 + Silent SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr10:122664871C>T c.3234C>T c.(3232-3234)gaC>gaT p.D1078D COADREAD 10 122665414 122665414 + Silent SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr10:122665414C>T c.3318C>T c.(3316-3318)gcC>gcT p.A1106A COADREAD 10 122665427 122665427 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr10:122665427C>T c.3331C>T c.(3331-3333)Cgg>Tgg p.R1111W COADREAD 10 122665441 122665441 + Silent SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr10:122665441C>T c.3345C>T c.(3343-3345)caC>caT p.H1115H COADREAD 10 122668142 122668142 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:122668142C>A c.3592C>A c.(3592-3594)Ctc>Atc p.L1198I COADREAD 10 122668211 122668211 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:122668211C>T c.3661C>T c.(3661-3663)Ccc>Tcc p.P1221S DLBC 10 122610983 122610983 + Silent SNP G G T TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr10:122610983G>T c.51G>T c.(49-51)ggG>ggT p.G17G DLBC 10 122649481 122649481 + Missense_Mutation SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr10:122649481C>T c.2303C>T c.(2302-2304)gCa>gTa p.A768V DLBC 10 122668181 122668181 + Silent SNP T T C TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr10:122668181T>C c.3631T>C c.(3631-3633)Ttg>Ctg p.L1211L ESCA 10 122630715 122630715 + Missense_Mutation SNP G G T TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr10:122630715G>T c.1328G>T c.(1327-1329)aGa>aTa p.R443I ESCA 10 122660587 122660587 + Missense_Mutation SNP A A T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr10:122660587A>T c.2664A>T c.(2662-2664)caA>caT p.Q888H ESCA 10 122663626 122663626 + Missense_Mutation SNP G G T TCGA-L5-A4OU-01A-11D-A28B-09 TCGA-L5-A4OU-11A-11D-A28E-09 g.chr10:122663626G>T c.2999G>T c.(2998-3000)tGt>tTt p.C1000F GBM 10 122622305 122622305 + Silent SNP A A G TCGA-28-5211-01C-11D-1845-08 TCGA-28-5211-10B-01D-1845-08 g.chr10:122622305A>G c.585A>G c.(583-585)tcA>tcG p.S195S GBM 10 122645345 122645345 + Missense_Mutation SNP A A G TCGA-16-1045-01B-01W-0611-08 TCGA-16-1045-10B-01W-0611-08 g.chr10:122645345A>G c.1868A>G c.(1867-1869)aAc>aGc p.N623S GBM 10 122649467 122649467 + Silent SNP T T C TCGA-76-6662-01A-11D-1845-08 TCGA-76-6662-10A-01D-1845-08 g.chr10:122649467T>C c.2289T>C c.(2287-2289)aaT>aaC p.N763N GBMLGG 10 122619736 122619736 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:122619736C>A c.468C>A c.(466-468)agC>agA p.S156R GBMLGG 10 122622305 122622305 + Silent SNP A A G TCGA-28-5211-01C-11D-1845-08 TCGA-28-5211-10B-01D-1845-08 g.chr10:122622305A>G c.585A>G c.(583-585)tcA>tcG p.S195S GBMLGG 10 122645345 122645345 + Missense_Mutation SNP A A G TCGA-16-1045-01B-01W-0611-08 TCGA-16-1045-10B-01W-0611-08 g.chr10:122645345A>G c.1868A>G c.(1867-1869)aAc>aGc p.N623S GBMLGG 10 122649467 122649467 + Silent SNP T T C TCGA-76-6662-01A-11D-1845-08 TCGA-76-6662-10A-01D-1845-08 g.chr10:122649467T>C c.2289T>C c.(2287-2289)aaT>aaC p.N763N GBMLGG 10 122664218 122664218 + Missense_Mutation SNP G G C TCGA-FG-5965-01B-11D-1893-08 TCGA-FG-5965-10A-01D-1893-08 g.chr10:122664218G>C c.3088G>C c.(3088-3090)Gat>Cat p.D1030H GBMLGG 10 122664854 122664854 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:122664854A>G c.3217A>G c.(3217-3219)Ata>Gta p.I1073V HNSC 10 122612036 122612036 + Splice_Site SNP G G A TCGA-CV-5435-01A-01D-1683-08 TCGA-CV-5435-10A-01D-1870-08 g.chr10:122612036G>A c.87G>A c.(85-87)tgG>tgA p.W29* HNSC 10 122618278 122618278 + Missense_Mutation SNP G G A TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr10:122618278G>A c.322G>A c.(322-324)Gag>Aag p.E108K HNSC 10 122619653 122619653 + Missense_Mutation SNP C C T TCGA-CQ-5331-01A-02D-1870-08 TCGA-CQ-5331-10A-01D-1870-08 g.chr10:122619653C>T c.385C>T c.(385-387)Cgc>Tgc p.R129C HNSC 10 122622272 122622272 + Silent SNP C C T TCGA-CV-6436-01A-11D-1683-08 TCGA-CV-6436-11A-01D-1683-08 g.chr10:122622272C>T c.552C>T c.(550-552)ttC>ttT p.F184F HNSC 10 122624702 122624702 + Missense_Mutation SNP G G T TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr10:122624702G>T c.857G>T c.(856-858)cGc>cTc p.R286L HNSC 10 122630711 122630711 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr10:122630711C>T c.1324C>T c.(1324-1326)Ccc>Tcc p.P442S HNSC 10 122633434 122633437 + Splice_Site DEL AAGT AAGT - TCGA-DQ-7593-01A-11D-2229-08 TCGA-DQ-7593-10D-01D-2229-08 g.chr10:122633434_122633437delAAGT c.1555_1556delAAGT c.(1555-1557)aag>g p.K519fs HNSC 10 122660595 122660595 + Missense_Mutation SNP T T G TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr10:122660595T>G c.2672T>G c.(2671-2673)tTg>tGg p.L891W HNSC 10 122660596 122660596 + Missense_Mutation SNP G G T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr10:122660596G>T c.2673G>T c.(2671-2673)ttG>ttT p.L891F HNSC 10 122662636 122662636 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr10:122662636G>A c.2823G>A c.(2821-2823)caG>caA p.Q941Q HNSC 10 122662637 122662637 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr10:122662637G>A c.2824G>A c.(2824-2826)Gaa>Aaa p.E942K HNSC 10 122664230 122664230 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr10:122664230G>A c.3100G>A c.(3100-3102)Gcc>Acc p.A1034T HNSC 10 122668114 122668114 + Silent SNP G G A TCGA-CR-6478-01A-11D-1870-08 TCGA-CR-6478-10A-01D-1870-08 g.chr10:122668114G>A c.3564G>A c.(3562-3564)aaG>aaA p.K1188K KIPAN 10 122624668 122624668 + Missense_Mutation SNP G G C TCGA-CJ-5679-01A-11D-1534-10 TCGA-CJ-5679-11A-01D-1535-10 g.chr10:122624668G>C c.823G>C c.(823-825)Gtg>Ctg p.V275L KIPAN 10 122650370 122650370 + Missense_Mutation SNP G G T TCGA-5P-A9JV-01A-12D-A42J-10 TCGA-5P-A9JV-10A-01D-A42M-10 g.chr10:122650370G>T c.2486G>T c.(2485-2487)tGc>tTc p.C829F KIPAN 10 122661797 122661797 + Nonsense_Mutation SNP G G T TCGA-CJ-4882-01A-02D-1429-08 TCGA-CJ-4882-11A-01D-1429-08 g.chr10:122661797G>T c.2716G>T c.(2716-2718)Gaa>Taa p.E906* KIPAN 10 122663626 122663626 + Missense_Mutation SNP G G A TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr10:122663626G>A c.2999G>A c.(2998-3000)tGt>tAt p.C1000Y KIPAN 10 122664157 122664157 + Splice_Site SNP G G A TCGA-HE-A5NF-01A-11D-A26P-10 TCGA-HE-A5NF-10A-01D-A26P-10 g.chr10:122664157G>A c.e25-1 KIPAN 10 122665493 122665493 + Missense_Mutation SNP T T A TCGA-AT-A5NU-01A-11D-A28G-10 TCGA-AT-A5NU-10A-01D-A28G-10 g.chr10:122665493T>A c.3397T>A c.(3397-3399)Tct>Act p.S1133T KIRC 10 122624668 122624668 + Missense_Mutation SNP G G C TCGA-CJ-5679-01A-11D-1534-10 TCGA-CJ-5679-11A-01D-1535-10 g.chr10:122624668G>C c.823G>C c.(823-825)Gtg>Ctg p.V275L KIRC 10 122661797 122661797 + Nonsense_Mutation SNP G G T TCGA-CJ-4882-01A-02D-1429-08 TCGA-CJ-4882-11A-01D-1429-08 g.chr10:122661797G>T c.2716G>T c.(2716-2718)Gaa>Taa p.E906* KIRC 10 122663626 122663626 + Missense_Mutation SNP G G A TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr10:122663626G>A c.2999G>A c.(2998-3000)tGt>tAt p.C1000Y KIRP 10 122650370 122650370 + Missense_Mutation SNP G G T TCGA-5P-A9JV-01A-12D-A42J-10 TCGA-5P-A9JV-10A-01D-A42M-10 g.chr10:122650370G>T c.2486G>T c.(2485-2487)tGc>tTc p.C829F KIRP 10 122664157 122664157 + Splice_Site SNP G G A TCGA-HE-A5NF-01A-11D-A26P-10 TCGA-HE-A5NF-10A-01D-A26P-10 g.chr10:122664157G>A c.e25-1 KIRP 10 122665493 122665493 + Missense_Mutation SNP T T A TCGA-AT-A5NU-01A-11D-A28G-10 TCGA-AT-A5NU-10A-01D-A28G-10 g.chr10:122665493T>A c.3397T>A c.(3397-3399)Tct>Act p.S1133T LGG 10 122619736 122619736 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:122619736C>A c.468C>A c.(466-468)agC>agA p.S156R LGG 10 122664218 122664218 + Missense_Mutation SNP G G C TCGA-FG-5965-01B-11D-1893-08 TCGA-FG-5965-10A-01D-1893-08 g.chr10:122664218G>C c.3088G>C c.(3088-3090)Gat>Cat p.D1030H LGG 10 122664854 122664854 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:122664854A>G c.3217A>G c.(3217-3219)Ata>Gta p.I1073V LIHC 10 122625230 122625230 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr10:122625230delT c.968delT c.(967-969)attfs p.I323fs LIHC 10 122626230 122626230 + Missense_Mutation SNP A A G TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr10:122626230A>G c.1144A>G c.(1144-1146)Ata>Gta p.I382V LIHC 10 122643322 122643322 + Silent SNP A A G TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr10:122643322A>G c.1770A>G c.(1768-1770)aaA>aaG p.K590K LIHC 10 122650234 122650234 + Missense_Mutation SNP A A C TCGA-DD-AACL-01A-11D-A40R-10 TCGA-DD-AACL-10A-01D-A40U-10 g.chr10:122650234A>C c.2350A>C c.(2350-2352)Atg>Ctg p.M784L LUAD 10 122622260 122622260 + Missense_Mutation SNP G G T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr10:122622260G>T c.540G>T c.(538-540)gaG>gaT p.E180D LUAD 10 122622304 122622304 + Missense_Mutation SNP C C T TCGA-50-5939-01A-11D-1625-08 TCGA-50-5939-11A-01D-1625-08 g.chr10:122622304C>T c.584C>T c.(583-585)tCa>tTa p.S195L LUAD 10 122630692 122630692 + Silent SNP A A T TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr10:122630692A>T c.1305A>T c.(1303-1305)gcA>gcT p.A435A LUAD 10 122630730 122630730 + Missense_Mutation SNP G G A TCGA-55-A48X-01A-11D-A24D-08 TCGA-55-A48X-10A-01D-A24F-08 g.chr10:122630730G>A c.1343G>A c.(1342-1344)cGg>cAg p.R448Q LUAD 10 122643308 122643308 + Missense_Mutation SNP G G T TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr10:122643308G>T c.1756G>T c.(1756-1758)Gta>Tta p.V586L LUAD 10 122648616 122648616 + Silent SNP C C T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr10:122648616C>T c.2148C>T c.(2146-2148)atC>atT p.I716I LUAD 10 122648679 122648679 + Silent SNP G G A TCGA-95-8494-01A-11D-2323-08 TCGA-95-8494-10A-01D-2323-08 g.chr10:122648679G>A c.2211G>A c.(2209-2211)ttG>ttA p.L737L LUAD 10 122665427 122665427 + Missense_Mutation SNP C C T TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chr10:122665427C>T c.3331C>T c.(3331-3333)Cgg>Tgg p.R1111W LUAD 10 122668120 122668120 + Silent SNP C C T TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr10:122668120C>T c.3570C>T c.(3568-3570)ctC>ctT p.L1190L LUSC 10 122618251 122618251 + Missense_Mutation SNP G G C TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr10:122618251G>C c.295G>C c.(295-297)Gat>Cat p.D99H LUSC 10 122659586 122659586 + Missense_Mutation SNP C C A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr10:122659586C>A c.2561C>A c.(2560-2562)gCc>gAc p.A854D LUSC 10 122664830 122664830 + Splice_Site SNP G G A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr10:122664830G>A c.e26-1 LUSC 10 122666322 122666322 + Missense_Mutation SNP G G A TCGA-43-3920-01A-01D-0983-08 TCGA-43-3920-10A-01D-0983-08 g.chr10:122666322G>A c.3472G>A c.(3472-3474)Gaa>Aaa p.E1158K LUSC 10 122666349 122666349 + Nonsense_Mutation SNP G G T TCGA-43-3920-01A-01D-0983-08 TCGA-43-3920-10A-01D-0983-08 g.chr10:122666349G>T c.3499G>T c.(3499-3501)Gaa>Taa p.E1167* OV 10 122663571 122663571 + Missense_Mutation SNP G G C TCGA-09-1674-01A-01W-0633-09 TCGA-09-1674-10A-01W-0633-09 g.chr10:122663571G>C c.2944G>C c.(2944-2946)Gaa>Caa p.E982Q OV 10 122664840 122664840 + Missense_Mutation SNP A A G TCGA-23-2645-01A-01W-1091-09 TCGA-23-2645-10A-01W-1091-09 g.chr10:122664840A>G c.3203A>G c.(3202-3204)cAg>cGg p.Q1068R PAAD 10 122619695 122619695 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:122619695C>A c.427C>A c.(427-429)Ctc>Atc p.L143I PAAD 10 122626665 122626665 + Silent SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:122626665C>A c.1278C>A c.(1276-1278)tcC>tcA p.S426S PAAD 10 122630757 122630757 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:122630757C>T c.1370C>T c.(1369-1371)aCg>aTg p.T457M PAAD 10 122650367 122650367 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:122650367C>T c.2483C>T c.(2482-2484)gCg>gTg p.A828V PCPG 10 122619631 122619631 + Missense_Mutation SNP G G C TCGA-RW-A681-01A-11D-A35D-08 TCGA-RW-A681-10A-01D-A35B-08 g.chr10:122619631G>C c.363G>C c.(361-363)tgG>tgC p.W121C PCPG 10 122662677 122662677 + Missense_Mutation SNP C C G TCGA-QT-A7U0-01A-11D-A35D-08 TCGA-QT-A7U0-10A-01D-A35B-08 g.chr10:122662677C>G c.2864C>G c.(2863-2865)cCt>cGt p.P955R PRAD 10 122646216 122646219 + Frame_Shift_Del DEL AGAA AGAA - TCGA-G9-6498-01A-12D-A30X-08 TCGA-G9-6498-10A-01D-A30X-08 g.chr10:122646216_122646219delAGAA c.1989_1992delAGAA c.(1987-1992)gcagaafs p.AE663fs PRAD 10 122662580 122662580 + Nonsense_Mutation SNP G G T TCGA-KK-A6E4-01A-11D-A30E-08 TCGA-KK-A6E4-11A-11D-A30H-08 g.chr10:122662580G>T c.2767G>T c.(2767-2769)Gaa>Taa p.E923* READ 10 122633433 122633433 + Silent SNP C C A TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr10:122633433C>A c.1554C>A c.(1552-1554)gtC>gtA p.V518V READ 10 122648616 122648616 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:122648616C>T c.2148C>T c.(2146-2148)atC>atT p.I716I READ 10 122649475 122649475 + Nonsense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr10:122649475T>G c.2297T>G c.(2296-2298)tTa>tGa p.L766* READ 10 122668211 122668211 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:122668211C>T c.3661C>T c.(3661-3663)Ccc>Tcc p.P1221S SARC 10 122659643 122659643 + Missense_Mutation SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr10:122659643C>T c.2618C>T c.(2617-2619)tCt>tTt p.S873F SKCM 10 122612140 122612140 + Missense_Mutation SNP T T C TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr10:122612140T>C c.191T>C c.(190-192)gTt>gCt p.V64A SKCM 10 122618232 122618232 + Silent SNP T T C TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr10:122618232T>C c.276T>C c.(274-276)aaT>aaC p.N92N SKCM 10 122622429 122622429 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr10:122622429C>T c.709C>T c.(709-711)Cct>Tct p.P237S SKCM 10 122624714 122624714 + Missense_Mutation SNP C C T TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr10:122624714C>T c.869C>T c.(868-870)cCa>cTa p.P290L SKCM 10 122625192 122625192 + Silent SNP T T C TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr10:122625192T>C c.930T>C c.(928-930)ggT>ggC p.G310G SKCM 10 122626202 122626202 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:122626202C>T c.1116C>T c.(1114-1116)gcC>gcT p.A372A SKCM 10 122630798 122630798 + Missense_Mutation SNP C C T TCGA-EE-A29N-06A-12D-A197-08 TCGA-EE-A29N-10A-01D-A199-08 g.chr10:122630798C>T c.1411C>T c.(1411-1413)Cgt>Tgt p.R471C SKCM 10 122648694 122648694 + Silent SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr10:122648694C>T c.2226C>T c.(2224-2226)tcC>tcT p.S742S SKCM 10 122664262 122664262 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:122664262C>T c.3132C>T c.(3130-3132)ggC>ggT p.G1044G SKCM 10 122664263 122664263 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:122664263C>T c.3133C>T c.(3133-3135)Ccc>Tcc p.P1045S SKCM 10 122664264 122664264 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:122664264C>T c.3134C>T c.(3133-3135)cCc>cTc p.P1045L SKCM 10 122665387 122665387 + Splice_Site SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr10:122665387G>A c.e27-1 SKCM 10 122665388 122665388 + Splice_Site SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr10:122665388G>A c.3292G>A c.(3292-3294)Gtc>Atc p.V1098I SKCM 10 122665478 122665478 + Missense_Mutation SNP C C T TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr10:122665478C>T c.3382C>T c.(3382-3384)Ctc>Ttc p.L1128F SKCM 10 122665480 122665480 + Silent SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr10:122665480C>T c.3384C>T c.(3382-3384)ctC>ctT p.L1128L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 10 122619733 122619733 single base substitution G C 5_prime_UTR_variant BLCA-US 10 122619733 122619733 single base substitution G C downstream_gene_variant BLCA-US 10 122619733 122619733 single base substitution G C exon_variant BLCA-US 10 122619733 122619733 single base substitution G C intron_variant BLCA-US 10 122619733 122619733 single base substitution G C missense_variant K155N 465G>C BLCA-US 10 122619733 122619733 single base substitution G C upstream_gene_variant BLCA-US 10 122622425 122622425 single base substitution G A 5_prime_UTR_variant BLCA-US 10 122622425 122622425 single base substitution G A downstream_gene_variant BLCA-US 10 122622425 122622425 single base substitution G A exon_variant BLCA-US 10 122622425 122622425 single base substitution G A intron_variant BLCA-US 10 122622425 122622425 single base substitution G A synonymous_variant E235E 705G>A BLCA-US 10 122624668 122624668 single base substitution G C downstream_gene_variant BLCA-US 10 122624668 122624668 single base substitution G C exon_variant BLCA-US 10 122624668 122624668 single base substitution G C intron_variant BLCA-US 10 122624668 122624668 single base substitution G C missense_variant V16L 46G>C BLCA-US 10 122624668 122624668 single base substitution G C missense_variant V275L 823G>C BLCA-US 10 122624668 122624668 single base substitution G C upstream_gene_variant BLCA-US 10 122626260 122626260 single base substitution C A downstream_gene_variant BLCA-US 10 122626260 122626260 single base substitution C A exon_variant BLCA-US 10 122626260 122626260 single base substitution C A intron_variant BLCA-US 10 122626260 122626260 single base substitution C A synonymous_variant R133R 397C>A BLCA-US 10 122626260 122626260 single base substitution C A synonymous_variant R392R 1174C>A BLCA-US 10 122626260 122626260 single base substitution C A upstream_gene_variant BLCA-US 10 122637962 122637962 single base substitution C T 3_prime_UTR_variant BLCA-US 10 122637962 122637962 single base substitution C T exon_variant BLCA-US 10 122637962 122637962 single base substitution C T missense_variant L293F 877C>T BLCA-US 10 122637962 122637962 single base substitution C T missense_variant L552F 1654C>T BLCA-US 10 122637962 122637962 single base substitution C T upstream_gene_variant BLCA-US 10 122648591 122648591 single base substitution G A missense_variant G708E 2123G>A BLCA-US 10 122648591 122648591 single base substitution G A splice_region_variant BOCA-FR 10 122649559 122649559 single base substitution G A downstream_gene_variant BOCA-FR 10 122649559 122649559 single base substitution G A intron_variant BRCA-EU 10 122606080 122606080 single base substitution C G upstream_gene_variant BRCA-EU 10 122607380 122607380 single base substitution T A upstream_gene_variant BRCA-EU 10 122607390 122607390 single base substitution C T upstream_gene_variant BRCA-EU 10 122609369 122609369 single base substitution T A upstream_gene_variant BRCA-EU 10 122609801 122609801 single base substitution T C upstream_gene_variant BRCA-EU 10 122610000 122610000 single base substitution C A upstream_gene_variant BRCA-EU 10 122611147 122611147 single base substitution G C intron_variant BRCA-EU 10 122611147 122611147 single base substitution G C upstream_gene_variant BRCA-EU 10 122611726 122611726 single base substitution C T exon_variant BRCA-EU 10 122611726 122611726 single base substitution C T intron_variant BRCA-EU 10 122611726 122611726 single base substitution C T upstream_gene_variant BRCA-EU 10 122613185 122613185 single base substitution G C intron_variant BRCA-EU 10 122613534 122613534 single base substitution T A intron_variant BRCA-EU 10 122614003 122614003 single base substitution G A intron_variant BRCA-EU 10 122614250 122614250 single base substitution A G intron_variant BRCA-EU 10 122615302 122615302 single base substitution C G intron_variant BRCA-EU 10 122615879 122615879 single base substitution G C intron_variant BRCA-EU 10 122616163 122616163 single base substitution T G intron_variant BRCA-EU 10 122616167 122616167 single base substitution T A intron_variant BRCA-EU 10 122616410 122616410 single base substitution G A intron_variant BRCA-EU 10 122617136 122617136 single base substitution C G intron_variant BRCA-EU 10 122617136 122617136 single base substitution C G upstream_gene_variant BRCA-EU 10 122618474 122618474 single base substitution A G downstream_gene_variant BRCA-EU 10 122618474 122618474 single base substitution A G intron_variant BRCA-EU 10 122618474 122618474 single base substitution A G upstream_gene_variant BRCA-EU 10 122619730 122619730 single base substitution G C 5_prime_UTR_variant BRCA-EU 10 122619730 122619730 single base substitution G C downstream_gene_variant BRCA-EU 10 122619730 122619730 single base substitution G C exon_variant BRCA-EU 10 122619730 122619730 single base substitution G C intron_variant BRCA-EU 10 122619730 122619730 single base substitution G C missense_variant K154N 462G>C BRCA-EU 10 122619730 122619730 single base substitution G C upstream_gene_variant BRCA-EU 10 122619967 122619967 single base substitution C G downstream_gene_variant BRCA-EU 10 122619967 122619967 single base substitution C G intron_variant BRCA-EU 10 122619967 122619967 single base substitution C G upstream_gene_variant BRCA-EU 10 122620653 122620653 single base substitution G A downstream_gene_variant BRCA-EU 10 122620653 122620653 single base substitution G A intron_variant BRCA-EU 10 122620653 122620653 single base substitution G A upstream_gene_variant BRCA-EU 10 122621109 122621109 single base substitution G A downstream_gene_variant BRCA-EU 10 122621109 122621109 single base substitution G A intron_variant BRCA-EU 10 122621109 122621109 single base substitution G A upstream_gene_variant BRCA-EU 10 122621353 122621353 single base substitution G T downstream_gene_variant BRCA-EU 10 122621353 122621353 single base substitution G T intron_variant BRCA-EU 10 122621353 122621353 single base substitution G T upstream_gene_variant BRCA-EU 10 122624899 122624899 single base substitution G C downstream_gene_variant BRCA-EU 10 122624899 122624899 single base substitution G C intron_variant BRCA-EU 10 122624899 122624899 single base substitution G C upstream_gene_variant BRCA-EU 10 122625397 122625397 single base substitution C T downstream_gene_variant BRCA-EU 10 122625397 122625397 single base substitution C T intron_variant BRCA-EU 10 122625397 122625397 single base substitution C T upstream_gene_variant BRCA-EU 10 122626919 122626919 single base substitution G C downstream_gene_variant BRCA-EU 10 122626919 122626919 single base substitution G C intron_variant BRCA-EU 10 122626919 122626919 single base substitution G C upstream_gene_variant BRCA-EU 10 122627967 122627967 single base substitution T C downstream_gene_variant BRCA-EU 10 122627967 122627967 single base substitution T C intron_variant BRCA-EU 10 122627967 122627967 single base substitution T C upstream_gene_variant BRCA-EU 10 122630593 122630593 single base substitution G A intron_variant BRCA-EU 10 122631838 122631838 single base substitution T A intron_variant BRCA-EU 10 122633776 122633776 single base substitution A G intron_variant BRCA-EU 10 122633776 122633776 single base substitution A G upstream_gene_variant BRCA-EU 10 122635231 122635231 single base substitution G A intron_variant BRCA-EU 10 122635231 122635231 single base substitution G A upstream_gene_variant BRCA-EU 10 122635283 122635283 single base substitution C T intron_variant BRCA-EU 10 122635283 122635283 single base substitution C T upstream_gene_variant BRCA-EU 10 122635607 122635607 single base substitution C T intron_variant BRCA-EU 10 122635607 122635607 single base substitution C T upstream_gene_variant BRCA-EU 10 122636111 122636111 single base substitution G A intron_variant BRCA-EU 10 122636111 122636111 single base substitution G A upstream_gene_variant BRCA-EU 10 122636717 122636717 single base substitution A G intron_variant BRCA-EU 10 122636717 122636717 single base substitution A G upstream_gene_variant BRCA-EU 10 122641681 122641681 single base substitution A G downstream_gene_variant BRCA-EU 10 122641681 122641681 single base substitution A G intron_variant BRCA-EU 10 122641681 122641681 single base substitution A G upstream_gene_variant BRCA-EU 10 122641827 122641827 single base substitution C G downstream_gene_variant BRCA-EU 10 122641827 122641827 single base substitution C G intron_variant BRCA-EU 10 122641827 122641827 single base substitution C G upstream_gene_variant BRCA-EU 10 122641931 122641931 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 122641931 122641931 deletion of <=200bp T - intron_variant BRCA-EU 10 122641931 122641931 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 122644483 122644483 single base substitution C A downstream_gene_variant BRCA-EU 10 122644483 122644483 single base substitution C A intron_variant BRCA-EU 10 122644483 122644483 single base substitution C A upstream_gene_variant BRCA-EU 10 122644975 122644975 single base substitution G T downstream_gene_variant BRCA-EU 10 122644975 122644975 single base substitution G T intron_variant BRCA-EU 10 122644975 122644975 single base substitution G T upstream_gene_variant BRCA-EU 10 122645026 122645026 single base substitution G C downstream_gene_variant BRCA-EU 10 122645026 122645026 single base substitution G C intron_variant BRCA-EU 10 122645026 122645026 single base substitution G C upstream_gene_variant BRCA-EU 10 122647223 122647223 single base substitution G A downstream_gene_variant BRCA-EU 10 122647223 122647223 single base substitution G A intron_variant BRCA-EU 10 122648311 122648311 single base substitution T C downstream_gene_variant BRCA-EU 10 122648311 122648311 single base substitution T C intron_variant BRCA-EU 10 122648911 122648911 single base substitution G A exon_variant BRCA-EU 10 122648911 122648911 single base substitution G A intron_variant BRCA-EU 10 122649377 122649377 single base substitution G A exon_variant BRCA-EU 10 122649377 122649377 single base substitution G A intron_variant BRCA-EU 10 122651425 122651425 single base substitution A G downstream_gene_variant BRCA-EU 10 122651425 122651425 single base substitution A G intron_variant BRCA-EU 10 122652256 122652256 single base substitution A G downstream_gene_variant BRCA-EU 10 122652256 122652256 single base substitution A G intron_variant BRCA-EU 10 122652294 122652294 single base substitution T G downstream_gene_variant BRCA-EU 10 122652294 122652294 single base substitution T G intron_variant BRCA-EU 10 122652811 122652811 single base substitution A G downstream_gene_variant BRCA-EU 10 122652811 122652811 single base substitution A G intron_variant BRCA-EU 10 122654236 122654236 single base substitution A G downstream_gene_variant BRCA-EU 10 122654236 122654236 single base substitution A G intron_variant BRCA-EU 10 122654636 122654636 single base substitution T G intron_variant BRCA-EU 10 122654636 122654636 single base substitution T G upstream_gene_variant BRCA-EU 10 122655008 122655008 single base substitution G T intron_variant BRCA-EU 10 122655008 122655008 single base substitution G T upstream_gene_variant BRCA-EU 10 122655875 122655875 single base substitution G A intron_variant BRCA-EU 10 122655875 122655875 single base substitution G A upstream_gene_variant BRCA-EU 10 122656052 122656052 single base substitution C A intron_variant BRCA-EU 10 122656052 122656052 single base substitution C A upstream_gene_variant BRCA-EU 10 122656473 122656473 deletion of <=200bp C - intron_variant BRCA-EU 10 122656473 122656473 deletion of <=200bp C - upstream_gene_variant BRCA-EU 10 122656815 122656815 single base substitution C T intron_variant BRCA-EU 10 122656815 122656815 single base substitution C T upstream_gene_variant BRCA-EU 10 122657593 122657593 single base substitution T A intron_variant BRCA-EU 10 122657593 122657593 single base substitution T A upstream_gene_variant BRCA-EU 10 122659094 122659094 single base substitution A C intron_variant BRCA-EU 10 122659094 122659094 single base substitution A C upstream_gene_variant BRCA-EU 10 122659544 122659544 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 122659544 122659544 single base substitution C T exon_variant BRCA-EU 10 122659544 122659544 single base substitution C T missense_variant P840L 2519C>T BRCA-EU 10 122659544 122659544 single base substitution C T upstream_gene_variant BRCA-EU 10 122662715 122662715 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 122662715 122662715 single base substitution G A downstream_gene_variant BRCA-EU 10 122662715 122662715 single base substitution G A exon_variant BRCA-EU 10 122662715 122662715 single base substitution G A missense_variant D968N 2902G>A BRCA-EU 10 122662715 122662715 single base substitution G A upstream_gene_variant BRCA-EU 10 122662864 122662864 single base substitution C A downstream_gene_variant BRCA-EU 10 122662864 122662864 single base substitution C A intron_variant BRCA-EU 10 122662864 122662864 single base substitution C A upstream_gene_variant BRCA-EU 10 122663072 122663072 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 122663072 122663072 deletion of <=200bp A - intron_variant BRCA-EU 10 122663072 122663072 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 122664408 122664408 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 122664408 122664408 deletion of <=200bp T - intron_variant BRCA-EU 10 122664408 122664408 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 122665692 122665692 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 122665692 122665692 single base substitution C T downstream_gene_variant BRCA-EU 10 122665692 122665692 single base substitution C T intron_variant BRCA-EU 10 122665692 122665692 single base substitution C T upstream_gene_variant BRCA-EU 10 122665693 122665693 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 122665693 122665693 single base substitution G A downstream_gene_variant BRCA-EU 10 122665693 122665693 single base substitution G A intron_variant BRCA-EU 10 122665693 122665693 single base substitution G A upstream_gene_variant BRCA-EU 10 122667157 122667157 single base substitution T A downstream_gene_variant BRCA-EU 10 122667157 122667157 single base substitution T A exon_variant BRCA-EU 10 122667157 122667157 single base substitution T A intron_variant BRCA-EU 10 122667780 122667780 single base substitution T G downstream_gene_variant BRCA-EU 10 122667780 122667780 single base substitution T G exon_variant BRCA-EU 10 122667780 122667780 single base substitution T G intron_variant BRCA-EU 10 122668511 122668511 single base substitution A T 3_prime_UTR_variant BRCA-EU 10 122668511 122668511 single base substitution A T downstream_gene_variant BRCA-EU 10 122668511 122668511 single base substitution A T exon_variant BRCA-EU 10 122669357 122669357 single base substitution A G downstream_gene_variant BRCA-EU 10 122669806 122669806 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 122669850 122669850 single base substitution A G downstream_gene_variant BRCA-EU 10 122670109 122670109 single base substitution C G downstream_gene_variant BRCA-EU 10 122671979 122671979 single base substitution C G downstream_gene_variant BRCA-FR 10 122617136 122617136 single base substitution C G intron_variant BRCA-FR 10 122617136 122617136 single base substitution C G upstream_gene_variant BRCA-FR 10 122617922 122617922 single base substitution C T intron_variant BRCA-FR 10 122617922 122617922 single base substitution C T upstream_gene_variant BRCA-FR 10 122619730 122619730 single base substitution G C 5_prime_UTR_variant BRCA-FR 10 122619730 122619730 single base substitution G C downstream_gene_variant BRCA-FR 10 122619730 122619730 single base substitution G C exon_variant BRCA-FR 10 122619730 122619730 single base substitution G C intron_variant BRCA-FR 10 122619730 122619730 single base substitution G C missense_variant K154N 462G>C BRCA-FR 10 122619730 122619730 single base substitution G C upstream_gene_variant BRCA-FR 10 122630593 122630593 single base substitution G A intron_variant BRCA-FR 10 122635607 122635607 single base substitution C T intron_variant BRCA-FR 10 122635607 122635607 single base substitution C T upstream_gene_variant BRCA-FR 10 122654636 122654636 single base substitution T G intron_variant BRCA-FR 10 122654636 122654636 single base substitution T G upstream_gene_variant BRCA-FR 10 122655875 122655875 single base substitution G A intron_variant BRCA-FR 10 122655875 122655875 single base substitution G A upstream_gene_variant BRCA-FR 10 122656815 122656815 single base substitution C T intron_variant BRCA-FR 10 122656815 122656815 single base substitution C T upstream_gene_variant BRCA-FR 10 122665459 122665459 single base substitution C A 3_prime_UTR_variant BRCA-FR 10 122665459 122665459 single base substitution C A downstream_gene_variant BRCA-FR 10 122665459 122665459 single base substitution C A exon_variant BRCA-FR 10 122665459 122665459 single base substitution C A synonymous_variant V1121V 3363C>A BRCA-FR 10 122665459 122665459 single base substitution C A upstream_gene_variant BRCA-FR 10 122667049 122667049 single base substitution C T downstream_gene_variant BRCA-FR 10 122667049 122667049 single base substitution C T exon_variant BRCA-FR 10 122667049 122667049 single base substitution C T intron_variant BRCA-UK 10 122611726 122611726 single base substitution C T exon_variant BRCA-UK 10 122611726 122611726 single base substitution C T intron_variant BRCA-UK 10 122611726 122611726 single base substitution C T upstream_gene_variant BRCA-UK 10 122670600 122670600 single base substitution G C downstream_gene_variant BRCA-US 10 122618231 122618231 single base substitution A G 5_prime_UTR_variant BRCA-US 10 122618231 122618231 single base substitution A G exon_variant BRCA-US 10 122618231 122618231 single base substitution A G intron_variant BRCA-US 10 122618231 122618231 single base substitution A G missense_variant N92S 275A>G BRCA-US 10 122618231 122618231 single base substitution A G upstream_gene_variant BRCA-US 10 122622406 122622406 single base substitution A G 5_prime_UTR_variant BRCA-US 10 122622406 122622406 single base substitution A G downstream_gene_variant BRCA-US 10 122622406 122622406 single base substitution A G exon_variant BRCA-US 10 122622406 122622406 single base substitution A G intron_variant BRCA-US 10 122622406 122622406 single base substitution A G missense_variant K229R 686A>G BRCA-US 10 122643389 122643389 single base substitution A G 3_prime_UTR_variant BRCA-US 10 122643389 122643389 single base substitution A G downstream_gene_variant BRCA-US 10 122643389 122643389 single base substitution A G exon_variant BRCA-US 10 122643389 122643389 single base substitution A G missense_variant I613V 1837A>G BRCA-US 10 122643389 122643389 single base substitution A G upstream_gene_variant BRCA-US 10 122646224 122646234 deletion of <=200bp AATCTGAACTT - 3_prime_UTR_variant BRCA-US 10 122646224 122646234 deletion of <=200bp AATCTGAACTT - downstream_gene_variant BRCA-US 10 122646224 122646234 deletion of <=200bp AATCTGAACTT - exon_variant BRCA-US 10 122646224 122646234 deletion of <=200bp AATCTGAACTT - frameshift_variant KSEL666 BRCA-US 10 122648628 122648628 single base substitution T G 3_prime_UTR_variant BRCA-US 10 122648628 122648628 single base substitution T G exon_variant BRCA-US 10 122648628 122648628 single base substitution T G synonymous_variant G720G 2160T>G BRCA-US 10 122649430 122649430 single base substitution G C 3_prime_UTR_variant BRCA-US 10 122649430 122649430 single base substitution G C exon_variant BRCA-US 10 122649430 122649430 single base substitution G C missense_variant W751S 2252G>C BRCA-US 10 122668442 122668442 single base substitution A C 3_prime_UTR_variant BRCA-US 10 122668442 122668442 single base substitution A C downstream_gene_variant BRCA-US 10 122668442 122668442 single base substitution A C exon_variant BTCA-JP 10 122618263 122618263 single base substitution G A 5_prime_UTR_variant BTCA-JP 10 122618263 122618263 single base substitution G A exon_variant BTCA-JP 10 122618263 122618263 single base substitution G A intron_variant BTCA-JP 10 122618263 122618263 single base substitution G A missense_variant G103R 307G>A BTCA-JP 10 122618263 122618263 single base substitution G A upstream_gene_variant BTCA-JP 10 122619753 122619753 single base substitution T A 5_prime_UTR_variant BTCA-JP 10 122619753 122619753 single base substitution T A downstream_gene_variant BTCA-JP 10 122619753 122619753 single base substitution T A exon_variant BTCA-JP 10 122619753 122619753 single base substitution T A intron_variant BTCA-JP 10 122619753 122619753 single base substitution T A missense_variant L162H 485T>A BTCA-JP 10 122619753 122619753 single base substitution T A upstream_gene_variant BTCA-JP 10 122622151 122622151 single base substitution A C downstream_gene_variant BTCA-JP 10 122622151 122622151 single base substitution A C exon_variant BTCA-JP 10 122622151 122622151 single base substitution A C intron_variant BTCA-JP 10 122640469 122640469 deletion of <=200bp T - downstream_gene_variant BTCA-JP 10 122640469 122640469 deletion of <=200bp T - intron_variant BTCA-JP 10 122640469 122640469 deletion of <=200bp T - upstream_gene_variant BTCA-JP 10 122643797 122643797 single base substitution T C downstream_gene_variant BTCA-JP 10 122643797 122643797 single base substitution T C intron_variant BTCA-JP 10 122643797 122643797 single base substitution T C upstream_gene_variant BTCA-JP 10 122648528 122648528 single base substitution T G intron_variant BTCA-JP 10 122648768 122648768 single base substitution G T exon_variant BTCA-JP 10 122648768 122648768 single base substitution G T intron_variant BTCA-JP 10 122660567 122660567 single base substitution G A 3_prime_UTR_variant BTCA-JP 10 122660567 122660567 single base substitution G A exon_variant BTCA-JP 10 122660567 122660567 single base substitution G A missense_variant E882K 2644G>A BTCA-JP 10 122660567 122660567 single base substitution G A upstream_gene_variant BTCA-JP 10 122664350 122664351 deletion of <=200bp TC - downstream_gene_variant BTCA-JP 10 122664350 122664351 deletion of <=200bp TC - intron_variant BTCA-JP 10 122664350 122664351 deletion of <=200bp TC - upstream_gene_variant BTCA-JP 10 122665475 122665475 single base substitution G A 3_prime_UTR_variant BTCA-JP 10 122665475 122665475 single base substitution G A downstream_gene_variant BTCA-JP 10 122665475 122665475 single base substitution G A exon_variant BTCA-JP 10 122665475 122665475 single base substitution G A missense_variant A1127T 3379G>A BTCA-JP 10 122665475 122665475 single base substitution G A upstream_gene_variant CESC-US 10 122633397 122633397 single base substitution G C 3_prime_UTR_variant CESC-US 10 122633397 122633397 single base substitution G C exon_variant CESC-US 10 122633397 122633397 single base substitution G C synonymous_variant L247L 741G>C CESC-US 10 122633397 122633397 single base substitution G C synonymous_variant L506L 1518G>C CESC-US 10 122664255 122664255 single base substitution C T 3_prime_UTR_variant CESC-US 10 122664255 122664255 single base substitution C T downstream_gene_variant CESC-US 10 122664255 122664255 single base substitution C T exon_variant CESC-US 10 122664255 122664255 single base substitution C T intron_variant CESC-US 10 122664255 122664255 single base substitution C T missense_variant S1042L 3125C>T CESC-US 10 122664255 122664255 single base substitution C T upstream_gene_variant CESC-US 10 122668664 122668664 single base substitution C T 3_prime_UTR_variant CESC-US 10 122668664 122668664 single base substitution C T downstream_gene_variant CESC-US 10 122668664 122668664 single base substitution C T exon_variant CESC-US 10 122668850 122668850 single base substitution G C 3_prime_UTR_variant CESC-US 10 122668850 122668850 single base substitution G C downstream_gene_variant CESC-US 10 122668850 122668850 single base substitution G C exon_variant CLLE-ES 10 122625691 122625691 single base substitution A T downstream_gene_variant CLLE-ES 10 122625691 122625691 single base substitution A T intron_variant CLLE-ES 10 122625691 122625691 single base substitution A T upstream_gene_variant CLLE-ES 10 122632414 122632414 single base substitution T C intron_variant CLLE-ES 10 122634543 122634543 single base substitution G A intron_variant CLLE-ES 10 122634543 122634543 single base substitution G A upstream_gene_variant CLLE-ES 10 122635569 122635569 single base substitution C T intron_variant CLLE-ES 10 122635569 122635569 single base substitution C T upstream_gene_variant CLLE-ES 10 122649908 122649908 single base substitution T A downstream_gene_variant CLLE-ES 10 122649908 122649908 single base substitution T A intron_variant COAD-US 10 122625220 122625220 single base substitution T C downstream_gene_variant COAD-US 10 122625220 122625220 single base substitution T C exon_variant COAD-US 10 122625220 122625220 single base substitution T C intron_variant COAD-US 10 122625220 122625220 single base substitution T C missense_variant Y320H 958T>C COAD-US 10 122625220 122625220 single base substitution T C missense_variant Y61H 181T>C COAD-US 10 122625220 122625220 single base substitution T C upstream_gene_variant COAD-US 10 122633421 122633421 single base substitution C T 3_prime_UTR_variant COAD-US 10 122633421 122633421 single base substitution C T exon_variant COAD-US 10 122633421 122633421 single base substitution C T synonymous_variant H255H 765C>T COAD-US 10 122633421 122633421 single base substitution C T synonymous_variant H514H 1542C>T COAD-US 10 122640355 122640355 single base substitution C T 3_prime_UTR_variant COAD-US 10 122640355 122640355 single base substitution C T exon_variant COAD-US 10 122640355 122640355 single base substitution C T missense_variant R302C 904C>T COAD-US 10 122640355 122640355 single base substitution C T missense_variant R561C 1681C>T COAD-US 10 122640355 122640355 single base substitution C T upstream_gene_variant COAD-US 10 122643322 122643322 single base substitution A G 3_prime_UTR_variant COAD-US 10 122643322 122643322 single base substitution A G downstream_gene_variant COAD-US 10 122643322 122643322 single base substitution A G exon_variant COAD-US 10 122643322 122643322 single base substitution A G synonymous_variant K590K 1770A>G COAD-US 10 122643322 122643322 single base substitution A G upstream_gene_variant COAD-US 10 122649410 122649410 single base substitution A G 3_prime_UTR_variant COAD-US 10 122649410 122649410 single base substitution A G exon_variant COAD-US 10 122649410 122649410 single base substitution A G synonymous_variant G744G 2232A>G COAD-US 10 122650306 122650306 single base substitution A G 3_prime_UTR_variant COAD-US 10 122650306 122650306 single base substitution A G downstream_gene_variant COAD-US 10 122650306 122650306 single base substitution A G intron_variant COAD-US 10 122650306 122650306 single base substitution A G missense_variant K808E 2422A>G COAD-US 10 122661812 122661812 single base substitution C T 3_prime_UTR_variant COAD-US 10 122661812 122661812 single base substitution C T exon_variant COAD-US 10 122661812 122661812 single base substitution C T stop_gained Q911* 2731C>T COAD-US 10 122661812 122661812 single base substitution C T upstream_gene_variant COAD-US 10 122662745 122662745 single base substitution G T downstream_gene_variant COAD-US 10 122662745 122662745 single base substitution G T splice_donor_variant COAD-US 10 122662745 122662745 single base substitution G T upstream_gene_variant COAD-US 10 122663585 122663585 single base substitution G A 3_prime_UTR_variant COAD-US 10 122663585 122663585 single base substitution G A downstream_gene_variant COAD-US 10 122663585 122663585 single base substitution G A exon_variant COAD-US 10 122663585 122663585 single base substitution G A synonymous_variant L986L 2958G>A COAD-US 10 122663585 122663585 single base substitution G A upstream_gene_variant COAD-US 10 122664871 122664871 single base substitution C T 3_prime_UTR_variant COAD-US 10 122664871 122664871 single base substitution C T downstream_gene_variant COAD-US 10 122664871 122664871 single base substitution C T exon_variant COAD-US 10 122664871 122664871 single base substitution C T synonymous_variant D1078D 3234C>T COAD-US 10 122664871 122664871 single base substitution C T upstream_gene_variant COAD-US 10 122665414 122665414 single base substitution C T 3_prime_UTR_variant COAD-US 10 122665414 122665414 single base substitution C T downstream_gene_variant COAD-US 10 122665414 122665414 single base substitution C T exon_variant COAD-US 10 122665414 122665414 single base substitution C T synonymous_variant A1106A 3318C>T COAD-US 10 122665414 122665414 single base substitution C T upstream_gene_variant COAD-US 10 122665427 122665427 single base substitution C T 3_prime_UTR_variant COAD-US 10 122665427 122665427 single base substitution C T downstream_gene_variant COAD-US 10 122665427 122665427 single base substitution C T exon_variant COAD-US 10 122665427 122665427 single base substitution C T missense_variant R1111W 3331C>T COAD-US 10 122665427 122665427 single base substitution C T upstream_gene_variant COAD-US 10 122668142 122668142 single base substitution C A 3_prime_UTR_variant COAD-US 10 122668142 122668142 single base substitution C A downstream_gene_variant COAD-US 10 122668142 122668142 single base substitution C A exon_variant COAD-US 10 122668142 122668142 single base substitution C A missense_variant L1198I 3592C>A COCA-CN 10 122608501 122608501 single base substitution A G upstream_gene_variant COCA-CN 10 122611110 122611110 single base substitution T G intron_variant COCA-CN 10 122611110 122611110 single base substitution T G upstream_gene_variant COCA-CN 10 122614323 122614323 single base substitution G A intron_variant COCA-CN 10 122618142 122618142 single base substitution C A intron_variant COCA-CN 10 122618142 122618142 single base substitution C A upstream_gene_variant COCA-CN 10 122621646 122621646 single base substitution G T downstream_gene_variant COCA-CN 10 122621646 122621646 single base substitution G T intron_variant COCA-CN 10 122621646 122621646 single base substitution G T upstream_gene_variant COCA-CN 10 122623484 122623484 single base substitution T G downstream_gene_variant COCA-CN 10 122623484 122623484 single base substitution T G intron_variant COCA-CN 10 122623484 122623484 single base substitution T G upstream_gene_variant COCA-CN 10 122624527 122624527 single base substitution C A downstream_gene_variant COCA-CN 10 122624527 122624527 single base substitution C A intron_variant COCA-CN 10 122624527 122624527 single base substitution C A upstream_gene_variant COCA-CN 10 122626211 122626211 single base substitution G A downstream_gene_variant COCA-CN 10 122626211 122626211 single base substitution G A exon_variant COCA-CN 10 122626211 122626211 single base substitution G A intron_variant COCA-CN 10 122626211 122626211 single base substitution G A synonymous_variant V116V 348G>A COCA-CN 10 122626211 122626211 single base substitution G A synonymous_variant V375V 1125G>A COCA-CN 10 122626211 122626211 single base substitution G A upstream_gene_variant COCA-CN 10 122629059 122629059 single base substitution T G downstream_gene_variant COCA-CN 10 122629059 122629059 single base substitution T G intron_variant COCA-CN 10 122633252 122633252 single base substitution T G intron_variant COCA-CN 10 122633349 122633349 single base substitution A T splice_acceptor_variant COCA-CN 10 122643421 122643421 single base substitution T G downstream_gene_variant COCA-CN 10 122643421 122643421 single base substitution T G intron_variant COCA-CN 10 122643421 122643421 single base substitution T G upstream_gene_variant COCA-CN 10 122646113 122646113 single base substitution C T downstream_gene_variant COCA-CN 10 122646113 122646113 single base substitution C T intron_variant COCA-CN 10 122647449 122647449 single base substitution T G downstream_gene_variant COCA-CN 10 122647449 122647449 single base substitution T G intron_variant COCA-CN 10 122653391 122653391 single base substitution A T downstream_gene_variant COCA-CN 10 122653391 122653391 single base substitution A T intron_variant COCA-CN 10 122659578 122659578 single base substitution C A 3_prime_UTR_variant COCA-CN 10 122659578 122659578 single base substitution C A exon_variant COCA-CN 10 122659578 122659578 single base substitution C A synonymous_variant A851A 2553C>A COCA-CN 10 122659578 122659578 single base substitution C A upstream_gene_variant COCA-CN 10 122659595 122659595 single base substitution C T 3_prime_UTR_variant COCA-CN 10 122659595 122659595 single base substitution C T exon_variant COCA-CN 10 122659595 122659595 single base substitution C T missense_variant A857V 2570C>T COCA-CN 10 122659595 122659595 single base substitution C T upstream_gene_variant COCA-CN 10 122661832 122661832 single base substitution A G splice_region_variant COCA-CN 10 122661832 122661832 single base substitution A G upstream_gene_variant COCA-CN 10 122663530 122663530 single base substitution C T downstream_gene_variant COCA-CN 10 122663530 122663530 single base substitution C T intron_variant COCA-CN 10 122663530 122663530 single base substitution C T upstream_gene_variant COCA-CN 10 122664312 122664312 single base substitution G T 3_prime_UTR_variant COCA-CN 10 122664312 122664312 single base substitution G T downstream_gene_variant COCA-CN 10 122664312 122664312 single base substitution G T exon_variant COCA-CN 10 122664312 122664312 single base substitution G T intron_variant COCA-CN 10 122664312 122664312 single base substitution G T missense_variant G1061V 3182G>T COCA-CN 10 122664312 122664312 single base substitution G T upstream_gene_variant COCA-CN 10 122666277 122666277 single base substitution C A 3_prime_UTR_variant COCA-CN 10 122666277 122666277 single base substitution C A downstream_gene_variant COCA-CN 10 122666277 122666277 single base substitution C A intron_variant COCA-CN 10 122666277 122666277 single base substitution C A upstream_gene_variant COCA-CN 10 122671341 122671341 single base substitution C A downstream_gene_variant COCA-CN 10 122671447 122671447 single base substitution C G downstream_gene_variant COCA-CN 10 122671536 122671536 single base substitution T C downstream_gene_variant COCA-CN 10 122671685 122671685 single base substitution G A downstream_gene_variant COCA-CN 10 122671705 122671705 single base substitution C T downstream_gene_variant COCA-CN 10 122671707 122671707 single base substitution G C downstream_gene_variant COCA-CN 10 122671952 122671952 single base substitution G C downstream_gene_variant COCA-CN 10 122672045 122672045 single base substitution G A downstream_gene_variant EOPC-DE 10 122621269 122621269 single base substitution C T downstream_gene_variant EOPC-DE 10 122621269 122621269 single base substitution C T intron_variant EOPC-DE 10 122621269 122621269 single base substitution C T upstream_gene_variant EOPC-DE 10 122625955 122625955 single base substitution C A downstream_gene_variant EOPC-DE 10 122625955 122625955 single base substitution C A intron_variant EOPC-DE 10 122625955 122625955 single base substitution C A upstream_gene_variant EOPC-DE 10 122628235 122628235 single base substitution C G downstream_gene_variant EOPC-DE 10 122628235 122628235 single base substitution C G exon_variant EOPC-DE 10 122628235 122628235 single base substitution C G intron_variant ESAD-UK 10 122610063 122610063 single base substitution C T upstream_gene_variant ESAD-UK 10 122610770 122610770 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 10 122610770 122610770 single base substitution A T upstream_gene_variant ESAD-UK 10 122610933 122610933 single base substitution A T exon_variant ESAD-UK 10 122610933 122610933 single base substitution A T initiator_codon_variant M1L 1A>T ESAD-UK 10 122610933 122610933 single base substitution A T upstream_gene_variant ESAD-UK 10 122611030 122611030 single base substitution G A 5_prime_UTR_variant ESAD-UK 10 122611030 122611030 single base substitution G A exon_variant ESAD-UK 10 122611030 122611030 single base substitution G A intron_variant ESAD-UK 10 122611030 122611030 single base substitution G A upstream_gene_variant ESAD-UK 10 122613888 122613888 single base substitution A C intron_variant ESAD-UK 10 122616243 122616243 insertion of <=200bp - AT intron_variant ESAD-UK 10 122616483 122616483 single base substitution G T intron_variant ESAD-UK 10 122617342 122617342 single base substitution C T intron_variant ESAD-UK 10 122617342 122617342 single base substitution C T upstream_gene_variant ESAD-UK 10 122618523 122618523 single base substitution T C downstream_gene_variant ESAD-UK 10 122618523 122618523 single base substitution T C intron_variant ESAD-UK 10 122618523 122618523 single base substitution T C upstream_gene_variant ESAD-UK 10 122622853 122622853 single base substitution G A downstream_gene_variant ESAD-UK 10 122622853 122622853 single base substitution G A intron_variant ESAD-UK 10 122623120 122623120 single base substitution G A downstream_gene_variant ESAD-UK 10 122623120 122623120 single base substitution G A intron_variant ESAD-UK 10 122624701 122624701 single base substitution C T downstream_gene_variant ESAD-UK 10 122624701 122624701 single base substitution C T exon_variant ESAD-UK 10 122624701 122624701 single base substitution C T intron_variant ESAD-UK 10 122624701 122624701 single base substitution C T missense_variant R27C 79C>T ESAD-UK 10 122624701 122624701 single base substitution C T missense_variant R286C 856C>T ESAD-UK 10 122624701 122624701 single base substitution C T upstream_gene_variant ESAD-UK 10 122627621 122627621 single base substitution A G downstream_gene_variant ESAD-UK 10 122627621 122627621 single base substitution A G intron_variant ESAD-UK 10 122627621 122627621 single base substitution A G upstream_gene_variant ESAD-UK 10 122627652 122627652 single base substitution C T downstream_gene_variant ESAD-UK 10 122627652 122627652 single base substitution C T intron_variant ESAD-UK 10 122627652 122627652 single base substitution C T upstream_gene_variant ESAD-UK 10 122628487 122628487 single base substitution T C downstream_gene_variant ESAD-UK 10 122628487 122628487 single base substitution T C intron_variant ESAD-UK 10 122630631 122630631 single base substitution A T intron_variant ESAD-UK 10 122632131 122632131 single base substitution G C intron_variant ESAD-UK 10 122633165 122633165 deletion of <=200bp T - intron_variant ESAD-UK 10 122636260 122636260 single base substitution A G intron_variant ESAD-UK 10 122636260 122636260 single base substitution A G upstream_gene_variant ESAD-UK 10 122639299 122639299 single base substitution G C exon_variant ESAD-UK 10 122639299 122639299 single base substitution G C intron_variant ESAD-UK 10 122639301 122639301 single base substitution G A exon_variant ESAD-UK 10 122639301 122639301 single base substitution G A intron_variant ESAD-UK 10 122640030 122640030 single base substitution G A exon_variant ESAD-UK 10 122640030 122640030 single base substitution G A intron_variant ESAD-UK 10 122640030 122640030 single base substitution G A upstream_gene_variant ESAD-UK 10 122640388 122640388 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 122640388 122640388 single base substitution G A downstream_gene_variant ESAD-UK 10 122640388 122640388 single base substitution G A exon_variant ESAD-UK 10 122640388 122640388 single base substitution G A missense_variant E572K 1714G>A ESAD-UK 10 122640388 122640388 single base substitution G A upstream_gene_variant ESAD-UK 10 122643062 122643062 single base substitution C A downstream_gene_variant ESAD-UK 10 122643062 122643062 single base substitution C A intron_variant ESAD-UK 10 122643062 122643062 single base substitution C A upstream_gene_variant ESAD-UK 10 122643983 122643983 single base substitution G A downstream_gene_variant ESAD-UK 10 122643983 122643983 single base substitution G A intron_variant ESAD-UK 10 122643983 122643983 single base substitution G A upstream_gene_variant ESAD-UK 10 122644784 122644785 deletion of <=200bp TA - downstream_gene_variant ESAD-UK 10 122644784 122644785 deletion of <=200bp TA - intron_variant ESAD-UK 10 122644784 122644785 deletion of <=200bp TA - upstream_gene_variant ESAD-UK 10 122645657 122645657 single base substitution T G downstream_gene_variant ESAD-UK 10 122645657 122645657 single base substitution T G intron_variant ESAD-UK 10 122647157 122647157 single base substitution T C downstream_gene_variant ESAD-UK 10 122647157 122647157 single base substitution T C intron_variant ESAD-UK 10 122648897 122648897 single base substitution C G exon_variant ESAD-UK 10 122648897 122648897 single base substitution C G intron_variant ESAD-UK 10 122654008 122654008 single base substitution C T downstream_gene_variant ESAD-UK 10 122654008 122654008 single base substitution C T intron_variant ESAD-UK 10 122656040 122656040 insertion of <=200bp - CA intron_variant ESAD-UK 10 122656040 122656040 insertion of <=200bp - CA upstream_gene_variant ESAD-UK 10 122656478 122656478 single base substitution G A intron_variant ESAD-UK 10 122656478 122656478 single base substitution G A upstream_gene_variant ESAD-UK 10 122657203 122657203 single base substitution G A intron_variant ESAD-UK 10 122657203 122657203 single base substitution G A upstream_gene_variant ESAD-UK 10 122658532 122658532 single base substitution G C intron_variant ESAD-UK 10 122658532 122658532 single base substitution G C upstream_gene_variant ESAD-UK 10 122659294 122659294 single base substitution C A intron_variant ESAD-UK 10 122659294 122659294 single base substitution C A upstream_gene_variant ESAD-UK 10 122659440 122659440 single base substitution C T exon_variant ESAD-UK 10 122659440 122659440 single base substitution C T intron_variant ESAD-UK 10 122659440 122659440 single base substitution C T upstream_gene_variant ESAD-UK 10 122660760 122660760 single base substitution G A intron_variant ESAD-UK 10 122660760 122660760 single base substitution G A upstream_gene_variant ESAD-UK 10 122666186 122666186 single base substitution G T 3_prime_UTR_variant ESAD-UK 10 122666186 122666186 single base substitution G T downstream_gene_variant ESAD-UK 10 122666186 122666186 single base substitution G T intron_variant ESAD-UK 10 122666186 122666186 single base substitution G T upstream_gene_variant ESAD-UK 10 122666759 122666759 single base substitution A C downstream_gene_variant ESAD-UK 10 122666759 122666759 single base substitution A C intron_variant ESAD-UK 10 122666759 122666759 single base substitution A C upstream_gene_variant ESAD-UK 10 122668841 122668841 single base substitution G C 3_prime_UTR_variant ESAD-UK 10 122668841 122668841 single base substitution G C downstream_gene_variant ESAD-UK 10 122668841 122668841 single base substitution G C exon_variant ESCA-CN 10 122646070 122646070 single base substitution G C downstream_gene_variant ESCA-CN 10 122646070 122646070 single base substitution G C intron_variant ESCA-CN 10 122661725 122661725 single base substitution G A intron_variant ESCA-CN 10 122661725 122661725 single base substitution G A upstream_gene_variant ESCA-CN 10 122664872 122664872 single base substitution G A 3_prime_UTR_variant ESCA-CN 10 122664872 122664872 single base substitution G A downstream_gene_variant ESCA-CN 10 122664872 122664872 single base substitution G A exon_variant ESCA-CN 10 122664872 122664872 single base substitution G A missense_variant A1079T 3235G>A ESCA-CN 10 122664872 122664872 single base substitution G A upstream_gene_variant GBM-US 10 122622305 122622305 single base substitution A G 5_prime_UTR_variant GBM-US 10 122622305 122622305 single base substitution A G downstream_gene_variant GBM-US 10 122622305 122622305 single base substitution A G exon_variant GBM-US 10 122622305 122622305 single base substitution A G intron_variant GBM-US 10 122622305 122622305 single base substitution A G synonymous_variant S195S 585A>G GBM-US 10 122645345 122645345 single base substitution A G 3_prime_UTR_variant GBM-US 10 122645345 122645345 single base substitution A G downstream_gene_variant GBM-US 10 122645345 122645345 single base substitution A G exon_variant GBM-US 10 122645345 122645345 single base substitution A G missense_variant N623S 1868A>G GBM-US 10 122645345 122645345 single base substitution A G upstream_gene_variant GBM-US 10 122649467 122649467 single base substitution T C 3_prime_UTR_variant GBM-US 10 122649467 122649467 single base substitution T C exon_variant GBM-US 10 122649467 122649467 single base substitution T C synonymous_variant N763N 2289T>C KIRC-US 10 122624668 122624668 single base substitution G C downstream_gene_variant KIRC-US 10 122624668 122624668 single base substitution G C exon_variant KIRC-US 10 122624668 122624668 single base substitution G C intron_variant KIRC-US 10 122624668 122624668 single base substitution G C missense_variant V16L 46G>C KIRC-US 10 122624668 122624668 single base substitution G C missense_variant V275L 823G>C KIRC-US 10 122624668 122624668 single base substitution G C upstream_gene_variant KIRC-US 10 122661797 122661797 single base substitution G T 3_prime_UTR_variant KIRC-US 10 122661797 122661797 single base substitution G T exon_variant KIRC-US 10 122661797 122661797 single base substitution G T stop_gained E906* 2716G>T KIRC-US 10 122661797 122661797 single base substitution G T upstream_gene_variant KIRC-US 10 122663626 122663626 single base substitution G A 3_prime_UTR_variant KIRC-US 10 122663626 122663626 single base substitution G A downstream_gene_variant KIRC-US 10 122663626 122663626 single base substitution G A exon_variant KIRC-US 10 122663626 122663626 single base substitution G A missense_variant C1000Y 2999G>A KIRC-US 10 122663626 122663626 single base substitution G A upstream_gene_variant KIRP-US 10 122664157 122664157 single base substitution G A downstream_gene_variant KIRP-US 10 122664157 122664157 single base substitution G A intron_variant KIRP-US 10 122664157 122664157 single base substitution G A splice_acceptor_variant KIRP-US 10 122664157 122664157 single base substitution G A splice_region_variant KIRP-US 10 122664157 122664157 single base substitution G A upstream_gene_variant KIRP-US 10 122665439 122665439 single base substitution C A 3_prime_UTR_variant KIRP-US 10 122665439 122665439 single base substitution C A downstream_gene_variant KIRP-US 10 122665439 122665439 single base substitution C A exon_variant KIRP-US 10 122665439 122665439 single base substitution C A missense_variant H1115N 3343C>A KIRP-US 10 122665439 122665439 single base substitution C A upstream_gene_variant KIRP-US 10 122665493 122665493 single base substitution T A 3_prime_UTR_variant KIRP-US 10 122665493 122665493 single base substitution T A downstream_gene_variant KIRP-US 10 122665493 122665493 single base substitution T A exon_variant KIRP-US 10 122665493 122665493 single base substitution T A missense_variant S1133T 3397T>A KIRP-US 10 122665493 122665493 single base substitution T A upstream_gene_variant LAML-KR 10 122607171 122607171 single base substitution C T upstream_gene_variant LAML-KR 10 122646113 122646113 single base substitution C T downstream_gene_variant LAML-KR 10 122646113 122646113 single base substitution C T intron_variant LAML-KR 10 122650193 122650193 single base substitution C T downstream_gene_variant LAML-KR 10 122650193 122650193 single base substitution C T intron_variant LAML-KR 10 122653433 122653433 single base substitution C T downstream_gene_variant LAML-KR 10 122653433 122653433 single base substitution C T intron_variant LAML-KR 10 122653685 122653685 single base substitution A G downstream_gene_variant LAML-KR 10 122653685 122653685 single base substitution A G intron_variant LAML-KR 10 122664967 122664967 single base substitution C T downstream_gene_variant LAML-KR 10 122664967 122664967 single base substitution C T exon_variant LAML-KR 10 122664967 122664967 single base substitution C T intron_variant LAML-KR 10 122664967 122664967 single base substitution C T upstream_gene_variant LAML-KR 10 122671476 122671476 single base substitution G C downstream_gene_variant LAML-KR 10 122671481 122671481 single base substitution C A downstream_gene_variant LAML-KR 10 122672860 122672860 single base substitution A C downstream_gene_variant LAML-KR 10 122672947 122672947 single base substitution C T downstream_gene_variant LAML-KR 10 122673199 122673199 single base substitution A G downstream_gene_variant LAML-KR 10 122674035 122674035 single base substitution A G downstream_gene_variant LGG-US 10 122664218 122664218 single base substitution G C 3_prime_UTR_variant LGG-US 10 122664218 122664218 single base substitution G C downstream_gene_variant LGG-US 10 122664218 122664218 single base substitution G C exon_variant LGG-US 10 122664218 122664218 single base substitution G C intron_variant LGG-US 10 122664218 122664218 single base substitution G C missense_variant D1030H 3088G>C LGG-US 10 122664218 122664218 single base substitution G C upstream_gene_variant LIAD-FR 10 122633432 122633432 single base substitution T G 3_prime_UTR_variant LIAD-FR 10 122633432 122633432 single base substitution T G exon_variant LIAD-FR 10 122633432 122633432 single base substitution T G missense_variant V259G 776T>G LIAD-FR 10 122633432 122633432 single base substitution T G missense_variant V518G 1553T>G LICA-CN 10 122624623 122624623 single base substitution A T downstream_gene_variant LICA-CN 10 122624623 122624623 single base substitution A T exon_variant LICA-CN 10 122624623 122624623 single base substitution A T initiator_codon_variant M1L 1A>T LICA-CN 10 122624623 122624623 single base substitution A T intron_variant LICA-CN 10 122624623 122624623 single base substitution A T missense_variant M260L 778A>T LICA-CN 10 122624623 122624623 single base substitution A T upstream_gene_variant LICA-CN 10 122633354 122633354 single base substitution C T exon_variant LICA-CN 10 122633354 122633354 single base substitution C T missense_variant T233I 698C>T LICA-CN 10 122633354 122633354 single base substitution C T missense_variant T492I 1475C>T LICA-CN 10 122646209 122646209 single base substitution A T 3_prime_UTR_variant LICA-CN 10 122646209 122646209 single base substitution A T downstream_gene_variant LICA-CN 10 122646209 122646209 single base substitution A T exon_variant LICA-CN 10 122646209 122646209 single base substitution A T missense_variant Q661L 1982A>T LICA-CN 10 122650382 122650382 single base substitution A G 3_prime_UTR_variant LICA-CN 10 122650382 122650382 single base substitution A G downstream_gene_variant LICA-CN 10 122650382 122650382 single base substitution A G intron_variant LICA-CN 10 122650382 122650382 single base substitution A G missense_variant D833G 2498A>G LICA-CN 10 122663595 122663595 single base substitution A T 3_prime_UTR_variant LICA-CN 10 122663595 122663595 single base substitution A T downstream_gene_variant LICA-CN 10 122663595 122663595 single base substitution A T exon_variant LICA-CN 10 122663595 122663595 single base substitution A T stop_gained K990* 2968A>T LICA-CN 10 122663595 122663595 single base substitution A T upstream_gene_variant LICA-FR 10 122606780 122606780 single base substitution C T upstream_gene_variant LICA-FR 10 122606783 122606783 single base substitution A G upstream_gene_variant LICA-FR 10 122606854 122606854 single base substitution C T upstream_gene_variant LICA-FR 10 122619178 122619178 single base substitution G A downstream_gene_variant LICA-FR 10 122619178 122619178 single base substitution G A intron_variant LICA-FR 10 122619178 122619178 single base substitution G A upstream_gene_variant LICA-FR 10 122622403 122622403 single base substitution T C 5_prime_UTR_variant LICA-FR 10 122622403 122622403 single base substitution T C downstream_gene_variant LICA-FR 10 122622403 122622403 single base substitution T C exon_variant LICA-FR 10 122622403 122622403 single base substitution T C intron_variant LICA-FR 10 122622403 122622403 single base substitution T C missense_variant V228A 683T>C LICA-FR 10 122624171 122624171 single base substitution T A downstream_gene_variant LICA-FR 10 122624171 122624171 single base substitution T A intron_variant LICA-FR 10 122624171 122624171 single base substitution T A upstream_gene_variant LICA-FR 10 122624681 122624681 single base substitution T C downstream_gene_variant LICA-FR 10 122624681 122624681 single base substitution T C exon_variant LICA-FR 10 122624681 122624681 single base substitution T C intron_variant LICA-FR 10 122624681 122624681 single base substitution T C missense_variant V20A 59T>C LICA-FR 10 122624681 122624681 single base substitution T C missense_variant V279A 836T>C LICA-FR 10 122624681 122624681 single base substitution T C upstream_gene_variant LICA-FR 10 122627464 122627464 single base substitution G T downstream_gene_variant LICA-FR 10 122627464 122627464 single base substitution G T intron_variant LICA-FR 10 122627464 122627464 single base substitution G T upstream_gene_variant LICA-FR 10 122629979 122629979 single base substitution G T intron_variant LICA-FR 10 122635191 122635191 single base substitution A G intron_variant LICA-FR 10 122635191 122635191 single base substitution A G upstream_gene_variant LICA-FR 10 122638080 122638080 single base substitution C T intron_variant LICA-FR 10 122638080 122638080 single base substitution C T upstream_gene_variant LICA-FR 10 122639064 122639064 single base substitution G T exon_variant LICA-FR 10 122639064 122639064 single base substitution G T intron_variant LICA-FR 10 122640328 122640328 single base substitution G T intron_variant LICA-FR 10 122640328 122640328 single base substitution G T upstream_gene_variant LICA-FR 10 122652299 122652299 single base substitution G A downstream_gene_variant LICA-FR 10 122652299 122652299 single base substitution G A intron_variant LICA-FR 10 122664909 122664909 single base substitution G C 3_prime_UTR_variant LICA-FR 10 122664909 122664909 single base substitution G C downstream_gene_variant LICA-FR 10 122664909 122664909 single base substitution G C exon_variant LICA-FR 10 122664909 122664909 single base substitution G C missense_variant R1091P 3272G>C LICA-FR 10 122664909 122664909 single base substitution G C upstream_gene_variant LICA-FR 10 122666454 122666454 single base substitution A T downstream_gene_variant LICA-FR 10 122666454 122666454 single base substitution A T intron_variant LICA-FR 10 122666454 122666454 single base substitution A T upstream_gene_variant LICA-FR 10 122667321 122667321 insertion of <=200bp - T downstream_gene_variant LICA-FR 10 122667321 122667321 insertion of <=200bp - T exon_variant LICA-FR 10 122667321 122667321 insertion of <=200bp - T intron_variant LICA-FR 10 122671023 122671023 single base substitution C G downstream_gene_variant LICA-FR 10 122671210 122671210 single base substitution C A downstream_gene_variant LICA-FR 10 122671250 122671250 single base substitution T C downstream_gene_variant LICA-FR 10 122672357 122672357 single base substitution A G downstream_gene_variant LICA-FR 10 122672367 122672367 single base substitution A G downstream_gene_variant LICA-FR 10 122672947 122672947 single base substitution C T downstream_gene_variant LINC-JP 10 122610938 122610938 single base substitution G A exon_variant LINC-JP 10 122610938 122610938 single base substitution G A synonymous_variant L2L 6G>A LINC-JP 10 122610938 122610938 single base substitution G A upstream_gene_variant LINC-JP 10 122612190 122612190 single base substitution A G intron_variant LINC-JP 10 122612192 122612192 single base substitution A G intron_variant LINC-JP 10 122612716 122612716 single base substitution A G intron_variant LINC-JP 10 122614228 122614228 single base substitution G T intron_variant LINC-JP 10 122616506 122616506 single base substitution T C intron_variant LINC-JP 10 122621326 122621326 single base substitution G A downstream_gene_variant LINC-JP 10 122621326 122621326 single base substitution G A intron_variant LINC-JP 10 122621326 122621326 single base substitution G A upstream_gene_variant LINC-JP 10 122625127 122625127 single base substitution A G downstream_gene_variant LINC-JP 10 122625127 122625127 single base substitution A G intron_variant LINC-JP 10 122625127 122625127 single base substitution A G upstream_gene_variant LINC-JP 10 122626570 122626570 single base substitution C A downstream_gene_variant LINC-JP 10 122626570 122626570 single base substitution C A intron_variant LINC-JP 10 122626570 122626570 single base substitution C A splice_region_variant LINC-JP 10 122626570 122626570 single base substitution C A upstream_gene_variant LINC-JP 10 122630829 122630829 single base substitution T A exon_variant LINC-JP 10 122630829 122630829 single base substitution T A missense_variant I222N 665T>A LINC-JP 10 122630829 122630829 single base substitution T A missense_variant I481N 1442T>A LINC-JP 10 122631037 122631037 single base substitution C T intron_variant LINC-JP 10 122635490 122635490 single base substitution C T intron_variant LINC-JP 10 122635490 122635490 single base substitution C T upstream_gene_variant LINC-JP 10 122638201 122638201 single base substitution G A intron_variant LINC-JP 10 122638201 122638201 single base substitution G A upstream_gene_variant LINC-JP 10 122647457 122647457 single base substitution A T downstream_gene_variant LINC-JP 10 122647457 122647457 single base substitution A T intron_variant LINC-JP 10 122649724 122649724 single base substitution A T downstream_gene_variant LINC-JP 10 122649724 122649724 single base substitution A T intron_variant LINC-JP 10 122660506 122660506 single base substitution A T intron_variant LINC-JP 10 122660506 122660506 single base substitution A T upstream_gene_variant LINC-JP 10 122662515 122662515 single base substitution A G intron_variant LINC-JP 10 122662515 122662515 single base substitution A G upstream_gene_variant LINC-JP 10 122666929 122666929 single base substitution T C downstream_gene_variant LINC-JP 10 122666929 122666929 single base substitution T C exon_variant LINC-JP 10 122666929 122666929 single base substitution T C intron_variant LIRI-JP 10 122608261 122608261 single base substitution T C upstream_gene_variant LIRI-JP 10 122610695 122610695 single base substitution C G 5_prime_UTR_variant LIRI-JP 10 122610695 122610695 single base substitution C G upstream_gene_variant LIRI-JP 10 122610727 122610733 deletion of <=200bp ACCTAGG - 5_prime_UTR_variant LIRI-JP 10 122610727 122610733 deletion of <=200bp ACCTAGG - upstream_gene_variant LIRI-JP 10 122610847 122610847 single base substitution C A 5_prime_UTR_variant LIRI-JP 10 122610847 122610847 single base substitution C A exon_variant LIRI-JP 10 122610847 122610847 single base substitution C A upstream_gene_variant LIRI-JP 10 122613305 122613305 single base substitution G T intron_variant LIRI-JP 10 122613669 122613669 single base substitution A G intron_variant LIRI-JP 10 122613985 122613985 single base substitution C G intron_variant LIRI-JP 10 122616992 122616992 single base substitution C G intron_variant LIRI-JP 10 122616992 122616992 single base substitution C G upstream_gene_variant LIRI-JP 10 122618168 122618168 single base substitution G A 5_prime_UTR_variant LIRI-JP 10 122618168 122618168 single base substitution G A exon_variant LIRI-JP 10 122618168 122618168 single base substitution G A intron_variant LIRI-JP 10 122618168 122618168 single base substitution G A missense_variant R71K 212G>A LIRI-JP 10 122618168 122618168 single base substitution G A upstream_gene_variant LIRI-JP 10 122622021 122622021 single base substitution A G downstream_gene_variant LIRI-JP 10 122622021 122622021 single base substitution A G exon_variant LIRI-JP 10 122622021 122622021 single base substitution A G intron_variant LIRI-JP 10 122623799 122623815 deletion of <=200bp TTTTAAATTTCAAAGCC - downstream_gene_variant LIRI-JP 10 122623799 122623815 deletion of <=200bp TTTTAAATTTCAAAGCC - intron_variant LIRI-JP 10 122623799 122623815 deletion of <=200bp TTTTAAATTTCAAAGCC - upstream_gene_variant LIRI-JP 10 122623967 122623967 insertion of <=200bp - A downstream_gene_variant LIRI-JP 10 122623967 122623967 insertion of <=200bp - A intron_variant LIRI-JP 10 122623967 122623967 insertion of <=200bp - A upstream_gene_variant LIRI-JP 10 122624642 122624642 single base substitution G C downstream_gene_variant LIRI-JP 10 122624642 122624642 single base substitution G C exon_variant LIRI-JP 10 122624642 122624642 single base substitution G C intron_variant LIRI-JP 10 122624642 122624642 single base substitution G C missense_variant R266P 797G>C LIRI-JP 10 122624642 122624642 single base substitution G C missense_variant R7P 20G>C LIRI-JP 10 122624642 122624642 single base substitution G C upstream_gene_variant LIRI-JP 10 122630574 122630574 single base substitution A G intron_variant LIRI-JP 10 122635844 122635844 single base substitution A G intron_variant LIRI-JP 10 122635844 122635844 single base substitution A G upstream_gene_variant LIRI-JP 10 122636584 122636584 single base substitution A G intron_variant LIRI-JP 10 122636584 122636584 single base substitution A G upstream_gene_variant LIRI-JP 10 122637942 122637942 single base substitution A G 3_prime_UTR_variant LIRI-JP 10 122637942 122637942 single base substitution A G exon_variant LIRI-JP 10 122637942 122637942 single base substitution A G missense_variant N286S 857A>G LIRI-JP 10 122637942 122637942 single base substitution A G missense_variant N545S 1634A>G LIRI-JP 10 122637942 122637942 single base substitution A G upstream_gene_variant LIRI-JP 10 122638040 122638040 single base substitution T C intron_variant LIRI-JP 10 122638040 122638040 single base substitution T C upstream_gene_variant LIRI-JP 10 122638372 122638372 single base substitution T C intron_variant LIRI-JP 10 122638372 122638372 single base substitution T C upstream_gene_variant LIRI-JP 10 122639280 122639288 deletion of <=200bp ATGATGGAA - exon_variant LIRI-JP 10 122639280 122639288 deletion of <=200bp ATGATGGAA - intron_variant LIRI-JP 10 122640155 122640155 single base substitution A G intron_variant LIRI-JP 10 122640155 122640155 single base substitution A G upstream_gene_variant LIRI-JP 10 122641561 122641561 single base substitution A G downstream_gene_variant LIRI-JP 10 122641561 122641561 single base substitution A G intron_variant LIRI-JP 10 122641561 122641561 single base substitution A G upstream_gene_variant LIRI-JP 10 122641902 122641902 single base substitution C A downstream_gene_variant LIRI-JP 10 122641902 122641902 single base substitution C A intron_variant LIRI-JP 10 122641902 122641902 single base substitution C A upstream_gene_variant LIRI-JP 10 122642374 122642374 single base substitution A G downstream_gene_variant LIRI-JP 10 122642374 122642374 single base substitution A G intron_variant LIRI-JP 10 122642374 122642374 single base substitution A G upstream_gene_variant LIRI-JP 10 122642863 122642863 single base substitution G T downstream_gene_variant LIRI-JP 10 122642863 122642863 single base substitution G T intron_variant LIRI-JP 10 122642863 122642863 single base substitution G T upstream_gene_variant LIRI-JP 10 122644057 122644057 single base substitution A T downstream_gene_variant LIRI-JP 10 122644057 122644057 single base substitution A T intron_variant LIRI-JP 10 122644057 122644057 single base substitution A T upstream_gene_variant LIRI-JP 10 122645051 122645051 single base substitution G A downstream_gene_variant LIRI-JP 10 122645051 122645051 single base substitution G A intron_variant LIRI-JP 10 122645051 122645051 single base substitution G A upstream_gene_variant LIRI-JP 10 122645548 122645548 single base substitution G T downstream_gene_variant LIRI-JP 10 122645548 122645548 single base substitution G T intron_variant LIRI-JP 10 122646185 122646185 single base substitution T C downstream_gene_variant LIRI-JP 10 122646185 122646185 single base substitution T C intron_variant LIRI-JP 10 122646700 122646700 single base substitution A C downstream_gene_variant LIRI-JP 10 122646700 122646700 single base substitution A C intron_variant LIRI-JP 10 122647084 122647084 single base substitution A C downstream_gene_variant LIRI-JP 10 122647084 122647084 single base substitution A C intron_variant LIRI-JP 10 122647267 122647267 single base substitution T C downstream_gene_variant LIRI-JP 10 122647267 122647267 single base substitution T C intron_variant LIRI-JP 10 122651868 122651868 single base substitution A G downstream_gene_variant LIRI-JP 10 122651868 122651868 single base substitution A G intron_variant LIRI-JP 10 122651998 122651998 single base substitution A G downstream_gene_variant LIRI-JP 10 122651998 122651998 single base substitution A G intron_variant LIRI-JP 10 122652172 122652172 deletion of <=200bp T - downstream_gene_variant LIRI-JP 10 122652172 122652172 deletion of <=200bp T - intron_variant LIRI-JP 10 122654507 122654507 single base substitution T C intron_variant LIRI-JP 10 122654507 122654507 single base substitution T C upstream_gene_variant LIRI-JP 10 122654513 122654518 deletion of <=200bp AATAAC - intron_variant LIRI-JP 10 122654513 122654518 deletion of <=200bp AATAAC - upstream_gene_variant LIRI-JP 10 122656955 122656955 single base substitution G T intron_variant LIRI-JP 10 122656955 122656955 single base substitution G T upstream_gene_variant LIRI-JP 10 122657450 122657450 single base substitution A T intron_variant LIRI-JP 10 122657450 122657450 single base substitution A T upstream_gene_variant LIRI-JP 10 122658275 122658275 single base substitution C T intron_variant LIRI-JP 10 122658275 122658275 single base substitution C T upstream_gene_variant LIRI-JP 10 122660363 122660363 single base substitution A C intron_variant LIRI-JP 10 122660363 122660363 single base substitution A C upstream_gene_variant LIRI-JP 10 122660459 122660459 single base substitution C G intron_variant LIRI-JP 10 122660459 122660459 single base substitution C G upstream_gene_variant LIRI-JP 10 122662889 122662889 single base substitution G A downstream_gene_variant LIRI-JP 10 122662889 122662889 single base substitution G A intron_variant LIRI-JP 10 122662889 122662889 single base substitution G A upstream_gene_variant LIRI-JP 10 122663149 122663149 single base substitution T C downstream_gene_variant LIRI-JP 10 122663149 122663149 single base substitution T C intron_variant LIRI-JP 10 122663149 122663149 single base substitution T C upstream_gene_variant LIRI-JP 10 122663512 122663512 single base substitution A G downstream_gene_variant LIRI-JP 10 122663512 122663512 single base substitution A G intron_variant LIRI-JP 10 122663512 122663512 single base substitution A G upstream_gene_variant LIRI-JP 10 122663887 122663887 single base substitution A G downstream_gene_variant LIRI-JP 10 122663887 122663887 single base substitution A G intron_variant LIRI-JP 10 122663887 122663887 single base substitution A G upstream_gene_variant LIRI-JP 10 122665583 122665583 single base substitution C T 3_prime_UTR_variant LIRI-JP 10 122665583 122665583 single base substitution C T downstream_gene_variant LIRI-JP 10 122665583 122665583 single base substitution C T intron_variant LIRI-JP 10 122665583 122665583 single base substitution C T upstream_gene_variant LIRI-JP 10 122669273 122669273 single base substitution G C downstream_gene_variant LUSC-KR 10 122605733 122605733 single base substitution T C upstream_gene_variant LUSC-KR 10 122605746 122605746 single base substitution A G upstream_gene_variant LUSC-KR 10 122605979 122605979 single base substitution C G upstream_gene_variant LUSC-KR 10 122607716 122607716 single base substitution A G upstream_gene_variant LUSC-KR 10 122607833 122607833 single base substitution C T upstream_gene_variant LUSC-KR 10 122607857 122607857 single base substitution C A upstream_gene_variant LUSC-KR 10 122607899 122607899 single base substitution T C upstream_gene_variant LUSC-KR 10 122607901 122607901 single base substitution C T upstream_gene_variant LUSC-KR 10 122607921 122607921 single base substitution C G upstream_gene_variant LUSC-KR 10 122607932 122607932 single base substitution G A upstream_gene_variant LUSC-KR 10 122607996 122607996 single base substitution C T upstream_gene_variant LUSC-KR 10 122608004 122608004 single base substitution G A upstream_gene_variant LUSC-KR 10 122608023 122608023 single base substitution C A upstream_gene_variant LUSC-KR 10 122608049 122608049 single base substitution C G upstream_gene_variant LUSC-KR 10 122614372 122614372 single base substitution G C intron_variant LUSC-KR 10 122623627 122623627 single base substitution C A downstream_gene_variant LUSC-KR 10 122623627 122623627 single base substitution C A intron_variant LUSC-KR 10 122623627 122623627 single base substitution C A upstream_gene_variant LUSC-KR 10 122623964 122623964 single base substitution A G downstream_gene_variant LUSC-KR 10 122623964 122623964 single base substitution A G intron_variant LUSC-KR 10 122623964 122623964 single base substitution A G upstream_gene_variant LUSC-KR 10 122628624 122628624 single base substitution T G downstream_gene_variant LUSC-KR 10 122628624 122628624 single base substitution T G intron_variant LUSC-KR 10 122628641 122628641 single base substitution G T downstream_gene_variant LUSC-KR 10 122628641 122628641 single base substitution G T intron_variant LUSC-KR 10 122660701 122660701 single base substitution C T intron_variant LUSC-KR 10 122660701 122660701 single base substitution C T upstream_gene_variant LUSC-KR 10 122662483 122662483 single base substitution C T intron_variant LUSC-KR 10 122662483 122662483 single base substitution C T upstream_gene_variant LUSC-KR 10 122662533 122662533 single base substitution G C intron_variant LUSC-KR 10 122662533 122662533 single base substitution G C upstream_gene_variant LUSC-KR 10 122666712 122666712 single base substitution C G downstream_gene_variant LUSC-KR 10 122666712 122666712 single base substitution C G intron_variant LUSC-KR 10 122666712 122666712 single base substitution C G upstream_gene_variant LUSC-KR 10 122668791 122668791 single base substitution G T 3_prime_UTR_variant LUSC-KR 10 122668791 122668791 single base substitution G T downstream_gene_variant LUSC-KR 10 122668791 122668791 single base substitution G T exon_variant LUSC-KR 10 122669996 122669996 single base substitution G T downstream_gene_variant LUSC-KR 10 122670868 122670868 single base substitution A T downstream_gene_variant LUSC-KR 10 122671476 122671476 single base substitution G C downstream_gene_variant LUSC-KR 10 122671481 122671481 single base substitution C A downstream_gene_variant LUSC-KR 10 122671482 122671482 single base substitution G A downstream_gene_variant LUSC-KR 10 122672776 122672776 single base substitution G C downstream_gene_variant LUSC-KR 10 122672860 122672860 single base substitution A C downstream_gene_variant LUSC-KR 10 122672947 122672947 single base substitution C T downstream_gene_variant LUSC-KR 10 122672976 122672976 single base substitution T C downstream_gene_variant LUSC-KR 10 122673017 122673017 single base substitution A G downstream_gene_variant LUSC-KR 10 122673199 122673199 single base substitution A G downstream_gene_variant LUSC-KR 10 122673615 122673615 single base substitution A G downstream_gene_variant LUSC-KR 10 122673623 122673623 single base substitution G C downstream_gene_variant LUSC-KR 10 122673654 122673654 single base substitution C T downstream_gene_variant LUSC-KR 10 122674010 122674010 single base substitution T C downstream_gene_variant LUSC-KR 10 122674012 122674012 single base substitution G A downstream_gene_variant LUSC-US 10 122618251 122618251 single base substitution G C 5_prime_UTR_variant LUSC-US 10 122618251 122618251 single base substitution G C exon_variant LUSC-US 10 122618251 122618251 single base substitution G C intron_variant LUSC-US 10 122618251 122618251 single base substitution G C missense_variant D99H 295G>C LUSC-US 10 122618251 122618251 single base substitution G C upstream_gene_variant LUSC-US 10 122659586 122659586 single base substitution C A 3_prime_UTR_variant LUSC-US 10 122659586 122659586 single base substitution C A exon_variant LUSC-US 10 122659586 122659586 single base substitution C A missense_variant A854D 2561C>A LUSC-US 10 122659586 122659586 single base substitution C A upstream_gene_variant LUSC-US 10 122664830 122664830 single base substitution G A downstream_gene_variant LUSC-US 10 122664830 122664830 single base substitution G A intron_variant LUSC-US 10 122664830 122664830 single base substitution G A splice_acceptor_variant LUSC-US 10 122664830 122664830 single base substitution G A upstream_gene_variant LUSC-US 10 122666322 122666322 single base substitution G A 3_prime_UTR_variant LUSC-US 10 122666322 122666322 single base substitution G A downstream_gene_variant LUSC-US 10 122666322 122666322 single base substitution G A exon_variant LUSC-US 10 122666322 122666322 single base substitution G A missense_variant E1158K 3472G>A LUSC-US 10 122666322 122666322 single base substitution G A upstream_gene_variant LUSC-US 10 122666349 122666349 single base substitution G T 3_prime_UTR_variant LUSC-US 10 122666349 122666349 single base substitution G T downstream_gene_variant LUSC-US 10 122666349 122666349 single base substitution G T exon_variant LUSC-US 10 122666349 122666349 single base substitution G T stop_gained E1167* 3499G>T LUSC-US 10 122666349 122666349 single base substitution G T upstream_gene_variant MALY-DE 10 122612041 122612041 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant MALY-DE 10 122612041 122612041 single base substitution G T exon_variant MALY-DE 10 122612041 122612041 single base substitution G T intron_variant MALY-DE 10 122612041 122612041 single base substitution G T missense_variant W31L 92G>T MALY-DE 10 122612041 122612041 single base substitution G T upstream_gene_variant MALY-DE 10 122612857 122612857 single base substitution A T intron_variant MALY-DE 10 122617609 122617609 single base substitution A T intron_variant MALY-DE 10 122617609 122617609 single base substitution A T upstream_gene_variant MALY-DE 10 122624604 122624604 single base substitution G A 5_prime_UTR_variant MALY-DE 10 122624604 122624604 single base substitution G A downstream_gene_variant MALY-DE 10 122624604 122624604 single base substitution G A exon_variant MALY-DE 10 122624604 122624604 single base substitution G A intron_variant MALY-DE 10 122624604 122624604 single base substitution G A synonymous_variant L253L 759G>A MALY-DE 10 122624604 122624604 single base substitution G A upstream_gene_variant MALY-DE 10 122629266 122629266 single base substitution G A downstream_gene_variant MALY-DE 10 122629266 122629266 single base substitution G A intron_variant MALY-DE 10 122631575 122631575 single base substitution A G intron_variant MALY-DE 10 122645567 122645567 single base substitution A G downstream_gene_variant MALY-DE 10 122645567 122645567 single base substitution A G intron_variant MALY-DE 10 122659295 122659295 insertion of <=200bp - A intron_variant MALY-DE 10 122659295 122659295 insertion of <=200bp - A upstream_gene_variant MELA-AU 10 122605987 122605987 single base substitution C T upstream_gene_variant MELA-AU 10 122606519 122606519 single base substitution C T upstream_gene_variant MELA-AU 10 122607524 122607524 single base substitution C T upstream_gene_variant MELA-AU 10 122608730 122608730 insertion of <=200bp - C upstream_gene_variant MELA-AU 10 122608858 122608858 single base substitution G A upstream_gene_variant MELA-AU 10 122609012 122609012 single base substitution G A upstream_gene_variant MELA-AU 10 122609378 122609378 single base substitution C T upstream_gene_variant MELA-AU 10 122609448 122609448 single base substitution C T upstream_gene_variant MELA-AU 10 122609536 122609536 single base substitution G A upstream_gene_variant MELA-AU 10 122609920 122609920 single base substitution C T upstream_gene_variant MELA-AU 10 122610756 122610756 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 10 122610756 122610756 single base substitution G T upstream_gene_variant MELA-AU 10 122610930 122610930 single base substitution G A 5_prime_UTR_variant MELA-AU 10 122610930 122610930 single base substitution G A exon_variant MELA-AU 10 122610930 122610930 single base substitution G A upstream_gene_variant MELA-AU 10 122611908 122611908 single base substitution C A exon_variant MELA-AU 10 122611908 122611908 single base substitution C A intron_variant MELA-AU 10 122611908 122611908 single base substitution C A upstream_gene_variant MELA-AU 10 122612093 122612093 single base substitution C T 5_prime_UTR_variant MELA-AU 10 122612093 122612093 single base substitution C T exon_variant MELA-AU 10 122612093 122612093 single base substitution C T intron_variant MELA-AU 10 122612093 122612093 single base substitution C T synonymous_variant S48S 144C>T MELA-AU 10 122612093 122612093 single base substitution C T upstream_gene_variant MELA-AU 10 122612888 122612888 single base substitution C T intron_variant MELA-AU 10 122612967 122612967 single base substitution C T intron_variant MELA-AU 10 122613245 122613245 single base substitution C T intron_variant MELA-AU 10 122613512 122613512 single base substitution G A intron_variant MELA-AU 10 122613525 122613525 single base substitution T C intron_variant MELA-AU 10 122613577 122613577 single base substitution G A intron_variant MELA-AU 10 122613681 122613681 single base substitution A G intron_variant MELA-AU 10 122614016 122614016 single base substitution C T intron_variant MELA-AU 10 122614526 122614526 single base substitution C A intron_variant MELA-AU 10 122614875 122614875 single base substitution T A intron_variant MELA-AU 10 122615547 122615548 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 122615738 122615738 single base substitution C T intron_variant MELA-AU 10 122615853 122615853 single base substitution G A intron_variant MELA-AU 10 122616958 122616958 single base substitution T C intron_variant MELA-AU 10 122617102 122617102 single base substitution C T intron_variant MELA-AU 10 122617102 122617102 single base substitution C T upstream_gene_variant MELA-AU 10 122619014 122619014 single base substitution C T downstream_gene_variant MELA-AU 10 122619014 122619014 single base substitution C T intron_variant MELA-AU 10 122619014 122619014 single base substitution C T upstream_gene_variant MELA-AU 10 122619296 122619296 single base substitution T C downstream_gene_variant MELA-AU 10 122619296 122619296 single base substitution T C intron_variant MELA-AU 10 122619296 122619296 single base substitution T C upstream_gene_variant MELA-AU 10 122619678 122619678 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 10 122619678 122619678 single base substitution C T downstream_gene_variant MELA-AU 10 122619678 122619678 single base substitution C T exon_variant MELA-AU 10 122619678 122619678 single base substitution C T intron_variant MELA-AU 10 122619678 122619678 single base substitution C T missense_variant P137L 410C>T MELA-AU 10 122619678 122619678 single base substitution C T upstream_gene_variant MELA-AU 10 122619975 122619975 single base substitution C T downstream_gene_variant MELA-AU 10 122619975 122619975 single base substitution C T intron_variant MELA-AU 10 122619975 122619975 single base substitution C T upstream_gene_variant MELA-AU 10 122620002 122620002 single base substitution T C downstream_gene_variant MELA-AU 10 122620002 122620002 single base substitution T C intron_variant MELA-AU 10 122620002 122620002 single base substitution T C upstream_gene_variant MELA-AU 10 122620623 122620623 single base substitution C G downstream_gene_variant MELA-AU 10 122620623 122620623 single base substitution C G intron_variant MELA-AU 10 122620623 122620623 single base substitution C G upstream_gene_variant MELA-AU 10 122620693 122620693 single base substitution G T downstream_gene_variant MELA-AU 10 122620693 122620693 single base substitution G T intron_variant MELA-AU 10 122620693 122620693 single base substitution G T upstream_gene_variant MELA-AU 10 122621664 122621664 single base substitution T G downstream_gene_variant MELA-AU 10 122621664 122621664 single base substitution T G intron_variant MELA-AU 10 122621664 122621664 single base substitution T G upstream_gene_variant MELA-AU 10 122621693 122621695 multiple base substitution (>=2bp and <=200bp) CCC TTA downstream_gene_variant MELA-AU 10 122621693 122621695 multiple base substitution (>=2bp and <=200bp) CCC TTA intron_variant MELA-AU 10 122621693 122621695 multiple base substitution (>=2bp and <=200bp) CCC TTA upstream_gene_variant MELA-AU 10 122622301 122622301 single base substitution C T 5_prime_UTR_variant MELA-AU 10 122622301 122622301 single base substitution C T downstream_gene_variant MELA-AU 10 122622301 122622301 single base substitution C T exon_variant MELA-AU 10 122622301 122622301 single base substitution C T intron_variant MELA-AU 10 122622301 122622301 single base substitution C T missense_variant P194L 581C>T MELA-AU 10 122622724 122622724 single base substitution C T downstream_gene_variant MELA-AU 10 122622724 122622724 single base substitution C T intron_variant MELA-AU 10 122623072 122623072 single base substitution T C downstream_gene_variant MELA-AU 10 122623072 122623072 single base substitution T C intron_variant MELA-AU 10 122623821 122623821 single base substitution A T downstream_gene_variant MELA-AU 10 122623821 122623821 single base substitution A T intron_variant MELA-AU 10 122623821 122623821 single base substitution A T upstream_gene_variant MELA-AU 10 122623827 122623827 deletion of <=200bp T - downstream_gene_variant MELA-AU 10 122623827 122623827 deletion of <=200bp T - intron_variant MELA-AU 10 122623827 122623827 deletion of <=200bp T - upstream_gene_variant MELA-AU 10 122623981 122623981 single base substitution C T downstream_gene_variant MELA-AU 10 122623981 122623981 single base substitution C T intron_variant MELA-AU 10 122623981 122623981 single base substitution C T upstream_gene_variant MELA-AU 10 122624174 122624174 single base substitution C T downstream_gene_variant MELA-AU 10 122624174 122624174 single base substitution C T intron_variant MELA-AU 10 122624174 122624174 single base substitution C T upstream_gene_variant MELA-AU 10 122624950 122624950 single base substitution A G downstream_gene_variant MELA-AU 10 122624950 122624950 single base substitution A G intron_variant MELA-AU 10 122624950 122624950 single base substitution A G upstream_gene_variant MELA-AU 10 122625051 122625051 single base substitution C T downstream_gene_variant MELA-AU 10 122625051 122625051 single base substitution C T intron_variant MELA-AU 10 122625051 122625051 single base substitution C T upstream_gene_variant MELA-AU 10 122625551 122625551 single base substitution C T downstream_gene_variant MELA-AU 10 122625551 122625551 single base substitution C T intron_variant MELA-AU 10 122625551 122625551 single base substitution C T upstream_gene_variant MELA-AU 10 122625901 122625901 single base substitution C T downstream_gene_variant MELA-AU 10 122625901 122625901 single base substitution C T intron_variant MELA-AU 10 122625901 122625901 single base substitution C T upstream_gene_variant MELA-AU 10 122626158 122626158 single base substitution C T downstream_gene_variant MELA-AU 10 122626158 122626158 single base substitution C T exon_variant MELA-AU 10 122626158 122626158 single base substitution C T intron_variant MELA-AU 10 122626158 122626158 single base substitution C T missense_variant P358S 1072C>T MELA-AU 10 122626158 122626158 single base substitution C T missense_variant P99S 295C>T MELA-AU 10 122626158 122626158 single base substitution C T upstream_gene_variant MELA-AU 10 122627068 122627068 single base substitution C T downstream_gene_variant MELA-AU 10 122627068 122627068 single base substitution C T intron_variant MELA-AU 10 122627068 122627068 single base substitution C T upstream_gene_variant MELA-AU 10 122627144 122627144 single base substitution C T downstream_gene_variant MELA-AU 10 122627144 122627144 single base substitution C T intron_variant MELA-AU 10 122627144 122627144 single base substitution C T upstream_gene_variant MELA-AU 10 122627365 122627365 single base substitution A T downstream_gene_variant MELA-AU 10 122627365 122627365 single base substitution A T intron_variant MELA-AU 10 122627365 122627365 single base substitution A T upstream_gene_variant MELA-AU 10 122627838 122627838 single base substitution T G downstream_gene_variant MELA-AU 10 122627838 122627838 single base substitution T G intron_variant MELA-AU 10 122627838 122627838 single base substitution T G upstream_gene_variant MELA-AU 10 122628204 122628204 single base substitution G A downstream_gene_variant MELA-AU 10 122628204 122628204 single base substitution G A exon_variant MELA-AU 10 122628204 122628204 single base substitution G A intron_variant MELA-AU 10 122629796 122629796 single base substitution C T intron_variant MELA-AU 10 122629953 122629953 single base substitution C T intron_variant MELA-AU 10 122630478 122630478 single base substitution C T intron_variant MELA-AU 10 122632077 122632077 single base substitution A T intron_variant MELA-AU 10 122632507 122632507 single base substitution C T intron_variant MELA-AU 10 122633008 122633008 single base substitution C T intron_variant MELA-AU 10 122633915 122633915 single base substitution T A intron_variant MELA-AU 10 122633915 122633915 single base substitution T A upstream_gene_variant MELA-AU 10 122634253 122634254 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 122634253 122634254 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 122634588 122634588 deletion of <=200bp T - intron_variant MELA-AU 10 122634588 122634588 deletion of <=200bp T - upstream_gene_variant MELA-AU 10 122634670 122634670 single base substitution T A intron_variant MELA-AU 10 122634670 122634670 single base substitution T A upstream_gene_variant MELA-AU 10 122634736 122634736 single base substitution G A intron_variant MELA-AU 10 122634736 122634736 single base substitution G A upstream_gene_variant MELA-AU 10 122634785 122634785 single base substitution C T intron_variant MELA-AU 10 122634785 122634785 single base substitution C T upstream_gene_variant MELA-AU 10 122635311 122635311 single base substitution C T intron_variant MELA-AU 10 122635311 122635311 single base substitution C T upstream_gene_variant MELA-AU 10 122635800 122635800 single base substitution C T intron_variant MELA-AU 10 122635800 122635800 single base substitution C T upstream_gene_variant MELA-AU 10 122635806 122635806 single base substitution A G intron_variant MELA-AU 10 122635806 122635806 single base substitution A G upstream_gene_variant MELA-AU 10 122636813 122636813 single base substitution C T intron_variant MELA-AU 10 122636813 122636813 single base substitution C T upstream_gene_variant MELA-AU 10 122636966 122636966 single base substitution C T intron_variant MELA-AU 10 122636966 122636966 single base substitution C T upstream_gene_variant MELA-AU 10 122637328 122637328 single base substitution C T intron_variant MELA-AU 10 122637328 122637328 single base substitution C T upstream_gene_variant MELA-AU 10 122638062 122638062 single base substitution G A intron_variant MELA-AU 10 122638062 122638062 single base substitution G A upstream_gene_variant MELA-AU 10 122639031 122639031 single base substitution C T exon_variant MELA-AU 10 122639031 122639031 single base substitution C T intron_variant MELA-AU 10 122639445 122639445 single base substitution C T exon_variant MELA-AU 10 122639445 122639445 single base substitution C T intron_variant MELA-AU 10 122639755 122639755 single base substitution C T exon_variant MELA-AU 10 122639755 122639755 single base substitution C T intron_variant MELA-AU 10 122639755 122639755 single base substitution C T upstream_gene_variant MELA-AU 10 122641613 122641613 single base substitution C T downstream_gene_variant MELA-AU 10 122641613 122641613 single base substitution C T intron_variant MELA-AU 10 122641613 122641613 single base substitution C T upstream_gene_variant MELA-AU 10 122642190 122642190 single base substitution C T downstream_gene_variant MELA-AU 10 122642190 122642190 single base substitution C T intron_variant MELA-AU 10 122642190 122642190 single base substitution C T upstream_gene_variant MELA-AU 10 122642386 122642386 single base substitution T A downstream_gene_variant MELA-AU 10 122642386 122642386 single base substitution T A intron_variant MELA-AU 10 122642386 122642386 single base substitution T A upstream_gene_variant MELA-AU 10 122642634 122642634 single base substitution C T downstream_gene_variant MELA-AU 10 122642634 122642634 single base substitution C T intron_variant MELA-AU 10 122642634 122642634 single base substitution C T upstream_gene_variant MELA-AU 10 122643583 122643583 single base substitution A T downstream_gene_variant MELA-AU 10 122643583 122643583 single base substitution A T intron_variant MELA-AU 10 122643583 122643583 single base substitution A T upstream_gene_variant MELA-AU 10 122643695 122643695 single base substitution C T downstream_gene_variant MELA-AU 10 122643695 122643695 single base substitution C T intron_variant MELA-AU 10 122643695 122643695 single base substitution C T upstream_gene_variant MELA-AU 10 122644147 122644147 single base substitution T A downstream_gene_variant MELA-AU 10 122644147 122644147 single base substitution T A intron_variant MELA-AU 10 122644147 122644147 single base substitution T A upstream_gene_variant MELA-AU 10 122644590 122644590 single base substitution C A downstream_gene_variant MELA-AU 10 122644590 122644590 single base substitution C A exon_variant MELA-AU 10 122644590 122644590 single base substitution C A intron_variant MELA-AU 10 122644590 122644590 single base substitution C A upstream_gene_variant MELA-AU 10 122645013 122645013 single base substitution C T downstream_gene_variant MELA-AU 10 122645013 122645013 single base substitution C T intron_variant MELA-AU 10 122645013 122645013 single base substitution C T upstream_gene_variant MELA-AU 10 122645161 122645161 single base substitution C T downstream_gene_variant MELA-AU 10 122645161 122645161 single base substitution C T intron_variant MELA-AU 10 122645161 122645161 single base substitution C T upstream_gene_variant MELA-AU 10 122645907 122645907 single base substitution C T downstream_gene_variant MELA-AU 10 122645907 122645907 single base substitution C T intron_variant MELA-AU 10 122646028 122646028 single base substitution G A downstream_gene_variant MELA-AU 10 122646028 122646028 single base substitution G A intron_variant MELA-AU 10 122646150 122646150 single base substitution C T downstream_gene_variant MELA-AU 10 122646150 122646150 single base substitution C T intron_variant MELA-AU 10 122647151 122647151 single base substitution C T downstream_gene_variant MELA-AU 10 122647151 122647151 single base substitution C T intron_variant MELA-AU 10 122647250 122647251 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 122647250 122647251 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 122647449 122647449 single base substitution T G downstream_gene_variant MELA-AU 10 122647449 122647449 single base substitution T G intron_variant MELA-AU 10 122647592 122647592 single base substitution C T downstream_gene_variant MELA-AU 10 122647592 122647592 single base substitution C T intron_variant MELA-AU 10 122648148 122648148 single base substitution C T downstream_gene_variant MELA-AU 10 122648148 122648148 single base substitution C T intron_variant MELA-AU 10 122648305 122648305 single base substitution C T downstream_gene_variant MELA-AU 10 122648305 122648305 single base substitution C T intron_variant MELA-AU 10 122648721 122648721 single base substitution T G exon_variant MELA-AU 10 122648721 122648721 single base substitution T G intron_variant MELA-AU 10 122649444 122649444 single base substitution C T 3_prime_UTR_variant MELA-AU 10 122649444 122649444 single base substitution C T exon_variant MELA-AU 10 122649444 122649444 single base substitution C T missense_variant R756C 2266C>T MELA-AU 10 122649528 122649528 single base substitution C T downstream_gene_variant MELA-AU 10 122649528 122649528 single base substitution C T splice_region_variant MELA-AU 10 122649640 122649640 single base substitution C T downstream_gene_variant MELA-AU 10 122649640 122649640 single base substitution C T intron_variant MELA-AU 10 122649790 122649790 single base substitution T C downstream_gene_variant MELA-AU 10 122649790 122649790 single base substitution T C intron_variant MELA-AU 10 122650469 122650469 single base substitution G A downstream_gene_variant MELA-AU 10 122650469 122650469 single base substitution G A intron_variant MELA-AU 10 122651123 122651123 single base substitution C T downstream_gene_variant MELA-AU 10 122651123 122651123 single base substitution C T intron_variant MELA-AU 10 122651761 122651761 single base substitution C T downstream_gene_variant MELA-AU 10 122651761 122651761 single base substitution C T intron_variant MELA-AU 10 122652464 122652464 single base substitution A T downstream_gene_variant MELA-AU 10 122652464 122652464 single base substitution A T intron_variant MELA-AU 10 122652728 122652728 single base substitution C T downstream_gene_variant MELA-AU 10 122652728 122652728 single base substitution C T intron_variant MELA-AU 10 122652733 122652733 single base substitution G A downstream_gene_variant MELA-AU 10 122652733 122652733 single base substitution G A intron_variant MELA-AU 10 122652943 122652943 single base substitution T G downstream_gene_variant MELA-AU 10 122652943 122652943 single base substitution T G intron_variant MELA-AU 10 122653800 122653800 single base substitution C T downstream_gene_variant MELA-AU 10 122653800 122653800 single base substitution C T intron_variant MELA-AU 10 122653880 122653880 single base substitution C T downstream_gene_variant MELA-AU 10 122653880 122653880 single base substitution C T intron_variant MELA-AU 10 122653974 122653974 single base substitution G A downstream_gene_variant MELA-AU 10 122653974 122653974 single base substitution G A intron_variant MELA-AU 10 122654362 122654362 single base substitution T A downstream_gene_variant MELA-AU 10 122654362 122654362 single base substitution T A intron_variant MELA-AU 10 122654362 122654362 single base substitution T A upstream_gene_variant MELA-AU 10 122655231 122655231 single base substitution C T intron_variant MELA-AU 10 122655231 122655231 single base substitution C T upstream_gene_variant MELA-AU 10 122655307 122655307 single base substitution T C intron_variant MELA-AU 10 122655307 122655307 single base substitution T C upstream_gene_variant MELA-AU 10 122656452 122656452 single base substitution C T intron_variant MELA-AU 10 122656452 122656452 single base substitution C T upstream_gene_variant MELA-AU 10 122656453 122656453 single base substitution C T intron_variant MELA-AU 10 122656453 122656453 single base substitution C T upstream_gene_variant MELA-AU 10 122656721 122656721 single base substitution G A intron_variant MELA-AU 10 122656721 122656721 single base substitution G A upstream_gene_variant MELA-AU 10 122656749 122656749 deletion of <=200bp G - intron_variant MELA-AU 10 122656749 122656749 deletion of <=200bp G - upstream_gene_variant MELA-AU 10 122656828 122656828 deletion of <=200bp A - intron_variant MELA-AU 10 122656828 122656828 deletion of <=200bp A - upstream_gene_variant MELA-AU 10 122656918 122656918 single base substitution C T intron_variant MELA-AU 10 122656918 122656918 single base substitution C T upstream_gene_variant MELA-AU 10 122657148 122657149 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 10 122657148 122657149 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 10 122657536 122657536 single base substitution C T intron_variant MELA-AU 10 122657536 122657536 single base substitution C T upstream_gene_variant MELA-AU 10 122657874 122657874 single base substitution C T intron_variant MELA-AU 10 122657874 122657874 single base substitution C T upstream_gene_variant MELA-AU 10 122657995 122657995 single base substitution C T intron_variant MELA-AU 10 122657995 122657995 single base substitution C T upstream_gene_variant MELA-AU 10 122658261 122658261 single base substitution C T intron_variant MELA-AU 10 122658261 122658261 single base substitution C T upstream_gene_variant MELA-AU 10 122658934 122658934 single base substitution C T intron_variant MELA-AU 10 122658934 122658934 single base substitution C T upstream_gene_variant MELA-AU 10 122660297 122660297 single base substitution C T intron_variant MELA-AU 10 122660297 122660297 single base substitution C T upstream_gene_variant MELA-AU 10 122661683 122661683 single base substitution C T intron_variant MELA-AU 10 122661683 122661683 single base substitution C T upstream_gene_variant MELA-AU 10 122663295 122663295 single base substitution C T downstream_gene_variant MELA-AU 10 122663295 122663295 single base substitution C T intron_variant MELA-AU 10 122663295 122663295 single base substitution C T upstream_gene_variant MELA-AU 10 122663466 122663466 single base substitution T C downstream_gene_variant MELA-AU 10 122663466 122663466 single base substitution T C intron_variant MELA-AU 10 122663466 122663466 single base substitution T C upstream_gene_variant MELA-AU 10 122663511 122663511 single base substitution C T downstream_gene_variant MELA-AU 10 122663511 122663511 single base substitution C T intron_variant MELA-AU 10 122663511 122663511 single base substitution C T upstream_gene_variant MELA-AU 10 122663547 122663547 single base substitution T A downstream_gene_variant MELA-AU 10 122663547 122663547 single base substitution T A intron_variant MELA-AU 10 122663547 122663547 single base substitution T A upstream_gene_variant MELA-AU 10 122663578 122663578 single base substitution T G 3_prime_UTR_variant MELA-AU 10 122663578 122663578 single base substitution T G downstream_gene_variant MELA-AU 10 122663578 122663578 single base substitution T G exon_variant MELA-AU 10 122663578 122663578 single base substitution T G missense_variant V984G 2951T>G MELA-AU 10 122663578 122663578 single base substitution T G upstream_gene_variant MELA-AU 10 122663790 122663790 single base substitution C T downstream_gene_variant MELA-AU 10 122663790 122663790 single base substitution C T intron_variant MELA-AU 10 122663790 122663790 single base substitution C T upstream_gene_variant MELA-AU 10 122664462 122664462 single base substitution C T downstream_gene_variant MELA-AU 10 122664462 122664462 single base substitution C T intron_variant MELA-AU 10 122664462 122664462 single base substitution C T upstream_gene_variant MELA-AU 10 122664765 122664765 single base substitution C T downstream_gene_variant MELA-AU 10 122664765 122664765 single base substitution C T intron_variant MELA-AU 10 122664765 122664765 single base substitution C T upstream_gene_variant MELA-AU 10 122665064 122665064 single base substitution C T downstream_gene_variant MELA-AU 10 122665064 122665064 single base substitution C T exon_variant MELA-AU 10 122665064 122665064 single base substitution C T intron_variant MELA-AU 10 122665064 122665064 single base substitution C T upstream_gene_variant MELA-AU 10 122665152 122665152 single base substitution C T downstream_gene_variant MELA-AU 10 122665152 122665152 single base substitution C T exon_variant MELA-AU 10 122665152 122665152 single base substitution C T intron_variant MELA-AU 10 122665152 122665152 single base substitution C T upstream_gene_variant MELA-AU 10 122665539 122665539 single base substitution C T 3_prime_UTR_variant MELA-AU 10 122665539 122665539 single base substitution C T downstream_gene_variant MELA-AU 10 122665539 122665539 single base substitution C T splice_region_variant MELA-AU 10 122665539 122665539 single base substitution C T upstream_gene_variant MELA-AU 10 122665539 122665540 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 10 122665539 122665540 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 122665539 122665540 multiple base substitution (>=2bp and <=200bp) CC TT splice_region_variant MELA-AU 10 122665539 122665540 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 122665894 122665894 single base substitution C T 3_prime_UTR_variant MELA-AU 10 122665894 122665894 single base substitution C T downstream_gene_variant MELA-AU 10 122665894 122665894 single base substitution C T intron_variant MELA-AU 10 122665894 122665894 single base substitution C T upstream_gene_variant MELA-AU 10 122666114 122666114 single base substitution T G 3_prime_UTR_variant MELA-AU 10 122666114 122666114 single base substitution T G downstream_gene_variant MELA-AU 10 122666114 122666114 single base substitution T G intron_variant MELA-AU 10 122666114 122666114 single base substitution T G upstream_gene_variant MELA-AU 10 122666128 122666128 single base substitution T A 3_prime_UTR_variant MELA-AU 10 122666128 122666128 single base substitution T A downstream_gene_variant MELA-AU 10 122666128 122666128 single base substitution T A intron_variant MELA-AU 10 122666128 122666128 single base substitution T A upstream_gene_variant MELA-AU 10 122666130 122666130 single base substitution C T 3_prime_UTR_variant MELA-AU 10 122666130 122666130 single base substitution C T downstream_gene_variant MELA-AU 10 122666130 122666130 single base substitution C T intron_variant MELA-AU 10 122666130 122666130 single base substitution C T upstream_gene_variant MELA-AU 10 122666372 122666372 single base substitution C T downstream_gene_variant MELA-AU 10 122666372 122666372 single base substitution C T splice_region_variant MELA-AU 10 122666372 122666372 single base substitution C T upstream_gene_variant MELA-AU 10 122666433 122666433 single base substitution C T downstream_gene_variant MELA-AU 10 122666433 122666433 single base substitution C T intron_variant MELA-AU 10 122666433 122666433 single base substitution C T upstream_gene_variant MELA-AU 10 122667170 122667170 single base substitution T A downstream_gene_variant MELA-AU 10 122667170 122667170 single base substitution T A exon_variant MELA-AU 10 122667170 122667170 single base substitution T A intron_variant MELA-AU 10 122667956 122667956 single base substitution C T downstream_gene_variant MELA-AU 10 122667956 122667956 single base substitution C T exon_variant MELA-AU 10 122667956 122667956 single base substitution C T intron_variant MELA-AU 10 122667957 122667957 single base substitution C T downstream_gene_variant MELA-AU 10 122667957 122667957 single base substitution C T exon_variant MELA-AU 10 122667957 122667957 single base substitution C T intron_variant MELA-AU 10 122668862 122668862 single base substitution T A 3_prime_UTR_variant MELA-AU 10 122668862 122668862 single base substitution T A downstream_gene_variant MELA-AU 10 122668862 122668862 single base substitution T A exon_variant MELA-AU 10 122669294 122669294 single base substitution C T downstream_gene_variant MELA-AU 10 122669305 122669305 single base substitution C T downstream_gene_variant MELA-AU 10 122669497 122669497 single base substitution C T downstream_gene_variant MELA-AU 10 122669519 122669519 single base substitution C T downstream_gene_variant MELA-AU 10 122669547 122669547 single base substitution C T downstream_gene_variant MELA-AU 10 122670445 122670445 single base substitution T C downstream_gene_variant MELA-AU 10 122670507 122670507 single base substitution C T downstream_gene_variant MELA-AU 10 122670811 122670811 single base substitution C T downstream_gene_variant MELA-AU 10 122671420 122671420 single base substitution C A downstream_gene_variant ORCA-IN 10 122625984 122625984 single base substitution G A downstream_gene_variant ORCA-IN 10 122625984 122625984 single base substitution G A intron_variant ORCA-IN 10 122625984 122625984 single base substitution G A upstream_gene_variant ORCA-IN 10 122640230 122640230 single base substitution A C intron_variant ORCA-IN 10 122640230 122640230 single base substitution A C upstream_gene_variant ORCA-IN 10 122664834 122664834 single base substitution G A 3_prime_UTR_variant ORCA-IN 10 122664834 122664834 single base substitution G A downstream_gene_variant ORCA-IN 10 122664834 122664834 single base substitution G A exon_variant ORCA-IN 10 122664834 122664834 single base substitution G A missense_variant G1066D 3197G>A ORCA-IN 10 122664834 122664834 single base substitution G A splice_region_variant ORCA-IN 10 122664834 122664834 single base substitution G A upstream_gene_variant ORCA-IN 10 122665401 122665401 single base substitution C A 3_prime_UTR_variant ORCA-IN 10 122665401 122665401 single base substitution C A downstream_gene_variant ORCA-IN 10 122665401 122665401 single base substitution C A exon_variant ORCA-IN 10 122665401 122665401 single base substitution C A missense_variant P1102H 3305C>A ORCA-IN 10 122665401 122665401 single base substitution C A upstream_gene_variant ORCA-IN 10 122665478 122665478 single base substitution C T 3_prime_UTR_variant ORCA-IN 10 122665478 122665478 single base substitution C T downstream_gene_variant ORCA-IN 10 122665478 122665478 single base substitution C T exon_variant ORCA-IN 10 122665478 122665478 single base substitution C T missense_variant L1128F 3382C>T ORCA-IN 10 122665478 122665478 single base substitution C T upstream_gene_variant OV-AU 10 122606974 122606974 single base substitution C T upstream_gene_variant OV-AU 10 122610805 122610805 single base substitution G A 5_prime_UTR_variant OV-AU 10 122610805 122610805 single base substitution G A upstream_gene_variant OV-AU 10 122610947 122610947 single base substitution A T exon_variant OV-AU 10 122610947 122610947 single base substitution A T synonymous_variant T5T 15A>T OV-AU 10 122610947 122610947 single base substitution A T upstream_gene_variant OV-AU 10 122614022 122614022 single base substitution C T intron_variant OV-AU 10 122616432 122616432 single base substitution G T intron_variant OV-AU 10 122632095 122632095 single base substitution A T intron_variant OV-AU 10 122634258 122634258 single base substitution T C intron_variant OV-AU 10 122634258 122634258 single base substitution T C upstream_gene_variant OV-AU 10 122651969 122651969 single base substitution A G downstream_gene_variant OV-AU 10 122651969 122651969 single base substitution A G intron_variant OV-AU 10 122655120 122655120 single base substitution A G intron_variant OV-AU 10 122655120 122655120 single base substitution A G upstream_gene_variant OV-AU 10 122655782 122655782 single base substitution A T intron_variant OV-AU 10 122655782 122655782 single base substitution A T upstream_gene_variant OV-AU 10 122658108 122658108 single base substitution G T intron_variant OV-AU 10 122658108 122658108 single base substitution G T upstream_gene_variant OV-AU 10 122658306 122658306 single base substitution C T intron_variant OV-AU 10 122658306 122658306 single base substitution C T upstream_gene_variant OV-AU 10 122662634 122662634 single base substitution C T 3_prime_UTR_variant OV-AU 10 122662634 122662634 single base substitution C T exon_variant OV-AU 10 122662634 122662634 single base substitution C T stop_gained Q941* 2821C>T OV-AU 10 122662634 122662634 single base substitution C T upstream_gene_variant OV-AU 10 122665644 122665644 single base substitution G C 3_prime_UTR_variant OV-AU 10 122665644 122665644 single base substitution G C downstream_gene_variant OV-AU 10 122665644 122665644 single base substitution G C intron_variant OV-AU 10 122665644 122665644 single base substitution G C upstream_gene_variant OV-AU 10 122666580 122666580 single base substitution G C downstream_gene_variant OV-AU 10 122666580 122666580 single base substitution G C intron_variant OV-AU 10 122666580 122666580 single base substitution G C upstream_gene_variant OV-AU 10 122669460 122669460 single base substitution G T downstream_gene_variant PACA-AU 10 122608666 122608666 single base substitution G A upstream_gene_variant PACA-AU 10 122612105 122612105 single base substitution A C 5_prime_UTR_variant PACA-AU 10 122612105 122612105 single base substitution A C exon_variant PACA-AU 10 122612105 122612105 single base substitution A C intron_variant PACA-AU 10 122612105 122612105 single base substitution A C missense_variant Q52H 156A>C PACA-AU 10 122612105 122612105 single base substitution A C upstream_gene_variant PACA-AU 10 122615783 122615783 single base substitution A G intron_variant PACA-AU 10 122616246 122616246 single base substitution T A intron_variant PACA-AU 10 122616975 122616975 single base substitution T C intron_variant PACA-AU 10 122616975 122616975 single base substitution T C upstream_gene_variant PACA-AU 10 122618547 122618547 single base substitution A G downstream_gene_variant PACA-AU 10 122618547 122618547 single base substitution A G intron_variant PACA-AU 10 122618547 122618547 single base substitution A G upstream_gene_variant PACA-AU 10 122625478 122625478 single base substitution G T downstream_gene_variant PACA-AU 10 122625478 122625478 single base substitution G T intron_variant PACA-AU 10 122625478 122625478 single base substitution G T upstream_gene_variant PACA-AU 10 122625984 122625984 single base substitution G A downstream_gene_variant PACA-AU 10 122625984 122625984 single base substitution G A intron_variant PACA-AU 10 122625984 122625984 single base substitution G A upstream_gene_variant PACA-AU 10 122628932 122628932 single base substitution A C downstream_gene_variant PACA-AU 10 122628932 122628932 single base substitution A C intron_variant PACA-AU 10 122631020 122631020 deletion of <=200bp T - intron_variant PACA-AU 10 122631556 122631556 single base substitution C G intron_variant PACA-AU 10 122638416 122638416 single base substitution G A intron_variant PACA-AU 10 122638416 122638416 single base substitution G A upstream_gene_variant PACA-AU 10 122640311 122640311 single base substitution C T intron_variant PACA-AU 10 122640311 122640311 single base substitution C T upstream_gene_variant PACA-AU 10 122644804 122644804 single base substitution C T downstream_gene_variant PACA-AU 10 122644804 122644804 single base substitution C T intron_variant PACA-AU 10 122644804 122644804 single base substitution C T upstream_gene_variant PACA-AU 10 122648311 122648311 single base substitution T C downstream_gene_variant PACA-AU 10 122648311 122648311 single base substitution T C intron_variant PACA-AU 10 122648751 122648751 insertion of <=200bp - TTTTGTTTTG exon_variant PACA-AU 10 122648751 122648751 insertion of <=200bp - TTTTGTTTTG intron_variant PACA-AU 10 122649911 122649911 single base substitution A G downstream_gene_variant PACA-AU 10 122649911 122649911 single base substitution A G intron_variant PACA-AU 10 122660780 122660780 single base substitution G A intron_variant PACA-AU 10 122660780 122660780 single base substitution G A upstream_gene_variant PACA-AU 10 122661578 122661578 single base substitution G T intron_variant PACA-AU 10 122661578 122661578 single base substitution G T upstream_gene_variant PACA-AU 10 122667219 122667219 single base substitution C T downstream_gene_variant PACA-AU 10 122667219 122667219 single base substitution C T exon_variant PACA-AU 10 122667219 122667219 single base substitution C T intron_variant PACA-CA 10 122613292 122613292 single base substitution G A intron_variant PACA-CA 10 122615124 122615124 single base substitution T C intron_variant PACA-CA 10 122617067 122617067 single base substitution A T intron_variant PACA-CA 10 122617067 122617067 single base substitution A T upstream_gene_variant PACA-CA 10 122625160 122625160 single base substitution C T downstream_gene_variant PACA-CA 10 122625160 122625160 single base substitution C T exon_variant PACA-CA 10 122625160 122625160 single base substitution C T intron_variant PACA-CA 10 122625160 122625160 single base substitution C T missense_variant R300C 898C>T PACA-CA 10 122625160 122625160 single base substitution C T missense_variant R41C 121C>T PACA-CA 10 122625160 122625160 single base substitution C T upstream_gene_variant PACA-CA 10 122629677 122629677 single base substitution G A downstream_gene_variant PACA-CA 10 122629677 122629677 single base substitution G A intron_variant PACA-CA 10 122630715 122630715 single base substitution G A exon_variant PACA-CA 10 122630715 122630715 single base substitution G A intron_variant PACA-CA 10 122630715 122630715 single base substitution G A missense_variant R184K 551G>A PACA-CA 10 122630715 122630715 single base substitution G A missense_variant R443K 1328G>A PACA-CA 10 122644229 122644229 single base substitution G C downstream_gene_variant PACA-CA 10 122644229 122644229 single base substitution G C intron_variant PACA-CA 10 122644229 122644229 single base substitution G C upstream_gene_variant PACA-CA 10 122651755 122651755 single base substitution G C downstream_gene_variant PACA-CA 10 122651755 122651755 single base substitution G C intron_variant PACA-CA 10 122653755 122653755 single base substitution G C downstream_gene_variant PACA-CA 10 122653755 122653755 single base substitution G C intron_variant PACA-CA 10 122656039 122656039 insertion of <=200bp - CA intron_variant PACA-CA 10 122656039 122656039 insertion of <=200bp - CA upstream_gene_variant PACA-CA 10 122656083 122656083 insertion of <=200bp - T intron_variant PACA-CA 10 122656083 122656083 insertion of <=200bp - T upstream_gene_variant PACA-CA 10 122663585 122663585 single base substitution G A 3_prime_UTR_variant PACA-CA 10 122663585 122663585 single base substitution G A downstream_gene_variant PACA-CA 10 122663585 122663585 single base substitution G A exon_variant PACA-CA 10 122663585 122663585 single base substitution G A synonymous_variant L986L 2958G>A PACA-CA 10 122663585 122663585 single base substitution G A upstream_gene_variant PACA-CA 10 122663706 122663706 single base substitution G A downstream_gene_variant PACA-CA 10 122663706 122663706 single base substitution G A intron_variant PACA-CA 10 122663706 122663706 single base substitution G A upstream_gene_variant PACA-CA 10 122668644 122668645 deletion of <=200bp AC - 3_prime_UTR_variant PACA-CA 10 122668644 122668645 deletion of <=200bp AC - downstream_gene_variant PACA-CA 10 122668644 122668645 deletion of <=200bp AC - exon_variant PAEN-AU 10 122628932 122628932 single base substitution A C downstream_gene_variant PAEN-AU 10 122628932 122628932 single base substitution A C intron_variant PAEN-AU 10 122632738 122632738 single base substitution A G intron_variant PAEN-AU 10 122638745 122638745 single base substitution A G exon_variant PAEN-AU 10 122638745 122638745 single base substitution A G intron_variant PAEN-AU 10 122646266 122646266 single base substitution T A 3_prime_UTR_variant PAEN-AU 10 122646266 122646266 single base substitution T A downstream_gene_variant PAEN-AU 10 122646266 122646266 single base substitution T A exon_variant PAEN-AU 10 122646266 122646266 single base substitution T A missense_variant V680E 2039T>A PAEN-IT 10 122639237 122639237 single base substitution G A exon_variant PAEN-IT 10 122639237 122639237 single base substitution G A intron_variant PBCA-DE 10 122608043 122608044 deletion of <=200bp CA - upstream_gene_variant PBCA-DE 10 122617338 122617338 single base substitution C T intron_variant PBCA-DE 10 122617338 122617338 single base substitution C T upstream_gene_variant PBCA-DE 10 122617646 122617646 deletion of <=200bp T - intron_variant PBCA-DE 10 122617646 122617646 deletion of <=200bp T - upstream_gene_variant PBCA-DE 10 122625223 122625223 single base substitution A T downstream_gene_variant PBCA-DE 10 122625223 122625223 single base substitution A T exon_variant PBCA-DE 10 122625223 122625223 single base substitution A T intron_variant PBCA-DE 10 122625223 122625223 single base substitution A T missense_variant N321Y 961A>T PBCA-DE 10 122625223 122625223 single base substitution A T missense_variant N62Y 184A>T PBCA-DE 10 122625223 122625223 single base substitution A T upstream_gene_variant PBCA-DE 10 122644275 122644275 single base substitution C T downstream_gene_variant PBCA-DE 10 122644275 122644275 single base substitution C T intron_variant PBCA-DE 10 122644275 122644275 single base substitution C T upstream_gene_variant PBCA-DE 10 122644784 122644785 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 10 122644784 122644785 deletion of <=200bp TA - intron_variant PBCA-DE 10 122644784 122644785 deletion of <=200bp TA - upstream_gene_variant PBCA-DE 10 122654699 122654699 single base substitution G C intron_variant PBCA-DE 10 122654699 122654699 single base substitution G C upstream_gene_variant PBCA-DE 10 122658920 122658920 single base substitution G C intron_variant PBCA-DE 10 122658920 122658920 single base substitution G C upstream_gene_variant PBCA-DE 10 122660320 122660320 single base substitution G T intron_variant PBCA-DE 10 122660320 122660320 single base substitution G T upstream_gene_variant PRAD-CA 10 122608670 122608670 single base substitution G T upstream_gene_variant PRAD-CA 10 122618784 122618784 single base substitution C T downstream_gene_variant PRAD-CA 10 122618784 122618784 single base substitution C T intron_variant PRAD-CA 10 122618784 122618784 single base substitution C T upstream_gene_variant PRAD-CA 10 122629555 122629555 single base substitution C T downstream_gene_variant PRAD-CA 10 122629555 122629555 single base substitution C T intron_variant PRAD-CA 10 122639197 122639197 single base substitution T C exon_variant PRAD-CA 10 122639197 122639197 single base substitution T C intron_variant PRAD-CA 10 122649287 122649287 single base substitution A G exon_variant PRAD-CA 10 122649287 122649287 single base substitution A G intron_variant PRAD-CA 10 122663233 122663233 single base substitution C T downstream_gene_variant PRAD-CA 10 122663233 122663233 single base substitution C T intron_variant PRAD-CA 10 122663233 122663233 single base substitution C T upstream_gene_variant PRAD-CA 10 122665805 122665805 single base substitution G C 3_prime_UTR_variant PRAD-CA 10 122665805 122665805 single base substitution G C downstream_gene_variant PRAD-CA 10 122665805 122665805 single base substitution G C intron_variant PRAD-CA 10 122665805 122665805 single base substitution G C upstream_gene_variant PRAD-UK 10 122617505 122617505 single base substitution A C intron_variant PRAD-UK 10 122617505 122617505 single base substitution A C upstream_gene_variant PRAD-UK 10 122629526 122629526 single base substitution T A downstream_gene_variant PRAD-UK 10 122629526 122629526 single base substitution T A intron_variant PRAD-UK 10 122632842 122632842 single base substitution G T intron_variant PRAD-UK 10 122633982 122633982 single base substitution G C intron_variant PRAD-UK 10 122633982 122633982 single base substitution G C upstream_gene_variant PRAD-UK 10 122635724 122635724 single base substitution T C intron_variant PRAD-UK 10 122635724 122635724 single base substitution T C upstream_gene_variant PRAD-UK 10 122638435 122638435 single base substitution A G intron_variant PRAD-UK 10 122638435 122638435 single base substitution A G upstream_gene_variant PRAD-UK 10 122638595 122638595 insertion of <=200bp - T exon_variant PRAD-UK 10 122638595 122638595 insertion of <=200bp - T intron_variant PRAD-UK 10 122639160 122639160 single base substitution G A exon_variant PRAD-UK 10 122639160 122639160 single base substitution G A intron_variant PRAD-UK 10 122640921 122640921 single base substitution A T downstream_gene_variant PRAD-UK 10 122640921 122640921 single base substitution A T intron_variant PRAD-UK 10 122640921 122640921 single base substitution A T upstream_gene_variant PRAD-UK 10 122651522 122651522 single base substitution A G downstream_gene_variant PRAD-UK 10 122651522 122651522 single base substitution A G intron_variant PRAD-UK 10 122665480 122665480 single base substitution C T 3_prime_UTR_variant PRAD-UK 10 122665480 122665480 single base substitution C T downstream_gene_variant PRAD-UK 10 122665480 122665480 single base substitution C T exon_variant PRAD-UK 10 122665480 122665480 single base substitution C T synonymous_variant L1128L 3384C>T PRAD-UK 10 122665480 122665480 single base substitution C T upstream_gene_variant PRAD-UK 10 122671397 122671397 deletion of <=200bp G - downstream_gene_variant PRAD-US 10 122646216 122646219 deletion of <=200bp AGAA - 3_prime_UTR_variant PRAD-US 10 122646216 122646219 deletion of <=200bp AGAA - downstream_gene_variant PRAD-US 10 122646216 122646219 deletion of <=200bp AGAA - exon_variant PRAD-US 10 122646216 122646219 deletion of <=200bp AGAA - frameshift_variant AE663 PRAD-US 10 122662580 122662580 single base substitution G T 3_prime_UTR_variant PRAD-US 10 122662580 122662580 single base substitution G T exon_variant PRAD-US 10 122662580 122662580 single base substitution G T stop_gained E923* 2767G>T PRAD-US 10 122662580 122662580 single base substitution G T upstream_gene_variant RECA-EU 10 122610461 122610461 single base substitution A C upstream_gene_variant RECA-EU 10 122627992 122627992 single base substitution T G downstream_gene_variant RECA-EU 10 122627992 122627992 single base substitution T G intron_variant RECA-EU 10 122627992 122627992 single base substitution T G upstream_gene_variant RECA-EU 10 122637793 122637793 single base substitution A G intron_variant RECA-EU 10 122637793 122637793 single base substitution A G upstream_gene_variant RECA-EU 10 122639900 122639900 single base substitution C T exon_variant RECA-EU 10 122639900 122639900 single base substitution C T intron_variant RECA-EU 10 122639900 122639900 single base substitution C T upstream_gene_variant RECA-EU 10 122652836 122652836 single base substitution T G downstream_gene_variant RECA-EU 10 122652836 122652836 single base substitution T G intron_variant RECA-EU 10 122658480 122658480 single base substitution C T intron_variant RECA-EU 10 122658480 122658480 single base substitution C T upstream_gene_variant RECA-EU 10 122662847 122662847 single base substitution C A downstream_gene_variant RECA-EU 10 122662847 122662847 single base substitution C A intron_variant RECA-EU 10 122662847 122662847 single base substitution C A upstream_gene_variant SKCA-BR 10 122606836 122606836 single base substitution C G upstream_gene_variant SKCA-BR 10 122606840 122606840 single base substitution C T upstream_gene_variant SKCA-BR 10 122606906 122606906 single base substitution G A upstream_gene_variant SKCA-BR 10 122607877 122607877 single base substitution T C upstream_gene_variant SKCA-BR 10 122607921 122607921 single base substitution C G upstream_gene_variant SKCA-BR 10 122613544 122613544 single base substitution C G intron_variant SKCA-BR 10 122614641 122614641 single base substitution T A intron_variant SKCA-BR 10 122616062 122616062 single base substitution C G intron_variant SKCA-BR 10 122628334 122628334 single base substitution C T downstream_gene_variant SKCA-BR 10 122628334 122628334 single base substitution C T intron_variant SKCA-BR 10 122628616 122628617 deletion of <=200bp AG - downstream_gene_variant SKCA-BR 10 122628616 122628617 deletion of <=200bp AG - intron_variant SKCA-BR 10 122628618 122628618 single base substitution G T downstream_gene_variant SKCA-BR 10 122628618 122628618 single base substitution G T intron_variant SKCA-BR 10 122628653 122628653 single base substitution T C downstream_gene_variant SKCA-BR 10 122628653 122628653 single base substitution T C intron_variant SKCA-BR 10 122629297 122629297 insertion of <=200bp - TTTTTA downstream_gene_variant SKCA-BR 10 122629297 122629297 insertion of <=200bp - TTTTTA intron_variant SKCA-BR 10 122633688 122633688 insertion of <=200bp - GTTTTT intron_variant SKCA-BR 10 122633688 122633688 insertion of <=200bp - GTTTTT upstream_gene_variant SKCA-BR 10 122633729 122633729 single base substitution G T intron_variant SKCA-BR 10 122633729 122633729 single base substitution G T upstream_gene_variant SKCA-BR 10 122633739 122633739 single base substitution G T intron_variant SKCA-BR 10 122633739 122633739 single base substitution G T upstream_gene_variant SKCA-BR 10 122638755 122638755 single base substitution T A exon_variant SKCA-BR 10 122638755 122638755 single base substitution T A intron_variant SKCA-BR 10 122640864 122640864 single base substitution C T downstream_gene_variant SKCA-BR 10 122640864 122640864 single base substitution C T intron_variant SKCA-BR 10 122640864 122640864 single base substitution C T upstream_gene_variant SKCA-BR 10 122642647 122642647 single base substitution G A downstream_gene_variant SKCA-BR 10 122642647 122642647 single base substitution G A intron_variant SKCA-BR 10 122642647 122642647 single base substitution G A upstream_gene_variant SKCA-BR 10 122644135 122644135 single base substitution C A downstream_gene_variant SKCA-BR 10 122644135 122644135 single base substitution C A intron_variant SKCA-BR 10 122644135 122644135 single base substitution C A upstream_gene_variant SKCA-BR 10 122648750 122648750 insertion of <=200bp - TTTTTGTTTTG exon_variant SKCA-BR 10 122648750 122648750 insertion of <=200bp - TTTTTGTTTTG intron_variant SKCA-BR 10 122655759 122655759 single base substitution T C intron_variant SKCA-BR 10 122655759 122655759 single base substitution T C upstream_gene_variant SKCA-BR 10 122656323 122656323 single base substitution A G intron_variant SKCA-BR 10 122656323 122656323 single base substitution A G upstream_gene_variant SKCA-BR 10 122666084 122666084 single base substitution T A 3_prime_UTR_variant SKCA-BR 10 122666084 122666084 single base substitution T A downstream_gene_variant SKCA-BR 10 122666084 122666084 single base substitution T A intron_variant SKCA-BR 10 122666084 122666084 single base substitution T A upstream_gene_variant SKCA-BR 10 122667114 122667114 insertion of <=200bp - ATT downstream_gene_variant SKCA-BR 10 122667114 122667114 insertion of <=200bp - ATT exon_variant SKCA-BR 10 122667114 122667114 insertion of <=200bp - ATT intron_variant SKCA-BR 10 122668544 122668544 single base substitution C T 3_prime_UTR_variant SKCA-BR 10 122668544 122668544 single base substitution C T downstream_gene_variant SKCA-BR 10 122668544 122668544 single base substitution C T exon_variant SKCA-BR 10 122670338 122670338 single base substitution C T downstream_gene_variant SKCA-BR 10 122670908 122670908 single base substitution A G downstream_gene_variant SKCA-BR 10 122670970 122670970 single base substitution G T downstream_gene_variant SKCA-BR 10 122671476 122671476 single base substitution G C downstream_gene_variant SKCA-BR 10 122672860 122672860 single base substitution A C downstream_gene_variant SKCA-BR 10 122673155 122673155 single base substitution C G downstream_gene_variant SKCA-BR 10 122673211 122673211 single base substitution C A downstream_gene_variant SKCA-BR 10 122673804 122673804 single base substitution C G downstream_gene_variant SKCA-BR 10 122674010 122674010 single base substitution T C downstream_gene_variant SKCM-US 10 122612140 122612140 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 122612140 122612140 single base substitution T C exon_variant SKCM-US 10 122612140 122612140 single base substitution T C intron_variant SKCM-US 10 122612140 122612140 single base substitution T C missense_variant V64A 191T>C SKCM-US 10 122618232 122618232 single base substitution T C 5_prime_UTR_variant SKCM-US 10 122618232 122618232 single base substitution T C exon_variant SKCM-US 10 122618232 122618232 single base substitution T C intron_variant SKCM-US 10 122618232 122618232 single base substitution T C synonymous_variant N92N 276T>C SKCM-US 10 122618232 122618232 single base substitution T C upstream_gene_variant SKCM-US 10 122622429 122622429 single base substitution C T 5_prime_UTR_variant SKCM-US 10 122622429 122622429 single base substitution C T downstream_gene_variant SKCM-US 10 122622429 122622429 single base substitution C T exon_variant SKCM-US 10 122622429 122622429 single base substitution C T intron_variant SKCM-US 10 122622429 122622429 single base substitution C T missense_variant P237S 709C>T SKCM-US 10 122624714 122624714 single base substitution C T downstream_gene_variant SKCM-US 10 122624714 122624714 single base substitution C T exon_variant SKCM-US 10 122624714 122624714 single base substitution C T intron_variant SKCM-US 10 122624714 122624714 single base substitution C T missense_variant P290L 869C>T SKCM-US 10 122624714 122624714 single base substitution C T missense_variant P31L 92C>T SKCM-US 10 122624714 122624714 single base substitution C T upstream_gene_variant SKCM-US 10 122625192 122625192 single base substitution T C downstream_gene_variant SKCM-US 10 122625192 122625192 single base substitution T C exon_variant SKCM-US 10 122625192 122625192 single base substitution T C intron_variant SKCM-US 10 122625192 122625192 single base substitution T C synonymous_variant G310G 930T>C SKCM-US 10 122625192 122625192 single base substitution T C synonymous_variant G51G 153T>C SKCM-US 10 122625192 122625192 single base substitution T C upstream_gene_variant SKCM-US 10 122626202 122626202 single base substitution C T downstream_gene_variant SKCM-US 10 122626202 122626202 single base substitution C T exon_variant SKCM-US 10 122626202 122626202 single base substitution C T intron_variant SKCM-US 10 122626202 122626202 single base substitution C T synonymous_variant A113A 339C>T SKCM-US 10 122626202 122626202 single base substitution C T synonymous_variant A372A 1116C>T SKCM-US 10 122626202 122626202 single base substitution C T upstream_gene_variant SKCM-US 10 122630798 122630798 single base substitution C T exon_variant SKCM-US 10 122630798 122630798 single base substitution C T missense_variant R212C 634C>T SKCM-US 10 122630798 122630798 single base substitution C T missense_variant R471C 1411C>T SKCM-US 10 122648694 122648694 single base substitution C T exon_variant SKCM-US 10 122648694 122648694 single base substitution C T splice_region_variant SKCM-US 10 122664262 122664262 single base substitution C T 3_prime_UTR_variant SKCM-US 10 122664262 122664262 single base substitution C T downstream_gene_variant SKCM-US 10 122664262 122664262 single base substitution C T exon_variant SKCM-US 10 122664262 122664262 single base substitution C T intron_variant SKCM-US 10 122664262 122664262 single base substitution C T synonymous_variant G1044G 3132C>T SKCM-US 10 122664262 122664262 single base substitution C T upstream_gene_variant SKCM-US 10 122665478 122665478 single base substitution C T 3_prime_UTR_variant SKCM-US 10 122665478 122665478 single base substitution C T downstream_gene_variant SKCM-US 10 122665478 122665478 single base substitution C T exon_variant SKCM-US 10 122665478 122665478 single base substitution C T missense_variant L1128F 3382C>T SKCM-US 10 122665478 122665478 single base substitution C T upstream_gene_variant SKCM-US 10 122665480 122665480 single base substitution C T 3_prime_UTR_variant SKCM-US 10 122665480 122665480 single base substitution C T downstream_gene_variant SKCM-US 10 122665480 122665480 single base substitution C T exon_variant SKCM-US 10 122665480 122665480 single base substitution C T synonymous_variant L1128L 3384C>T SKCM-US 10 122665480 122665480 single base substitution C T upstream_gene_variant STAD-US 10 122622315 122622315 insertion of <=200bp - A 5_prime_UTR_variant STAD-US 10 122622315 122622315 insertion of <=200bp - A downstream_gene_variant STAD-US 10 122622315 122622315 insertion of <=200bp - A exon_variant STAD-US 10 122622315 122622315 insertion of <=200bp - A frameshift_variant K199K? STAD-US 10 122622315 122622315 insertion of <=200bp - A intron_variant STAD-US 10 122624600 122624600 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant STAD-US 10 122624600 122624600 single base substitution A G downstream_gene_variant STAD-US 10 122624600 122624600 single base substitution A G exon_variant STAD-US 10 122624600 122624600 single base substitution A G intron_variant STAD-US 10 122624600 122624600 single base substitution A G missense_variant Y252C 755A>G STAD-US 10 122624600 122624600 single base substitution A G upstream_gene_variant STAD-US 10 122625206 122625206 single base substitution G A downstream_gene_variant STAD-US 10 122625206 122625206 single base substitution G A exon_variant STAD-US 10 122625206 122625206 single base substitution G A intron_variant STAD-US 10 122625206 122625206 single base substitution G A missense_variant R315H 944G>A STAD-US 10 122625206 122625206 single base substitution G A missense_variant R56H 167G>A STAD-US 10 122625206 122625206 single base substitution G A upstream_gene_variant STAD-US 10 122626116 122626116 single base substitution C T downstream_gene_variant STAD-US 10 122626116 122626116 single base substitution C T exon_variant STAD-US 10 122626116 122626116 single base substitution C T intron_variant STAD-US 10 122626116 122626116 single base substitution C T stop_gained R344* 1030C>T STAD-US 10 122626116 122626116 single base substitution C T stop_gained R85* 253C>T STAD-US 10 122626116 122626116 single base substitution C T upstream_gene_variant STAD-US 10 122645359 122645359 single base substitution A G 3_prime_UTR_variant STAD-US 10 122645359 122645359 single base substitution A G downstream_gene_variant STAD-US 10 122645359 122645359 single base substitution A G exon_variant STAD-US 10 122645359 122645359 single base substitution A G missense_variant R628G 1882A>G STAD-US 10 122645359 122645359 single base substitution A G upstream_gene_variant STAD-US 10 122660586 122660586 single base substitution A G 3_prime_UTR_variant STAD-US 10 122660586 122660586 single base substitution A G exon_variant STAD-US 10 122660586 122660586 single base substitution A G missense_variant Q888R 2663A>G STAD-US 10 122660586 122660586 single base substitution A G upstream_gene_variant STAD-US 10 122661812 122661812 single base substitution C T 3_prime_UTR_variant STAD-US 10 122661812 122661812 single base substitution C T exon_variant STAD-US 10 122661812 122661812 single base substitution C T stop_gained Q911* 2731C>T STAD-US 10 122661812 122661812 single base substitution C T upstream_gene_variant STAD-US 10 122665505 122665505 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 10 122665505 122665505 deletion of <=200bp T - downstream_gene_variant STAD-US 10 122665505 122665505 deletion of <=200bp T - exon_variant STAD-US 10 122665505 122665505 deletion of <=200bp T - frameshift_variant F1137 STAD-US 10 122665505 122665505 deletion of <=200bp T - upstream_gene_variant THCA-US 10 122612090 122612090 single base substitution T G 5_prime_UTR_variant THCA-US 10 122612090 122612090 single base substitution T G exon_variant THCA-US 10 122612090 122612090 single base substitution T G intron_variant THCA-US 10 122612090 122612090 single base substitution T G missense_variant D47E 141T>G THCA-US 10 122612090 122612090 single base substitution T G upstream_gene_variant THCA-US 10 122619684 122619684 single base substitution A G 5_prime_UTR_variant THCA-US 10 122619684 122619684 single base substitution A G downstream_gene_variant THCA-US 10 122619684 122619684 single base substitution A G exon_variant THCA-US 10 122619684 122619684 single base substitution A G intron_variant THCA-US 10 122619684 122619684 single base substitution A G missense_variant N139S 416A>G THCA-US 10 122619684 122619684 single base substitution A G upstream_gene_variant UCEC-US 10 122618293 122618293 single base substitution G A 5_prime_UTR_variant UCEC-US 10 122618293 122618293 single base substitution G A exon_variant UCEC-US 10 122618293 122618293 single base substitution G A intron_variant UCEC-US 10 122618293 122618293 single base substitution G A missense_variant A113T 337G>A UCEC-US 10 122618293 122618293 single base substitution G A upstream_gene_variant UCEC-US 10 122619655 122619655 single base substitution C T 5_prime_UTR_variant UCEC-US 10 122619655 122619655 single base substitution C T downstream_gene_variant UCEC-US 10 122619655 122619655 single base substitution C T exon_variant UCEC-US 10 122619655 122619655 single base substitution C T intron_variant UCEC-US 10 122619655 122619655 single base substitution C T synonymous_variant R129R 387C>T UCEC-US 10 122619655 122619655 single base substitution C T upstream_gene_variant UCEC-US 10 122619707 122619707 single base substitution G A 5_prime_UTR_variant UCEC-US 10 122619707 122619707 single base substitution G A downstream_gene_variant UCEC-US 10 122619707 122619707 single base substitution G A exon_variant UCEC-US 10 122619707 122619707 single base substitution G A intron_variant UCEC-US 10 122619707 122619707 single base substitution G A missense_variant D147N 439G>A UCEC-US 10 122619707 122619707 single base substitution G A upstream_gene_variant UCEC-US 10 122619762 122619762 single base substitution C A 5_prime_UTR_variant UCEC-US 10 122619762 122619762 single base substitution C A downstream_gene_variant UCEC-US 10 122619762 122619762 single base substitution C A exon_variant UCEC-US 10 122619762 122619762 single base substitution C A intron_variant UCEC-US 10 122619762 122619762 single base substitution C A missense_variant S165Y 494C>A UCEC-US 10 122619762 122619762 single base substitution C A upstream_gene_variant UCEC-US 10 122622323 122622323 single base substitution T G 5_prime_UTR_variant UCEC-US 10 122622323 122622323 single base substitution T G downstream_gene_variant UCEC-US 10 122622323 122622323 single base substitution T G exon_variant UCEC-US 10 122622323 122622323 single base substitution T G intron_variant UCEC-US 10 122622323 122622323 single base substitution T G synonymous_variant V201V 603T>G UCEC-US 10 122630798 122630798 single base substitution C T exon_variant UCEC-US 10 122630798 122630798 single base substitution C T missense_variant R212C 634C>T UCEC-US 10 122630798 122630798 single base substitution C T missense_variant R471C 1411C>T UCEC-US 10 122633379 122633379 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122633379 122633379 single base substitution C T exon_variant UCEC-US 10 122633379 122633379 single base substitution C T synonymous_variant Y241Y 723C>T UCEC-US 10 122633379 122633379 single base substitution C T synonymous_variant Y500Y 1500C>T UCEC-US 10 122640387 122640387 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122640387 122640387 single base substitution C T exon_variant UCEC-US 10 122640387 122640387 single base substitution C T synonymous_variant I312I 936C>T UCEC-US 10 122640387 122640387 single base substitution C T synonymous_variant I571I 1713C>T UCEC-US 10 122640387 122640387 single base substitution C T upstream_gene_variant UCEC-US 10 122643396 122643396 single base substitution C A 3_prime_UTR_variant UCEC-US 10 122643396 122643396 single base substitution C A downstream_gene_variant UCEC-US 10 122643396 122643396 single base substitution C A exon_variant UCEC-US 10 122643396 122643396 single base substitution C A missense_variant A615D 1844C>A UCEC-US 10 122643396 122643396 single base substitution C A upstream_gene_variant UCEC-US 10 122646251 122646251 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122646251 122646251 single base substitution C T downstream_gene_variant UCEC-US 10 122646251 122646251 single base substitution C T exon_variant UCEC-US 10 122646251 122646251 single base substitution C T missense_variant A675V 2024C>T UCEC-US 10 122649475 122649475 single base substitution T G 3_prime_UTR_variant UCEC-US 10 122649475 122649475 single base substitution T G exon_variant UCEC-US 10 122649475 122649475 single base substitution T G stop_gained L766* 2297T>G UCEC-US 10 122650298 122650298 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122650298 122650298 single base substitution C T downstream_gene_variant UCEC-US 10 122650298 122650298 single base substitution C T intron_variant UCEC-US 10 122650298 122650298 single base substitution C T missense_variant T805M 2414C>T UCEC-US 10 122650367 122650367 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122650367 122650367 single base substitution C T downstream_gene_variant UCEC-US 10 122650367 122650367 single base substitution C T intron_variant UCEC-US 10 122650367 122650367 single base substitution C T missense_variant A828V 2483C>T UCEC-US 10 122665427 122665427 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122665427 122665427 single base substitution C T downstream_gene_variant UCEC-US 10 122665427 122665427 single base substitution C T exon_variant UCEC-US 10 122665427 122665427 single base substitution C T missense_variant R1111W 3331C>T UCEC-US 10 122665427 122665427 single base substitution C T upstream_gene_variant UCEC-US 10 122668142 122668142 single base substitution C T 3_prime_UTR_variant UCEC-US 10 122668142 122668142 single base substitution C T downstream_gene_variant UCEC-US 10 122668142 122668142 single base substitution C T exon_variant UCEC-US 10 122668142 122668142 single base substitution C T missense_variant L1198F 3592C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LS174T COSM2056014 c.871delT p.L292fs*3 Deletion - Frameshift 10:120865204-120865204 + TCGA-AP-A0LM-01 COSM915459 c.1844C>A p.A615D Substitution - Missense 10:120883884-120883884 + In-7 COSM144848 c.3469G>A p.V1157M Substitution - Missense 10:120906807-120906807 + Pat_01_B COSM5836365 c.2252G>T p.W751L Substitution - Missense 10:120889918-120889918 + TCGA-AX-A05Z-01 COSM242242 c.439G>A p.D147N Substitution - Missense 10:120860195-120860195 + TCGA-DK-A1AA-01 COSM1296999 c.465G>C p.K155N Substitution - Missense 10:120860221-120860221 + TCGA-FS-A1ZZ-06 COSM3434703 c.3384C>T p.L1128L Substitution - coding silent 10:120905968-120905968 + TCGA-AZ-4315-01 COSM1346181 c.3592C>A p.L1198I Substitution - Missense 10:120908630-120908630 + HCT116 COSM2056018 c.939_940delTT p.L314fs*7 Deletion - Frameshift 10:120865689-120865690 + PCSI_0083_Pa_P COSM2056015 c.898C>T p.R300C Substitution - Missense 10:120865648-120865648 + TCGA-AM-5820-01 COSM3751572 c.1542C>T p.H514H Substitution - coding silent 10:120873909-120873909 + CHC469T COSM3666664 c.683T>C p.V228A Substitution - Missense 10:120862891-120862891 + TCGA-A6-6780-01 COSM1346179 c.3234C>T p.D1078D Substitution - coding silent 10:120905359-120905359 + CHC433T COSM3747140 c.1664-10G>T p.? Unknown 10:120880816-120880816 + RKO COSM4647130 c.3351T>C p.C1117C Substitution - coding silent 10:120905935-120905935 + TCGA-DJ-A4V5-01 COSM3367922 c.141T>G p.D47E Substitution - Missense 10:120852578-120852578 + SNUH_G76_S1 COSM147068 c.2304A>G p.A768A Substitution - coding silent 10:120889970-120889970 + RMH004-R8 COSM4411235 c.1783T>A p.W595R Substitution - Missense 10:120883823-120883823 + Pat_40_B COSM5836364 c.2026C>T p.R676W Substitution - Missense 10:120886741-120886741 + LS180 COSM2056014 c.871delT p.L292fs*3 Deletion - Frameshift 10:120865204-120865204 + tumor_4119279 COSM5947048 c.92G>T p.W31L Substitution - Missense 10:120852529-120852529 + TCGA-FW-A3R5-06 COSM2056023 c.1116C>T p.A372A Substitution - coding silent 10:120866690-120866690 + GC8_T COSM147068 c.2304A>G p.A768A Substitution - coding silent 10:120889970-120889970 + HCC074T COSM5810161 c.2968A>T p.K990* Substitution - Nonsense 10:120904083-120904083 + TCGA-BR-A4QL-01 COSM4012138 c.1882A>G p.R628G Substitution - Missense 10:120885847-120885847 + TCGA-AP-A059-01 COSM915457 c.1500C>T p.Y500Y Substitution - coding silent 10:120873867-120873867 + LC_C9 COSM1188067 c.1052G>T p.R351M Substitution - Missense 10:120866626-120866626 + TCGA-FD-A3SN-01 COSM3790528 c.1654C>T p.L552F Substitution - Missense 10:120878450-120878450 + WA10 COSM242243 c.1502A>G p.H501R Substitution - Missense 10:120873869-120873869 + TCGA-09-1674-01 COSM1321499 c.2944G>C p.E982Q Substitution - Missense 10:120904059-120904059 + TCGA-E9-A22D-01 COSM1474405 c.275A>G p.N92S Substitution - Missense 10:120858719-120858719 + TCGA-AA-3833-01 COSM271603 c.3203A>G p.Q1068R Substitution - Missense 10:120905328-120905328 + JVM-2 COSM1739689 c.1987G>A p.A663T Substitution - Missense 10:120886702-120886702 + TCGA-AT-A5NU-01 COSM4414127 c.3397T>A p.S1133T Substitution - Missense 10:120905981-120905981 + RMH004-R2 COSM4411235 c.1783T>A p.W595R Substitution - Missense 10:120883823-120883823 + OSCC-GB_00940111 COSM4891610 c.3305C>A p.P1102H Substitution - Missense 10:120905889-120905889 + TCGA-B5-A0K9-01 COSM915461 c.2164A>G p.T722A Substitution - Missense 10:120889120-120889120 + TCGA-BR-6802-01 COSM4012136 c.944G>A p.R315H Substitution - Missense 10:120865694-120865694 + TCGA-RP-A695-06 COSM4896898 c.2226C>T p.S742S Substitution - coding silent 10:120889182-120889182 + TCGA-BS-A0TC-01 COSM915454 c.494C>A p.S165Y Substitution - Missense 10:120860250-120860250 + TCGA-AP-A0LM-01 COSM915456 c.1411C>T p.R471C Substitution - Missense 10:120871286-120871286 + AOCS-120-3-6 COSM4422325 c.15A>T p.T5T Substitution - coding silent 10:120851435-120851435 + TCGA-QB-A6FS-06 COSM3866641 c.276T>C p.N92N Substitution - coding silent 10:120858720-120858720 + TCGA-AG-3742-01 COSM1560924 c.1554C>A p.V518V Substitution - coding silent 10:120873921-120873921 + TCGA-AP-A051-01 COSM915452 c.337G>A p.A113T Substitution - Missense 10:120858781-120858781 + TCGA-B5-A11E-01 COSM915463 c.2483C>T p.A828V Substitution - Missense 10:120890855-120890855 + TCGA-AG-3892-01 COSM258361 c.2297T>G p.L766* Substitution - Nonsense 10:120889963-120889963 + TCGA-AP-A0LE-01 COSM915460 c.2024C>T p.A675V Substitution - Missense 10:120886739-120886739 + TCGA-76-6662-01 COSM3396949 c.2289T>C p.N763N Substitution - coding silent 10:120889955-120889955 + CSCC-40-T COSM4517022 c.2661_2662CC>TT p.Q888* Substitution - Nonsense 10:120901072-120901073 + BD177T COSM5517412 c.2644G>A p.E882K Substitution - Missense 10:120901055-120901055 + TCGA-EE-A3JA-06 COSM3434699 c.709C>T p.P237S Substitution - Missense 10:120862917-120862917 + 18195 COSM465354 c.823G>C p.V275L Substitution - Missense 10:120865156-120865156 + TCGA-22-5473-01 COSM683060 c.3194-1G>A p.? Unknown 10:120905318-120905318 + TCGA-BS-A0UF-01 COSM258361 c.2297T>G p.L766* Substitution - Nonsense 10:120889963-120889963 + sysucc-1370T COSM5469361 c.2570C>T p.A857V Substitution - Missense 10:120900083-120900083 + LUAD-S01356 COSM404420 c.1372G>C p.G458R Substitution - Missense 10:120871247-120871247 + HCC2998 COSM1675614 c.609A>G p.I203M Substitution - Missense 10:120862817-120862817 + L12 COSM5369062 c.1569G>A p.W523* Substitution - Nonsense 10:120878365-120878365 + STC263 COSM5049944 c.2924A>G p.Y975C Substitution - Missense 10:120903225-120903225 + PCSI_0007_Pa_X COSM3751573 c.2958G>A p.L986L Substitution - coding silent 10:120904073-120904073 + ESOSCC162T COSM1171666 c.1634A>T p.N545I Substitution - Missense 10:120878430-120878430 + RK050_C01 COSM1627346 c.212G>A p.R71K Substitution - Missense 10:120858656-120858656 + TCGA-43-3920-01 COSM683058 c.3499G>T p.E1167* Substitution - Nonsense 10:120906837-120906837 + TCGA-ER-A19N-06 COSM1703157 c.3382C>T p.L1128F Substitution - Missense 10:120905966-120905966 + OSCC-GB_01110111 COSM2056066 c.3197G>A p.G1066D Substitution - Missense 10:120905322-120905322 + QC2-26-T2 COSM3751573 c.2958G>A p.L986L Substitution - coding silent 10:120904073-120904073 + TCGA-28-5211-01 COSM3747851 c.585A>G p.S195S Substitution - coding silent 10:120862793-120862793 + SC_9047 COSM5573373 c.87-1G>T p.? Unknown 10:120852523-120852523 + sysucc-882T COSM5446844 c.2751A>G p.S917S Substitution - coding silent 10:120902320-120902320 + TCGA-EE-A183-06 COSM3434700 c.869C>T p.P290L Substitution - Missense 10:120865202-120865202 + cSCCP4 COSM138787 c.8C>T p.P3L Substitution - Missense 10:120851428-120851428 + HCC084T COSM5822327 c.2498A>G p.D833G Substitution - Missense 10:120890870-120890870 + TCGA-22-5473-01 COSM683062 c.295G>C p.D99H Substitution - Missense 10:120858739-120858739 + A9 COSM5349540 c.2211G>C p.L737F Substitution - Missense 10:120889167-120889167 + TCGA-D1-A16Y-01 COSM915456 c.1411C>T p.R471C Substitution - Missense 10:120871286-120871286 + RK067_C01 COSM1627347 c.797G>C p.R266P Substitution - Missense 10:120865130-120865130 + T3724 COSM4740841 c.243A>G p.P81P Substitution - coding silent 10:120858687-120858687 + SM-4B296 COSM4411569 c.1A>T p.M1L Substitution - Missense 10:120851421-120851421 + TCGA-BR-8078-01 COSM4012139 c.2663A>G p.Q888R Substitution - Missense 10:120901074-120901074 + TCGA-AD-6901-01 COSM1346172 c.958T>C p.Y320H Substitution - Missense 10:120865708-120865708 + Gp5D COSM2056007 c.132A>T p.V44V Substitution - coding silent 10:120852569-120852569 + LC_S6 COSM1190831 c.1574delG p.S525fs*2 Deletion - Frameshift 10:120878370-120878370 + TCGA-EE-A29N-06 COSM915456 c.1411C>T p.R471C Substitution - Missense 10:120871286-120871286 + Gp2D COSM2056007 c.132A>T p.V44V Substitution - coding silent 10:120852569-120852569 + 400 COSM4429349 c.1024G>C p.D342H Substitution - Missense 10:120866598-120866598 + HCC156T COSM3665547 c.1191-8C>A p.? Unknown 10:120867058-120867058 + TCGA-FK-A3SG-01 COSM3367923 c.416A>G p.N139S Substitution - Missense 10:120860172-120860172 + TCGA-HJ-7597-01 COSM1346177 c.2731C>T p.Q911* Substitution - Nonsense 10:120902300-120902300 + TCGA-KK-A6E4-01 COSM4876451 c.2767G>T p.E923* Substitution - Nonsense 10:120903068-120903068 + TCGA-DK-A3X1-01 COSM3790526 c.705G>A p.E235E Substitution - coding silent 10:120862913-120862913 + 1_RESISTANT COSM1720978 c.343C>T p.P115S Substitution - Missense 10:120858787-120858787 + HCC161T COSM3665546 c.6G>A p.L2L Substitution - coding silent 10:120851426-120851426 + ZZUFHECRKL-G051T COSM5431189 c.3235G>A p.A1079T Substitution - Missense 10:120905360-120905360 + PT23_1 COSM5902961 c.3028-8C>T p.? Unknown 10:120904638-120904638 + TCGA-16-1045-01 COSM3396948 c.1868A>G p.N623S Substitution - Missense 10:120885833-120885833 + HCC042T COSM5823689 c.1982A>T p.Q661L Substitution - Missense 10:120886697-120886697 + T3262 COSM4740842 c.1662A>G p.T554T Substitution - coding silent 10:120878458-120878458 + TCGA-AG-A002-01 COSM264682 c.2148C>T p.I716I Substitution - coding silent 10:120889104-120889104 + TCGA-B5-A11N-01 COSM915465 c.3592C>T p.L1198F Substitution - Missense 10:120908630-120908630 + Pat_26_B COSM5836361 c.1094C>T p.P365L Substitution - Missense 10:120866668-120866668 + CHC1750T COSM4792635 c.3272G>C p.R1091P Substitution - Missense 10:120905397-120905397 + CPCG0103-P4 COSM3395959 c.1945C>A p.L649M Substitution - Missense 10:120885910-120885910 + TCGA-FS-A4F5-06 COSM3434701 c.930T>C p.G310G Substitution - coding silent 10:120865680-120865680 + LIM2551 COSM4643437 c.2808G>A p.L936L Substitution - coding silent 10:120903109-120903109 + 19M COSM5579978 c.862G>A p.G288R Substitution - Missense 10:120865195-120865195 + I2L-P19Ta-Tumor-Organoid COSM5359950 c.2754-2A>G p.? Unknown 10:120903053-120903053 + TCGA-CJ-4882-01 COSM465356 c.2716G>T p.E906* Substitution - Nonsense 10:120902285-120902285 + TCGA-AA-3672-01 COSM267757 c.2266C>T p.R756C Substitution - Missense 10:120889932-120889932 + OSCC-GB_01020111 COSM1703157 c.3382C>T p.L1128F Substitution - Missense 10:120905966-120905966 + sysucc-880T COSM5461813 c.2553C>A p.A851A Substitution - coding silent 10:120900066-120900066 + TCGA-BR-7851-01 COSM4012137 c.1030C>T p.R344* Substitution - Nonsense 10:120866604-120866604 + TCGA-23-2645-01 COSM271603 c.3203A>G p.Q1068R Substitution - Missense 10:120905328-120905328 + TCGA-AM-5820-01 COSM3751573 c.2958G>A p.L986L Substitution - coding silent 10:120904073-120904073 + PCSI_0294_Pa_P_526 COSM380817 c.1328G>A p.R443K Substitution - Missense 10:120871203-120871203 + AOCS-153-1-2 COSM4422279 c.2821C>T p.Q941* Substitution - Nonsense 10:120903122-120903122 + 587290 COSM1232547 c.89G>A p.G30D Substitution - Missense 10:120852526-120852526 + TCGA-AA-3492-01 COSM1346176 c.2422A>G p.K808E Substitution - Missense 10:120890794-120890794 + pfg017T COSM1638461 c.714-9delT p.? Unknown 10:120865038-120865038 + DN1401F COSM5960888 c.3363C>A p.V1121V Substitution - coding silent 10:120905947-120905947 + TCGA-A6-6653-01 COSM1346174 c.1770A>G p.K590K Substitution - coding silent 10:120883810-120883810 + RK182_C01 COSM1627348 c.1634A>G p.N545S Substitution - Missense 10:120878430-120878430 + TCGA-GC-A3I6-01 COSM1297000 c.2123G>A p.G708E Substitution - Missense 10:120889079-120889079 + TCGA-CJ-5679-01 COSM465354 c.823G>C p.V275L Substitution - Missense 10:120865156-120865156 + sysucc-1163T COSM5458103 c.1125G>A p.V375V Substitution - coding silent 10:120866699-120866699 + HCC156 COSM3665547 c.1191-8C>A p.? Unknown 10:120867058-120867058 + LUAD-NYU1051S COSM368502 c.1526A>T p.K509I Substitution - Missense 10:120873893-120873893 + HCC112T COSM5818601 c.778A>T p.M260L Substitution - Missense 10:120865111-120865111 + Pat_02_B COSM5836362 c.1111G>A p.A371T Substitution - Missense 10:120866685-120866685 + 39 COSM4777706 c.590_591insC p.G198fs*12 Insertion - Frameshift 10:120862798-120862799 + 1293T COSM5763022 c.2039T>A p.V680E Substitution - Missense 10:120886754-120886754 + TCGA-D3-A2J8-06 COSM3434698 c.191T>C p.V64A Substitution - Missense 10:120852628-120852628 + CSCC-45-T COSM4459277 c.1119C>T p.L373L Substitution - coding silent 10:120866693-120866693 + HCC161 COSM3665546 c.6G>A p.L2L Substitution - coding silent 10:120851426-120851426 + TCGA-B0-5075-01 COSM465357 c.2999G>A p.C1000Y Substitution - Missense 10:120904114-120904114 + MD-274 COSM303562 c.1066G>A p.V356I Substitution - Missense 10:120866640-120866640 + YUROC COSM5370154 c.2761G>A p.G921S Substitution - Missense 10:120903062-120903062 + TCGA-AX-A0J0-01 COSM915458 c.1713C>T p.I571I Substitution - coding silent 10:120880875-120880875 + PT55 COSM4174676 c.1003C>T p.P335S Substitution - Missense 10:120866577-120866577 + Pat_66_A COSM5836366 c.2503C>A p.Q835K Substitution - Missense 10:120890875-120890875 + TCGA-A2-A0T0-01 COSM427152 c.1997_2007del11 p.L669fs*13 Deletion - Frameshift 10:120886712-120886722 + 0038_CRUK_PC_0038_T1_DNA COSM3434703 c.3384C>T p.L1128L Substitution - coding silent 10:120905968-120905968 + HCC2998 COSM1675614 c.609A>G p.I203M Substitution - Missense 10:120862817-120862817 + 990396 COSM1582051 c.1393G>A p.A465T Substitution - Missense 10:120871268-120871268 + TCGA-E2-A1IN-01 COSM1474406 c.686A>G p.K229R Substitution - Missense 10:120862894-120862894 + PTC-7C COSM3751573 c.2958G>A p.L986L Substitution - coding silent 10:120904073-120904073 + HCC2998 COSM286499 c.2430C>A p.I810I Substitution - coding silent 10:120890802-120890802 + TCGA-D1-A103-01 COSM915464 c.3331C>T p.R1111W Substitution - Missense 10:120905915-120905915 + HCC174T COSM3746202 c.1442T>A p.I481N Substitution - Missense 10:120871317-120871317 + 2492703 COSM5600852 c.3391C>T p.L1131F Substitution - Missense 10:120905975-120905975 + 3N34-VS-3T34 COSM4980941 c.1301G>T p.S434I Substitution - Missense 10:120871176-120871176 + TCGA-FG-5965-01 COSM3966913 c.3088G>C p.D1030H Substitution - Missense 10:120904706-120904706 + 166 COSM3724163 c.552C>T p.F184F Substitution - coding silent 10:120862760-120862760 + PD22357a COSM5784070 c.2519C>T p.P840L Substitution - Missense 10:120900032-120900032 + TCGA-AG-A002-01 COSM264683 c.3661C>T p.P1221S Substitution - Missense 10:120908699-120908699 + TCGA-22-4613-01 COSM683061 c.2561C>A p.A854D Substitution - Missense 10:120900074-120900074 + 12-P8001 COSM4573416 c.2932A>C p.K978Q Substitution - Missense 10:120904047-120904047 + CRC-33T COSM5479490 c.1472-2A>T p.? Unknown 10:120873837-120873837 + Pat_28_B COSM5836363 c.1325C>T p.P442L Substitution - Missense 10:120871200-120871200 + CSCC-15-T COSM4516330 c.1803_1804CC>TT p.L602F Substitution - Missense 10:120883843-120883844 + TCGA-AP-A0LM-01 COSM915462 c.2414C>T p.T805M Substitution - Missense 10:120890786-120890786 + TCGA-AA-A010-01 COSM286499 c.2430C>A p.I810I Substitution - coding silent 10:120890802-120890802 + PCSI_0083_Pa_X COSM2056015 c.898C>T p.R300C Substitution - Missense 10:120865648-120865648 + 2492700 COSM5600852 c.3391C>T p.L1131F Substitution - Missense 10:120905975-120905975 + RMH004-R4 COSM4411235 c.1783T>A p.W595R Substitution - Missense 10:120883823-120883823 + TCGA-BS-A0UF-01 COSM915455 c.603T>G p.V201V Substitution - coding silent 10:120862811-120862811 + BD49T COSM5497989 c.485T>A p.L162H Substitution - Missense 10:120860241-120860241 + RMH004-VT COSM4411235 c.1783T>A p.W595R Substitution - Missense 10:120883823-120883823 + tumor_4159170 COSM1160949 c.759G>A p.L253L Substitution - coding silent 10:120865092-120865092 + 1_PRE-TREATMENT COSM1720978 c.343C>T p.P115S Substitution - Missense 10:120858787-120858787 + T1154 COSM4740840 c.40A>G p.T14A Substitution - Missense 10:120851460-120851460 + RMH004-R10 COSM4411235 c.1783T>A p.W595R Substitution - Missense 10:120883823-120883823 + ESO-864 COSM1270368 c.3429G>A p.T1143T Substitution - coding silent 10:120906013-120906013 + T3058 COSM1270368 c.3429G>A p.T1143T Substitution - coding silent 10:120906013-120906013 + 49M COSM5593963 c.339C>T p.A113A Substitution - coding silent 10:120858783-120858783 + CHC2112T COSM4956761 c.836T>C p.V279A Substitution - Missense 10:120865169-120865169 + BD114T COSM5503668 c.3379G>A p.A1127T Substitution - Missense 10:120905963-120905963 + TCGA-HE-A5NF-01 COSM3985461 c.3028-1G>A p.? Unknown 10:120904645-120904645 + GC8_T COSM147069 c.3363C>G p.V1121V Substitution - coding silent 10:120905947-120905947 + TCGA-AU-6004-01 COSM1346180 c.3318C>T p.A1106A Substitution - coding silent 10:120905902-120905902 + LAU63 COSM234453 c.360G>A p.Q120Q Substitution - coding silent 10:120860116-120860116 + I2L-P19Ta-Tumor-Biopsy COSM5359950 c.2754-2A>G p.? Unknown 10:120903053-120903053 + PCSI_0083_Pa_P_526 COSM2056015 c.898C>T p.R300C Substitution - Missense 10:120865648-120865648 + ESO-0292 COSM1241894 c.703G>C p.E235Q Substitution - Missense 10:120862911-120862911 + YUKAT COSM5370153 c.2430C>T p.I810I Substitution - coding silent 10:120890802-120890802 + CSCC-47-T COSM4511978 c.887C>T p.P296L Substitution - Missense 10:120865637-120865637 + GC8_T COSM147067 c.1899A>T p.A633A Substitution - coding silent 10:120885864-120885864 + PT23_1 COSM5902962 c.3028-7T>C p.? Unknown 10:120904639-120904639 + S00932 COSM309539 c.1282G>A p.D428N Substitution - Missense 10:120867157-120867157 + Au2 COSM5600852 c.3391C>T p.L1131F Substitution - Missense 10:120905975-120905975 + S00932 COSM309539 c.1282G>A p.D428N Substitution - Missense 10:120867157-120867157 + 2492701 COSM5600852 c.3391C>T p.L1131F Substitution - Missense 10:120905975-120905975 + 053T COSM1729906 c.1146A>G p.I382M Substitution - Missense 10:120866720-120866720 + TCGA-CM-6162-01 COSM1346173 c.1681C>T p.R561C Substitution - Missense 10:120880843-120880843 + TCGA-D1-A167-01 COSM915453 c.387C>T p.R129R Substitution - coding silent 10:120860143-120860143 + pfg181T COSM4760822 c.25A>G p.K9E Substitution - Missense 10:120851445-120851445 + TCGA-A8-A092-01 COSM427153 c.2252G>C p.W751S Substitution - Missense 10:120889918-120889918 + CHC469T COSM3666664 c.683T>C p.V228A Substitution - Missense 10:120862891-120862891 + TCGA-AA-A010-01 COSM286498 c.1827C>T p.N609N Substitution - coding silent 10:120883867-120883867 + WA47 COSM242242 c.439G>A p.D147N Substitution - Missense 10:120860195-120860195 + TCGA-D5-5538-01 COSM1346178 c.2931+1G>T p.? Unknown 10:120903233-120903233 + sysucc-825T COSM5485201 c.3182G>T p.G1061V Substitution - Missense 10:120904800-120904800 + TCGA-43-3920-01 COSM683059 c.3472G>A p.E1158K Substitution - Missense 10:120906810-120906810 + SNUH_G76_S1 COSM4419715 c.3393C>T p.L1131L Substitution - coding silent 10:120905977-120905977 + RMH004-R3 COSM4411235 c.1783T>A p.W595R Substitution - Missense 10:120883823-120883823 + T3255 COSM4740843 c.2095A>T p.K699* Substitution - Nonsense 10:120886810-120886810 + 255 COSM3732443 c.3292-1G>T p.? Unknown 10:120905875-120905875 + ESCC_118 COSM5640142 c.1776G>A p.L592L Substitution - coding silent 10:120883816-120883816 + TCGA-A8-A0A6-01 COSM3806590 c.2160T>G p.G720G Substitution - coding silent 10:120889116-120889116 + TCGA-FD-A3SJ-01 COSM3790527 c.1174C>A p.R392R Substitution - coding silent 10:120866748-120866748 + TCGA-F4-6856-01 COSM1346175 c.2232A>G p.G744G Substitution - coding silent 10:120889898-120889898 + TCGA-E5-A2PC-01 COSM465354 c.823G>C p.V275L Substitution - Missense 10:120865156-120865156 + ESCC_77 COSM5635305 c.614G>A p.S205N Substitution - Missense 10:120862822-120862822 + HCC006T COSM5803419 c.1475C>T p.T492I Substitution - Missense 10:120873842-120873842 + RK050_C COSM1627346 c.212G>A p.R71K Substitution - Missense 10:120858656-120858656 + CHC2112T COSM4956761 c.836T>C p.V279A Substitution - Missense 10:120865169-120865169 + TCGA-UC-A7PF-01 COSM4830228 c.3125C>T p.S1042L Substitution - Missense 10:120904743-120904743 + TCGA-A3-3362-01 COSM465355 c.1198G>T p.G400C Substitution - Missense 10:120867073-120867073 + 8015259 COSM3382701 c.156A>C p.Q52H Substitution - Missense 10:120852593-120852593 + CSCC-40-T COSM4469581 c.1607C>T p.T536I Substitution - Missense 10:120878403-120878403 + CHC1750T COSM4792635 c.3272G>C p.R1091P Substitution - Missense 10:120905397-120905397 + YUAKER COSM1703157 c.3382C>T p.L1128F Substitution - Missense 10:120905966-120905966 + TCGA-EW-A1IZ-01 COSM1474407 c.1837A>G p.I613V Substitution - Missense 10:120883877-120883877 + TCGA-HU-A4H4-01 COSM4012135 c.755A>G p.Y252C Substitution - Missense 10:120865088-120865088 + CMPC11-3104 COSM2056064 c.3096G>A p.L1032L Substitution - coding silent 10:120904714-120904714 + GC_353T-GC_353N COSM4773472 c.3181G>A p.G1061S Substitution - Missense 10:120904799-120904799 + GC8_T COSM147066 c.834G>A p.T278T Substitution - coding silent 10:120865167-120865167 + NCI-H835 COSM2056022 c.1079G>C p.S360T Substitution - Missense 10:120866653-120866653 + 2492702 COSM5600852 c.3391C>T p.L1131F Substitution - Missense 10:120905975-120905975 + CHC976T COSM3666665 c.1553T>G p.V518G Substitution - Missense 10:120873920-120873920 + TCGA-G4-6588-01 COSM1346177 c.2731C>T p.Q911* Substitution - Nonsense 10:120902300-120902300 + LUAD-RT-S01769 COSM380817 c.1328G>A p.R443K Substitution - Missense 10:120871203-120871203 + TCGA-EE-A2MR-06 COSM3434702 c.3132C>T p.G1044G Substitution - coding silent 10:120904750-120904750 + ccRCC-22 COSM1664984 c.1794G>T p.R598S Substitution - Missense 10:120883834-120883834 + SW48 COSM2056045 c.2331G>T p.W777C Substitution - Missense 10:120889997-120889997 + CSCC-5-T COSM4540364 c.282G>C p.K94N Substitution - Missense 10:120858726-120858726 + TCGA-D5-6540-01 COSM915464 c.3331C>T p.R1111W Substitution - Missense 10:120905915-120905915 + S02397 COSM5699010 c.3658G>A p.E1220K Substitution - Missense 10:120908696-120908696 + 855_PT COSM5753419 c.1298A>G p.Q433R Substitution - Missense 10:120871173-120871173 + TARGET-30-PASCKI COSM1288929 c.1291A>T p.I431F Substitution - Missense 10:120867166-120867166 + SNU-C2B COSM2056047 c.2390G>A p.R797H Substitution - Missense 10:120890762-120890762 + TCGA-BQ-5890-01 COSM3985462 c.3343C>A p.H1115N Substitution - Missense 10:120905927-120905927 + GC8_T COSM147065 c.199-7G>C p.? Unknown 10:120858636-120858636 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.144447 10q26 606417 2466909|CGAP|BC040469|G/T|non-coding||4237|Candidate; 2466909|CGAP|BC071564|G/T|non-coding||4199|Candidate; 1515106|dbSNP|BC040469|G/T|non-coding||4298|Validated; 1515106|dbSNP|BC071564|G/T|non-coding||4260|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AATCTGAACTT - Frameshift p.L669Hfs*13 c.1998_2008delATCTGAACTTA 10 122646224 BRCA AGAA - Frameshift p.E664Vfs*34 c.1991_1994delAAAG 10 122646216 PRAD A G Missense p.K229R c.686A>G 10 122622406 BRCA A G Missense p.N139S c.416A>G 10 122619684 THCA A G Missense p.N623S c.1868A>G 10 122645345 GBM A G Missense p.N92S c.275A>G 10 122618231 BRCA A G Synonymous p.S195S c.585A>G 10 122622305 GBM A T Missense p.I431F c.1291A>T 10 122626678 NB A T Synonymous p.A435A c.1305A>T 10 122630692 LUAD C A IntronicSNV . c.3437+48C>A 10 122665581 CM C A Missense p.A854D c.2561C>A 10 122659586 LUSC C A Missense p.S165Y c.494C>A 10 122619762 UCEC C T IntronicSNV . c.3437+50C>T 10 122665583 HC C T Missense p.A675V c.2024C>T 10 122646251 UCEC C T Missense p.L1128F c.3382C>T 10 122665478 CM C T Missense p.P237S c.709C>T 10 122622429 CM C T Missense p.P290L c.869C>T 10 122624714 CM C T Missense p.R129C c.385C>T 10 122619653 HNSC C T Missense p.R471C c.1411C>T 10 122630798 CM C T Missense p.R471C c.1411C>T 10 122630798 UCEC C T Missense p.R797C c.2389C>T 10 122650273 CM C T Missense p.S195L c.584C>T 10 122622304 LUAD C T Synonymous p.F184F c.552C>T 10 122622272 HNSC C T Synonymous p.F241F c.723C>T 10 122624568 CM C T Synonymous p.L1128L c.3384C>T 10 122665480 CM C T Synonymous p.L143L c.429C>T 10 122619697 CM G A Missense p.C1000Y c.2999G>A 10 122663626 RCCC G A Missense p.D428N c.1282G>A 10 122626669 SCLC G A Missense p.E108K c.322G>A 10 122618278 HNSC G A Missense p.E1158K c.3472G>A 10 122666322 LUSC G A Missense p.G708E c.2123G>A 10 122648591 BLCA G A Missense p.G720S c.2158G>A 10 122648626 CM G A Missense p.R315H c.944G>A 10 122625206 STAD G A Missense p.R71K c.212G>A 10 122618168 HC G A Nonsense p.W29* c.87G>A 10 122612036 HNSC G A Nonsense p.W31* c.92G>A 10 122612041 STAD G A SpliceAcceptorSNV . c.3194-1G>A 10 122664830 LUSC G A Synonymous p.K1188K c.3564G>A 10 122668114 HNSC G A Synonymous p.L253L c.759G>A 10 122624604 DLBCL G A Synonymous p.T1143T c.3429G>A 10 122665525 ESCA G C Missense p.D1030H c.3088G>C 10 122664218 LGG G C Missense p.D99H c.295G>C 10 122618251 LUSC G C Missense p.K155N c.465G>C 10 122619733 BLCA G C Missense p.R266P c.797G>C 10 122624642 HC G C Missense p.V275L c.823G>C 10 122624668 BLCA G C Missense p.V275L c.823G>C 10 122624668 RCCC G C Missense p.W751S c.2252G>C 10 122649430 BRCA GG AA SpliceAcceptorBlockSubstitution . c.3292-1_3292delinsAA 10 122665387 CM G T Missense p.R286L c.857G>T 10 122624702 HNSC G T Missense p.V586L c.1756G>T 10 122643308 LUAD G T Nonsense p.E1167* c.3499G>T 10 122666349 LUSC G T Nonsense p.E906* c.2716G>T 10 122661797 RCCC G T Nonsense p.E923* c.2767G>T 10 122662580 PRAD T C IntronicSNV . c.1472-937T>C 10 122632414 CLL T C Missense p.L1161P c.3482T>C 10 122666332 CM T C Missense p.V64A c.191T>C 10 122612140 CM T C Synonymous p.N763N c.2289T>C 10 122649467 GBM T - IntronicDeletion . c.714-4delT 10 122624550 STAD