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 5948345 5948345 + Missense_Mutation SNP A A G TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr10:5948345A>G c.503A>G c.(502-504)gAc>gGc p.D168G ACC 10 5979171 5979172 + Frame_Shift_Del DEL GC GC - TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr10:5979171_5979172delGC c.3060_3061delGC c.(3058-3063)gtgcgcfs p.R1021fs BLCA 10 5945065 5945065 + Missense_Mutation SNP C C A TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr10:5945065C>A c.84C>A c.(82-84)ttC>ttA p.F28L BLCA 10 5945104 5945104 + Silent SNP C C T TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr10:5945104C>T c.123C>T c.(121-123)ctC>ctT p.L41L BLCA 10 5948587 5948587 + Missense_Mutation SNP G G A TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr10:5948587G>A c.745G>A c.(745-747)Gac>Aac p.D249N BLCA 10 5951128 5951128 + Silent SNP A A G TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr10:5951128A>G c.891A>G c.(889-891)acA>acG p.T297T BLCA 10 5951204 5951204 + Missense_Mutation SNP G G A TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr10:5951204G>A c.967G>A c.(967-969)Gag>Aag p.E323K BLCA 10 5951259 5951259 + Splice_Site DEL T T - TCGA-DK-AA6R-01A-11D-A42E-08 TCGA-DK-AA6R-10A-01D-A42H-08 g.chr10:5951259delT c.e5+2 BLCA 10 5952975 5952975 + Silent SNP C C G TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr10:5952975C>G c.1095C>G c.(1093-1095)ctC>ctG p.L365L BLCA 10 5955750 5955750 + Missense_Mutation SNP A A T TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr10:5955750A>T c.1252A>T c.(1252-1254)Aat>Tat p.N418Y BLCA 10 5958227 5958227 + Silent SNP C C T TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr10:5958227C>T c.1596C>T c.(1594-1596)ttC>ttT p.F532F BLCA 10 5959443 5959443 + Missense_Mutation SNP G G C TCGA-DK-A2I1-01A-11D-A17V-08 TCGA-DK-A2I1-10A-01D-A17V-08 g.chr10:5959443G>C c.1849G>C c.(1849-1851)Gaa>Caa p.E617Q BLCA 10 5959560 5959560 + Silent SNP G G A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr10:5959560G>A c.1884G>A c.(1882-1884)ttG>ttA p.L628L BLCA 10 5963400 5963416 + Splice_Site DEL TCTCCCTAAAGGTGGCA TCTCCCTAAAGGTGGCA - TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chr10:5963400_5963416delTCTCCCTAAAGGTGGCA c.2200_2206delTCTCCCTAAAGGTGGCA c.(2200-2208)tctccctaa>aa p.SP*734fs BLCA 10 5979159 5979159 + Silent SNP C C T TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr10:5979159C>T c.3048C>T c.(3046-3048)tcC>tcT p.S1016S BRCA 10 5937117 5937117 + Intron SNP G G T TCGA-B6-A0X7-01A-11D-A10M-09 TCGA-B6-A0X7-10A-01D-A10M-09 g.chr10:5937117G>T BRCA 10 5945053 5945053 + Silent SNP G G A TCGA-BH-A0C1-01B-11D-A12B-09 TCGA-BH-A0C1-10A-01D-A12B-09 g.chr10:5945053G>A c.72G>A c.(70-72)gtG>gtA p.V24V BRCA 10 5945069 5945069 + Nonsense_Mutation SNP C C T TCGA-A8-A0A9-01A-11W-A019-09 TCGA-A8-A0A9-10A-01W-A021-09 g.chr10:5945069C>T c.88C>T c.(88-90)Caa>Taa p.Q30* BRCA 10 5945078 5945081 + Frame_Shift_Del DEL ACAA ACAA - TCGA-LL-A441-01A-11D-A243-09 TCGA-LL-A441-10A-01D-A243-09 g.chr10:5945078_5945081delACAA c.97_100delACAA c.(97-102)acaaacfs p.TN33fs BRCA 10 5948163 5948163 + Frame_Shift_Del DEL C C - TCGA-AN-A0FX-01A-11W-A050-09 TCGA-AN-A0FX-10A-01W-A055-09 g.chr10:5948163delC c.321delC c.(319-321)ggcfs p.G107fs BRCA 10 5948251 5948251 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr10:5948251A>C c.409A>C c.(409-411)Acc>Ccc p.T137P BRCA 10 5948419 5948419 + Missense_Mutation SNP C C G TCGA-E2-A1LG-01A-21D-A14K-09 TCGA-E2-A1LG-11A-42D-A14K-09 g.chr10:5948419C>G c.577C>G c.(577-579)Cct>Gct p.P193A BRCA 10 5951018 5951018 + Splice_Site SNP G G A TCGA-D8-A1Y3-01A-11D-A159-09 TCGA-D8-A1Y3-10A-01D-A159-09 g.chr10:5951018G>A c.884G>A c.(883-885)cGa>cAa p.R295Q BRCA 10 5951233 5951233 + Silent SNP C C A TCGA-AN-A0AR-01A-11W-A019-09 TCGA-AN-A0AR-10A-01W-A021-09 g.chr10:5951233C>A c.996C>A c.(994-996)ctC>ctA p.L332L BRCA 10 5963220 5963220 + Splice_Site SNP G G T TCGA-BH-A0HB-01A-11W-A071-09 TCGA-BH-A0HB-10A-01W-A071-09 g.chr10:5963220G>T c.e14-1 BRCA 10 5969465 5969465 + Missense_Mutation SNP C C G TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr10:5969465C>G c.2790C>G c.(2788-2790)atC>atG p.I930M CESC 10 5945069 5945069 + Nonsense_Mutation SNP C C T TCGA-EK-A2RO-01A-11D-A18J-09 TCGA-EK-A2RO-10A-01D-A18J-09 g.chr10:5945069C>T c.88C>T c.(88-90)Caa>Taa p.Q30* CESC 10 5957376 5957376 + Silent SNP G G A TCGA-HG-A2PA-01A-11D-A20U-09 TCGA-HG-A2PA-10B-01D-A20U-09 g.chr10:5957376G>A c.1407G>A c.(1405-1407)aaG>aaA p.K469K CESC 10 5963484 5963484 + Silent SNP C C T TCGA-EK-A3GM-01A-11D-A20U-09 TCGA-EK-A3GM-10A-01D-A20U-09 g.chr10:5963484C>T c.2274C>T c.(2272-2274)gcC>gcT p.A758A COAD 10 5937117 5937117 + Intron SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr10:5937117G>A COAD 10 5937144 5937144 + Intron DEL G G - TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr10:5937144delG COAD 10 5948209 5948209 + Missense_Mutation SNP C C T TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chr10:5948209C>T c.367C>T c.(367-369)Cgg>Tgg p.R123W COAD 10 5948356 5948356 + Missense_Mutation SNP C C T TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr10:5948356C>T c.514C>T c.(514-516)Cgg>Tgg p.R172W COAD 10 5948409 5948409 + Silent SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr10:5948409T>C c.567T>C c.(565-567)ccT>ccC p.P189P COAD 10 5948498 5948498 + Missense_Mutation SNP T T A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr10:5948498T>A c.656T>A c.(655-657)gTc>gAc p.V219D COAD 10 5951235 5951235 + Missense_Mutation SNP C C T TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr10:5951235C>T c.998C>T c.(997-999)cCc>cTc p.P333L COAD 10 5952926 5952926 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:5952926C>T c.1046C>T c.(1045-1047)gCg>gTg p.A349V COAD 10 5956157 5956157 + Missense_Mutation SNP C C G TCGA-AA-3666-01A-02W-0900-09 TCGA-AA-3666-10A-01W-0900-09 g.chr10:5956157C>G c.1321C>G c.(1321-1323)Ctt>Gtt p.L441V COAD 10 5957384 5957384 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr10:5957384C>T c.1415C>T c.(1414-1416)aCg>aTg p.T472M COAD 10 5959402 5959402 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:5959402G>A c.1808G>A c.(1807-1809)aGc>aAc p.S603N COAD 10 5959451 5959451 + Silent SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:5959451G>A c.1857G>A c.(1855-1857)gcG>gcA p.A619A COAD 10 5959615 5959615 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr10:5959615G>A c.1939G>A c.(1939-1941)Gat>Aat p.D647N COAD 10 5960396 5960396 + Silent SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr10:5960396C>T c.2055C>T c.(2053-2055)aaC>aaT p.N685N COAD 10 5963427 5963427 + Silent SNP C C T TCGA-AA-3939-01A-01W-0995-10 TCGA-AA-3939-10A-01W-0995-10 g.chr10:5963427C>T c.2217C>T c.(2215-2217)gaC>gaT p.D739D COAD 10 5963484 5963484 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr10:5963484C>T c.2274C>T c.(2272-2274)gcC>gcT p.A758A COAD 10 5965614 5965614 + Missense_Mutation SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr10:5965614A>G c.2353A>G c.(2353-2355)Att>Gtt p.I785V COAD 10 5965659 5965659 + Splice_Site SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr10:5965659C>T c.2398C>T c.(2398-2400)Caa>Taa p.Q800* COAD 10 5969473 5969473 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:5969473A>C c.2798A>C c.(2797-2799)aAa>aCa p.K933T COAD 10 5978482 5978482 + Missense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr10:5978482G>A c.2893G>A c.(2893-2895)Gtg>Atg p.V965M COAD 10 5978484 5978484 + Silent SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr10:5978484G>A c.2895G>A c.(2893-2895)gtG>gtA p.V965V COAD 10 5978510 5978510 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:5978510T>C c.2921T>C c.(2920-2922)gTt>gCt p.V974A COAD 10 5979158 5979158 + Frame_Shift_Del DEL C C - TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:5979158delC c.3047delC c.(3046-3048)tccfs p.S1016fs COADREAD 10 5937117 5937117 + Intron SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr10:5937117G>A COADREAD 10 5937144 5937144 + Intron DEL G G - TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr10:5937144delG COADREAD 10 5948209 5948209 + Missense_Mutation SNP C C T TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chr10:5948209C>T c.367C>T c.(367-369)Cgg>Tgg p.R123W COADREAD 10 5948356 5948356 + Missense_Mutation SNP C C T TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr10:5948356C>T c.514C>T c.(514-516)Cgg>Tgg p.R172W COADREAD 10 5948409 5948409 + Silent SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr10:5948409T>C c.567T>C c.(565-567)ccT>ccC p.P189P COADREAD 10 5948498 5948498 + Missense_Mutation SNP T T A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr10:5948498T>A c.656T>A c.(655-657)gTc>gAc p.V219D COADREAD 10 5951235 5951235 + Missense_Mutation SNP C C T TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr10:5951235C>T c.998C>T c.(997-999)cCc>cTc p.P333L COADREAD 10 5952926 5952926 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:5952926C>T c.1046C>T c.(1045-1047)gCg>gTg p.A349V COADREAD 10 5956157 5956157 + Missense_Mutation SNP C C G TCGA-AA-3666-01A-02W-0900-09 TCGA-AA-3666-10A-01W-0900-09 g.chr10:5956157C>G c.1321C>G c.(1321-1323)Ctt>Gtt p.L441V COADREAD 10 5957384 5957384 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr10:5957384C>T c.1415C>T c.(1414-1416)aCg>aTg p.T472M COADREAD 10 5959402 5959402 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:5959402G>A c.1808G>A c.(1807-1809)aGc>aAc p.S603N COADREAD 10 5959451 5959451 + Silent SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:5959451G>A c.1857G>A c.(1855-1857)gcG>gcA p.A619A COADREAD 10 5959615 5959615 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr10:5959615G>A c.1939G>A c.(1939-1941)Gat>Aat p.D647N COADREAD 10 5960396 5960396 + Silent SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr10:5960396C>T c.2055C>T c.(2053-2055)aaC>aaT p.N685N COADREAD 10 5963427 5963427 + Silent SNP C C T TCGA-AA-3939-01A-01W-0995-10 TCGA-AA-3939-10A-01W-0995-10 g.chr10:5963427C>T c.2217C>T c.(2215-2217)gaC>gaT p.D739D COADREAD 10 5963484 5963484 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr10:5963484C>T c.2274C>T c.(2272-2274)gcC>gcT p.A758A COADREAD 10 5965614 5965614 + Missense_Mutation SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr10:5965614A>G c.2353A>G c.(2353-2355)Att>Gtt p.I785V COADREAD 10 5965659 5965659 + Splice_Site SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr10:5965659C>T c.2398C>T c.(2398-2400)Caa>Taa p.Q800* COADREAD 10 5969473 5969473 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:5969473A>C c.2798A>C c.(2797-2799)aAa>aCa p.K933T COADREAD 10 5978482 5978482 + Missense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr10:5978482G>A c.2893G>A c.(2893-2895)Gtg>Atg p.V965M COADREAD 10 5978484 5978484 + Silent SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr10:5978484G>A c.2895G>A c.(2893-2895)gtG>gtA p.V965V COADREAD 10 5978510 5978510 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:5978510T>C c.2921T>C c.(2920-2922)gTt>gCt p.V974A COADREAD 10 5979158 5979158 + Frame_Shift_Del DEL C C - TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:5979158delC c.3047delC c.(3046-3048)tccfs p.S1016fs DLBC 10 5948352 5948352 + Silent SNP G G A TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr10:5948352G>A c.510G>A c.(508-510)acG>acA p.T170T DLBC 10 5960434 5960434 + Missense_Mutation SNP T T C TCGA-GR-A4D9-01B-11D-A31X-10 TCGA-GR-A4D9-10A-01D-A31X-10 g.chr10:5960434T>C c.2093T>C c.(2092-2094)cTc>cCc p.L698P ESCA 10 5955768 5955768 + Missense_Mutation SNP A A G TCGA-LN-A5U7-01A-11D-A31U-09 TCGA-LN-A5U7-10A-01D-A31U-09 g.chr10:5955768A>G c.1270A>G c.(1270-1272)Aca>Gca p.T424A ESCA 10 5957464 5957464 + Nonsense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr10:5957464G>T c.1495G>T c.(1495-1497)Gaa>Taa p.E499* ESCA 10 5960397 5960397 + Missense_Mutation SNP G G T TCGA-LN-A9FR-01A-11D-A387-09 TCGA-LN-A9FR-10A-01D-A38A-09 g.chr10:5960397G>T c.2056G>T c.(2056-2058)Gcc>Tcc p.A686S GBMLGG 10 5948527 5948527 + Missense_Mutation SNP G G T TCGA-HT-7480-01A-11D-2086-08 TCGA-HT-7480-10A-01D-2086-08 g.chr10:5948527G>T c.685G>T c.(685-687)Gtg>Ttg p.V229L GBMLGG 10 5979128 5979128 + Missense_Mutation SNP G G A TCGA-HT-7692-01A-12D-2253-08 TCGA-HT-7692-10A-01D-2253-08 g.chr10:5979128G>A c.3017G>A c.(3016-3018)cGc>cAc p.R1006H HNSC 10 5948284 5948284 + Missense_Mutation SNP C C T TCGA-CV-6945-01A-11D-1912-08 TCGA-CV-6945-10A-01D-1912-08 g.chr10:5948284C>T c.442C>T c.(442-444)Cca>Tca p.P148S HNSC 10 5948405 5948405 + Missense_Mutation SNP G G A TCGA-CV-7415-01A-11D-2078-08 TCGA-CV-7415-10A-01D-2078-08 g.chr10:5948405G>A c.563G>A c.(562-564)gGt>gAt p.G188D HNSC 10 5948426 5948426 + Nonsense_Mutation SNP C C G TCGA-BB-A5HU-01A-11D-A28R-08 TCGA-BB-A5HU-10A-01D-A28U-08 g.chr10:5948426C>G c.584C>G c.(583-585)tCa>tGa p.S195* HNSC 10 5951018 5951018 + Splice_Site SNP G G A TCGA-CR-7390-01A-11D-2012-08 TCGA-CR-7390-10A-01D-2013-08 g.chr10:5951018G>A c.884G>A c.(883-885)cGa>cAa p.R295Q HNSC 10 5951148 5951148 + Missense_Mutation SNP C C T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr10:5951148C>T c.911C>T c.(910-912)cCg>cTg p.P304L HNSC 10 5951160 5951160 + Missense_Mutation SNP C C T TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr10:5951160C>T c.923C>T c.(922-924)cCc>cTc p.P308L HNSC 10 5951214 5951214 + Missense_Mutation SNP C C T TCGA-CV-7416-01A-11D-2078-08 TCGA-CV-7416-10A-01D-2078-08 g.chr10:5951214C>T c.977C>T c.(976-978)gCg>gTg p.A326V HNSC 10 5953002 5953002 + Silent SNP G G T TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr10:5953002G>T c.1122G>T c.(1120-1122)acG>acT p.T374T HNSC 10 5956205 5956205 + Nonsense_Mutation SNP C C T TCGA-CR-7368-01A-11D-2129-08 TCGA-CR-7368-10A-01D-2129-08 g.chr10:5956205C>T c.1369C>T c.(1369-1371)Cag>Tag p.Q457* HNSC 10 5958267 5958267 + Frame_Shift_Del DEL G G - TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr10:5958267delG c.1636delG c.(1636-1638)gggfs p.G546fs HNSC 10 5958323 5958323 + Silent SNP T T C TCGA-CV-7422-01A-21D-2078-08 TCGA-CV-7422-10A-01D-2078-08 g.chr10:5958323T>C c.1692T>C c.(1690-1692)ttT>ttC p.F564F HNSC 10 5958338 5958338 + Silent SNP A A G TCGA-CQ-A4CB-01A-11D-A25D-08 TCGA-CQ-A4CB-10A-01D-A25E-08 g.chr10:5958338A>G c.1707A>G c.(1705-1707)gaA>gaG p.E569E HNSC 10 5963255 5963255 + Missense_Mutation SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr10:5963255G>A c.2135G>A c.(2134-2136)gGa>gAa p.G712E HNSC 10 5966446 5966446 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr10:5966446C>T c.2571C>T c.(2569-2571)tgC>tgT p.C857C KICH 10 5960320 5960320 + Missense_Mutation SNP T T C TCGA-KN-8431-01A-11D-2310-10 TCGA-KN-8431-11A-01D-2311-10 g.chr10:5960320T>C c.1979T>C c.(1978-1980)gTt>gCt p.V660A KICH 10 5978506 5978506 + Missense_Mutation SNP C C T TCGA-KN-8426-01A-11D-2310-10 TCGA-KN-8426-11A-01D-2311-10 g.chr10:5978506C>T c.2917C>T c.(2917-2919)Cct>Tct p.P973S KIPAN 10 5937075 5937075 + Intron SNP G G T TCGA-BP-5199-01A-01D-1429-08 TCGA-BP-5199-11A-01D-1429-08 g.chr10:5937075G>T KIPAN 10 5948166 5948166 + Silent SNP T T C TCGA-B0-4823-01A-02D-1421-08 TCGA-B0-4823-11A-01D-1421-08 g.chr10:5948166T>C c.324T>C c.(322-324)agT>agC p.S108S KIPAN 10 5950982 5950982 + Frame_Shift_Del DEL A A - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr10:5950982delA c.848delA c.(847-849)gaafs p.E283fs KIPAN 10 5951142 5951142 + Missense_Mutation SNP G G A TCGA-B8-4148-01A-02D-1386-10 TCGA-B8-4148-10A-01D-1251-10 g.chr10:5951142G>A c.905G>A c.(904-906)tGc>tAc p.C302Y KIPAN 10 5953065 5953070 + In_Frame_Del DEL GGAGAA GGAGAA - TCGA-B0-5094-01A-01D-1421-08 TCGA-B0-5094-11A-01D-1421-08 g.chr10:5953065_5953070delGGAGAA c.1185_1190delGGAGAA c.(1183-1191)agggagaag>agg p.EK396del KIPAN 10 5960320 5960320 + Missense_Mutation SNP T T C TCGA-KN-8431-01A-11D-2310-10 TCGA-KN-8431-11A-01D-2311-10 g.chr10:5960320T>C c.1979T>C c.(1978-1980)gTt>gCt p.V660A KIPAN 10 5963284 5963284 + Missense_Mutation SNP G G A TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr10:5963284G>A c.2164G>A c.(2164-2166)Gtc>Atc p.V722I KIPAN 10 5967396 5967404 + In_Frame_Del DEL ATTTTGTGA ATTTTGTGA - TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr10:5967396_5967404delATTTTGTGA c.2663_2671delATTTTGTGA c.(2662-2673)gattttgtgaaa>gaa p.888_891DFVK>E KIPAN 10 5978506 5978506 + Missense_Mutation SNP C C T TCGA-KN-8426-01A-11D-2310-10 TCGA-KN-8426-11A-01D-2311-10 g.chr10:5978506C>T c.2917C>T c.(2917-2919)Cct>Tct p.P973S KIRC 10 5937075 5937075 + Intron SNP G G T TCGA-BP-5199-01A-01D-1429-08 TCGA-BP-5199-11A-01D-1429-08 g.chr10:5937075G>T KIRC 10 5948166 5948166 + Silent SNP T T C TCGA-B0-4823-01A-02D-1421-08 TCGA-B0-4823-11A-01D-1421-08 g.chr10:5948166T>C c.324T>C c.(322-324)agT>agC p.S108S KIRC 10 5950982 5950982 + Frame_Shift_Del DEL A A - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr10:5950982delA c.848delA c.(847-849)gaafs p.E283fs KIRC 10 5951142 5951142 + Missense_Mutation SNP G G A TCGA-B8-4148-01A-02D-1386-10 TCGA-B8-4148-10A-01D-1251-10 g.chr10:5951142G>A c.905G>A c.(904-906)tGc>tAc p.C302Y KIRC 10 5953065 5953070 + In_Frame_Del DEL GGAGAA GGAGAA - TCGA-B0-5094-01A-01D-1421-08 TCGA-B0-5094-11A-01D-1421-08 g.chr10:5953065_5953070delGGAGAA c.1185_1190delGGAGAA c.(1183-1191)agggagaag>agg p.EK396del KIRC 10 5963284 5963284 + Missense_Mutation SNP G G A TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr10:5963284G>A c.2164G>A c.(2164-2166)Gtc>Atc p.V722I KIRC 10 5967396 5967404 + In_Frame_Del DEL ATTTTGTGA ATTTTGTGA - TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr10:5967396_5967404delATTTTGTGA c.2663_2671delATTTTGTGA c.(2662-2673)gattttgtgaaa>gaa p.888_891DFVK>E LGG 10 5948527 5948527 + Missense_Mutation SNP G G T TCGA-HT-7480-01A-11D-2086-08 TCGA-HT-7480-10A-01D-2086-08 g.chr10:5948527G>T c.685G>T c.(685-687)Gtg>Ttg p.V229L LGG 10 5979128 5979128 + Missense_Mutation SNP G G A TCGA-HT-7692-01A-12D-2253-08 TCGA-HT-7692-10A-01D-2253-08 g.chr10:5979128G>A c.3017G>A c.(3016-3018)cGc>cAc p.R1006H LIHC 10 5945032 5945032 + Missense_Mutation SNP G G C TCGA-CC-A8HT-01A-11D-A35Z-10 TCGA-CC-A8HT-10A-01D-A35Z-10 g.chr10:5945032G>C c.51G>C c.(49-51)ttG>ttC p.L17F LIHC 10 5945116 5945116 + Silent SNP G G C TCGA-UB-A7ME-01A-11D-A33K-10 TCGA-UB-A7ME-10A-01D-A33K-10 g.chr10:5945116G>C c.135G>C c.(133-135)ccG>ccC p.P45P LIHC 10 5948067 5948067 + Missense_Mutation SNP G G T TCGA-2Y-A9HA-01A-11D-A38X-10 TCGA-2Y-A9HA-10A-01D-A38X-10 g.chr10:5948067G>T c.225G>T c.(223-225)atG>atT p.M75I LIHC 10 5952981 5952981 + Silent SNP C C T TCGA-K7-AAU7-01A-11D-A382-10 TCGA-K7-AAU7-10A-01D-A385-10 g.chr10:5952981C>T c.1101C>T c.(1099-1101)tgC>tgT p.C367C LUAD 10 5937145 5937145 + Intron SNP C C T TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr10:5937145C>T LUAD 10 5948121 5948121 + Missense_Mutation SNP G G T TCGA-75-6206-01A-11D-1753-08 TCGA-75-6206-10A-01D-1753-08 g.chr10:5948121G>T c.279G>T c.(277-279)atG>atT p.M93I LUAD 10 5948241 5948241 + Missense_Mutation SNP G G T TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr10:5948241G>T c.399G>T c.(397-399)caG>caT p.Q133H LUAD 10 5948307 5948307 + Silent SNP A A T TCGA-78-7542-01A-21D-2063-08 TCGA-78-7542-11A-01D-2063-08 g.chr10:5948307A>T c.465A>T c.(463-465)ccA>ccT p.P155P LUAD 10 5948591 5948591 + Missense_Mutation SNP C C A TCGA-80-5608-01A-31D-1945-08 TCGA-80-5608-10A-01D-1946-08 g.chr10:5948591C>A c.749C>A c.(748-750)cCg>cAg p.P250Q LUAD 10 5955787 5955787 + Missense_Mutation SNP C C T TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr10:5955787C>T c.1289C>T c.(1288-1290)cCa>cTa p.P430L LUAD 10 5955790 5955790 + Missense_Mutation SNP C C T TCGA-05-4395-01A-01D-1265-08 TCGA-05-4395-10A-01D-1265-08 g.chr10:5955790C>T c.1292C>T c.(1291-1293)tCt>tTt p.S431F LUAD 10 5956140 5956140 + Splice_Site SNP G G T TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr10:5956140G>T c.e8-1 LUAD 10 5956210 5956210 + Silent SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr10:5956210G>T c.1374G>T c.(1372-1374)gtG>gtT p.V458V LUAD 10 5956210 5956210 + Silent SNP G G T TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr10:5956210G>T c.1374G>T c.(1372-1374)gtG>gtT p.V458V LUAD 10 5957452 5957452 + Missense_Mutation SNP G G T TCGA-55-7576-01A-11D-2063-08 TCGA-55-7576-10A-01D-2063-08 g.chr10:5957452G>T c.1483G>T c.(1483-1485)Gca>Tca p.A495S LUAD 10 5960326 5960326 + Missense_Mutation SNP C C G TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr10:5960326C>G c.1985C>G c.(1984-1986)tCt>tGt p.S662C LUAD 10 5960359 5960359 + Missense_Mutation SNP C C A TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr10:5960359C>A c.2018C>A c.(2017-2019)cCg>cAg p.P673Q LUAD 10 5965635 5965635 + Nonsense_Mutation SNP C C T TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr10:5965635C>T c.2374C>T c.(2374-2376)Cag>Tag p.Q792* LUAD 10 5965660 5965660 + Splice_Site SNP G G T TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chr10:5965660G>T c.e16+1 LUAD 10 5969492 5969492 + Silent SNP G G A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr10:5969492G>A c.2817G>A c.(2815-2817)ttG>ttA p.L939L LUAD 10 5978452 5978452 + Missense_Mutation SNP G G A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr10:5978452G>A c.2863G>A c.(2863-2865)Gtc>Atc p.V955I LUAD 10 5978520 5978520 + Silent SNP C C G TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr10:5978520C>G c.2931C>G c.(2929-2931)gtC>gtG p.V977V LUSC 10 5948139 5948139 + Silent SNP C C T TCGA-43-6770-01A-11D-1817-08 TCGA-43-6770-11A-01D-1817-08 g.chr10:5948139C>T c.297C>T c.(295-297)agC>agT p.S99S LUSC 10 5959446 5959446 + Missense_Mutation SNP G G A TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chr10:5959446G>A c.1852G>A c.(1852-1854)Gag>Aag p.E618K LUSC 10 5979143 5979143 + Missense_Mutation SNP C C A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr10:5979143C>A c.3032C>A c.(3031-3033)gCg>gAg p.A1011E OV 10 5948332 5948332 + Nonsense_Mutation SNP C C T TCGA-24-1847-01A-01W-0633-09 TCGA-24-1847-10A-01W-0634-09 g.chr10:5948332C>T c.490C>T c.(490-492)Caa>Taa p.Q164* OV 10 5948407 5948407 + Missense_Mutation SNP C C G TCGA-13-2065-01A-01D-1526-09 TCGA-13-2065-10A-01D-1526-09 g.chr10:5948407C>G c.565C>G c.(565-567)Cct>Gct p.P189A OV 10 5958363 5958363 + Missense_Mutation SNP A A T TCGA-13-0890-01A-01W-0421-09 TCGA-13-0890-10A-01W-0421-09 g.chr10:5958363A>T c.1732A>T c.(1732-1734)Att>Ttt p.I578F OV 10 5969461 5969461 + Missense_Mutation SNP T T G TCGA-61-1727-01A-01W-0639-09 TCGA-61-1727-11A-01W-0639-09 g.chr10:5969461T>G c.2786T>G c.(2785-2787)cTc>cGc p.L929R OV 10 5978419 5978419 + Splice_Site SNP G G C TCGA-23-1122-01A-01W-0486-08 TCGA-23-1122-10A-01W-0486-08 g.chr10:5978419G>C c.2830G>C c.(2830-2832)Gag>Cag p.E944Q PAAD 10 5945034 5945034 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:5945034C>T c.53C>T c.(52-54)gCt>gTt p.A18V PAAD 10 5948357 5948357 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:5948357G>A c.515G>A c.(514-516)cGg>cAg p.R172Q PAAD 10 5956233 5956233 + Splice_Site SNP G G A TCGA-HZ-A77O-01A-11D-A33T-08 TCGA-HZ-A77O-10A-01D-A33W-08 g.chr10:5956233G>A c.e8+1 PCPG 10 5960389 5960389 + Missense_Mutation SNP C C T TCGA-QR-A6GR-01A-11D-A35D-08 TCGA-QR-A6GR-10A-01D-A35B-08 g.chr10:5960389C>T c.2048C>T c.(2047-2049)gCg>gTg p.A683V PRAD 10 5948526 5948526 + Silent SNP G G A TCGA-CH-5754-01A-11D-1576-08 TCGA-CH-5754-10A-01D-1576-08 g.chr10:5948526G>A c.684G>A c.(682-684)ccG>ccA p.P228P PRAD 10 5955734 5955734 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:5955734C>T c.1236C>T c.(1234-1236)tgC>tgT p.C412C PRAD 10 5960417 5960417 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:5960417C>T c.2076C>T c.(2074-2076)caC>caT p.H692H PRAD 10 5966434 5966434 + Missense_Mutation SNP G G T TCGA-TP-A8TV-01A-11D-A41K-08 TCGA-TP-A8TV-10A-01D-A41N-08 g.chr10:5966434G>T c.2559G>T c.(2557-2559)agG>agT p.R853S PRAD 10 5979235 5979235 + Missense_Mutation SNP G G A TCGA-EJ-5510-01A-01D-1576-08 TCGA-EJ-5510-10A-01D-1577-08 g.chr10:5979235G>A c.3124G>A c.(3124-3126)Gtc>Atc p.V1042I SARC 10 5959430 5959430 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr10:5959430G>A c.1836G>A c.(1834-1836)ctG>ctA p.L612L SARC 10 5979192 5979192 + Silent SNP G G A TCGA-DX-AB2O-01A-12D-A38Z-09 TCGA-DX-AB2O-10A-01D-A38Z-09 g.chr10:5979192G>A c.3081G>A c.(3079-3081)gtG>gtA p.V1027V SKCM 10 5937086 5937086 + Intron SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr10:5937086C>T SKCM 10 5948022 5948022 + Silent SNP C C T TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr10:5948022C>T c.180C>T c.(178-180)atC>atT p.I60I SKCM 10 5948180 5948180 + Missense_Mutation SNP C C T TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr10:5948180C>T c.338C>T c.(337-339)tCa>tTa p.S113L SKCM 10 5950915 5950915 + Nonsense_Mutation SNP C C T TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr10:5950915C>T c.781C>T c.(781-783)Cga>Tga p.R261* SKCM 10 5951148 5951148 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:5951148C>T c.911C>T c.(910-912)cCg>cTg p.P304L SKCM 10 5951255 5951255 + Missense_Mutation SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr10:5951255G>A c.1018G>A c.(1018-1020)Ggg>Agg p.G340R SKCM 10 5951256 5951256 + Splice_Site SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr10:5951256G>A c.1019G>A c.(1018-1020)gGg>gAg p.G340E SKCM 10 5953047 5953047 + Silent SNP G G T TCGA-DA-A3F5-06A-11D-A20D-08 TCGA-DA-A3F5-10A-01D-A20D-08 g.chr10:5953047G>T c.1167G>T c.(1165-1167)gtG>gtT p.V389V SKCM 10 5956154 5956154 + Nonsense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr10:5956154C>T c.1318C>T c.(1318-1320)Caa>Taa p.Q440* SKCM 10 5958258 5958258 + Missense_Mutation SNP C C T TCGA-EE-A2GE-06A-11D-A196-08 TCGA-EE-A2GE-10A-01D-A198-08 g.chr10:5958258C>T c.1627C>T c.(1627-1629)Ctt>Ttt p.L543F SKCM 10 5960343 5960343 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr10:5960343A>C c.2002A>C c.(2002-2004)Atc>Ctc p.I668L SKCM 10 5960373 5960373 + Missense_Mutation SNP T T A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr10:5960373T>A c.2032T>A c.(2032-2034)Tat>Aat p.Y678N SKCM 10 5963508 5963508 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:5963508C>T c.2298C>T c.(2296-2298)ttC>ttT p.F766F SKCM 10 5969458 5969458 + Missense_Mutation SNP G G A TCGA-DA-A3F5-06A-11D-A20D-08 TCGA-DA-A3F5-10A-01D-A20D-08 g.chr10:5969458G>A c.2783G>A c.(2782-2784)cGt>cAt p.R928H SKCM 10 5979147 5979147 + Silent SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr10:5979147C>T c.3036C>T c.(3034-3036)ttC>ttT p.F1012F SKCM 10 5979201 5979201 + Silent SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr10:5979201C>T c.3090C>T c.(3088-3090)atC>atT p.I1030I

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 5945065 5945065 single base substitution C A 5_prime_UTR_variant BLCA-US 10 5945065 5945065 single base substitution C A exon_variant BLCA-US 10 5945065 5945065 single base substitution C A intron_variant BLCA-US 10 5945065 5945065 single base substitution C A missense_variant F28L 84C>A BLCA-US 10 5945065 5945065 single base substitution C A missense_variant F79L 237C>A BLCA-US 10 5945065 5945065 single base substitution C A upstream_gene_variant BLCA-US 10 5951204 5951204 single base substitution G A 5_prime_UTR_variant BLCA-US 10 5951204 5951204 single base substitution G A downstream_gene_variant BLCA-US 10 5951204 5951204 single base substitution G A exon_variant BLCA-US 10 5951204 5951204 single base substitution G A missense_variant E323K 967G>A BLCA-US 10 5951204 5951204 single base substitution G A missense_variant E374K 1120G>A BLCA-US 10 5951204 5951204 single base substitution G A upstream_gene_variant BLCA-US 10 5955750 5955750 single base substitution A T 5_prime_UTR_variant BLCA-US 10 5955750 5955750 single base substitution A T downstream_gene_variant BLCA-US 10 5955750 5955750 single base substitution A T missense_variant N418Y 1252A>T BLCA-US 10 5955750 5955750 single base substitution A T missense_variant N469Y 1405A>T BLCA-US 10 5955750 5955750 single base substitution A T upstream_gene_variant BLCA-US 10 5959443 5959443 single base substitution G C downstream_gene_variant BLCA-US 10 5959443 5959443 single base substitution G C exon_variant BLCA-US 10 5959443 5959443 single base substitution G C missense_variant E104Q 310G>C BLCA-US 10 5959443 5959443 single base substitution G C missense_variant E617Q 1849G>C BLCA-US 10 5959443 5959443 single base substitution G C missense_variant E668Q 2002G>C BLCA-US 10 5959443 5959443 single base substitution G C upstream_gene_variant BRCA-EU 10 5926909 5926909 single base substitution T C upstream_gene_variant BRCA-EU 10 5928218 5928218 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 5929324 5929324 single base substitution A C upstream_gene_variant BRCA-EU 10 5930099 5930099 single base substitution C G upstream_gene_variant BRCA-EU 10 5932291 5932291 single base substitution C T 5_prime_UTR_variant BRCA-EU 10 5932291 5932291 single base substitution C T exon_variant BRCA-EU 10 5932291 5932291 single base substitution C T intron_variant BRCA-EU 10 5932291 5932291 single base substitution C T upstream_gene_variant BRCA-EU 10 5932982 5932982 single base substitution T G intron_variant BRCA-EU 10 5932982 5932982 single base substitution T G splice_region_variant BRCA-EU 10 5932982 5932982 single base substitution T G upstream_gene_variant BRCA-EU 10 5933325 5933325 single base substitution C G intron_variant BRCA-EU 10 5933325 5933325 single base substitution C G upstream_gene_variant BRCA-EU 10 5933581 5933581 single base substitution T C intron_variant BRCA-EU 10 5933581 5933581 single base substitution T C upstream_gene_variant BRCA-EU 10 5934025 5934025 single base substitution C G intron_variant BRCA-EU 10 5934025 5934025 single base substitution C G upstream_gene_variant BRCA-EU 10 5934182 5934188 deletion of <=200bp GTCACAT - intron_variant BRCA-EU 10 5934182 5934188 deletion of <=200bp GTCACAT - upstream_gene_variant BRCA-EU 10 5936027 5936027 single base substitution G A intron_variant BRCA-EU 10 5936027 5936027 single base substitution G A upstream_gene_variant BRCA-EU 10 5936843 5936843 single base substitution C A intron_variant BRCA-EU 10 5937180 5937180 single base substitution C T intron_variant BRCA-EU 10 5937304 5937304 deletion of <=200bp T - intron_variant BRCA-EU 10 5937812 5937812 single base substitution T A intron_variant BRCA-EU 10 5938177 5938177 single base substitution C G intron_variant BRCA-EU 10 5940419 5940419 single base substitution G A intron_variant BRCA-EU 10 5940419 5940419 single base substitution G A upstream_gene_variant BRCA-EU 10 5940731 5940731 single base substitution C G intron_variant BRCA-EU 10 5940731 5940731 single base substitution C G upstream_gene_variant BRCA-EU 10 5942415 5942415 single base substitution G A intron_variant BRCA-EU 10 5942415 5942415 single base substitution G A upstream_gene_variant BRCA-EU 10 5942725 5942725 single base substitution C A intron_variant BRCA-EU 10 5942725 5942725 single base substitution C A upstream_gene_variant BRCA-EU 10 5944109 5944109 single base substitution G A intron_variant BRCA-EU 10 5944109 5944109 single base substitution G A upstream_gene_variant BRCA-EU 10 5944235 5944235 deletion of <=200bp T - intron_variant BRCA-EU 10 5944235 5944235 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 5944949 5944949 single base substitution T C intron_variant BRCA-EU 10 5944949 5944949 single base substitution T C upstream_gene_variant BRCA-EU 10 5945358 5945358 single base substitution A C intron_variant BRCA-EU 10 5945358 5945358 single base substitution A C upstream_gene_variant BRCA-EU 10 5947568 5947568 single base substitution G T intron_variant BRCA-EU 10 5947568 5947568 single base substitution G T upstream_gene_variant BRCA-EU 10 5948287 5948287 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 10 5948287 5948287 single base substitution C T exon_variant BRCA-EU 10 5948287 5948287 single base substitution C T missense_variant R149W 445C>T BRCA-EU 10 5948287 5948287 single base substitution C T missense_variant R200W 598C>T BRCA-EU 10 5948287 5948287 single base substitution C T upstream_gene_variant BRCA-EU 10 5951175 5951175 single base substitution G A 5_prime_UTR_variant BRCA-EU 10 5951175 5951175 single base substitution G A downstream_gene_variant BRCA-EU 10 5951175 5951175 single base substitution G A exon_variant BRCA-EU 10 5951175 5951175 single base substitution G A stop_gained W313* 938G>A BRCA-EU 10 5951175 5951175 single base substitution G A stop_gained W364* 1091G>A BRCA-EU 10 5951175 5951175 single base substitution G A upstream_gene_variant BRCA-EU 10 5953532 5953532 single base substitution C T downstream_gene_variant BRCA-EU 10 5953532 5953532 single base substitution C T intron_variant BRCA-EU 10 5953532 5953532 single base substitution C T upstream_gene_variant BRCA-EU 10 5954425 5954435 deletion of <=200bp TGCAGCCATCC - downstream_gene_variant BRCA-EU 10 5954425 5954435 deletion of <=200bp TGCAGCCATCC - intron_variant BRCA-EU 10 5954425 5954435 deletion of <=200bp TGCAGCCATCC - upstream_gene_variant BRCA-EU 10 5955303 5955303 single base substitution G T downstream_gene_variant BRCA-EU 10 5955303 5955303 single base substitution G T intron_variant BRCA-EU 10 5955303 5955303 single base substitution G T upstream_gene_variant BRCA-EU 10 5956026 5956026 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 5956026 5956026 deletion of <=200bp T - intron_variant BRCA-EU 10 5956026 5956026 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 5956664 5956664 single base substitution C G downstream_gene_variant BRCA-EU 10 5956664 5956664 single base substitution C G intron_variant BRCA-EU 10 5956664 5956664 single base substitution C G upstream_gene_variant BRCA-EU 10 5956786 5956786 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 5956786 5956786 deletion of <=200bp T - intron_variant BRCA-EU 10 5956786 5956786 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 5957582 5957582 single base substitution G A downstream_gene_variant BRCA-EU 10 5957582 5957582 single base substitution G A exon_variant BRCA-EU 10 5957582 5957582 single base substitution G A intron_variant BRCA-EU 10 5957582 5957582 single base substitution G A upstream_gene_variant BRCA-EU 10 5958222 5958222 single base substitution C G downstream_gene_variant BRCA-EU 10 5958222 5958222 single base substitution C G missense_variant L18V 52C>G BRCA-EU 10 5958222 5958222 single base substitution C G missense_variant L531V 1591C>G BRCA-EU 10 5958222 5958222 single base substitution C G missense_variant L582V 1744C>G BRCA-EU 10 5958222 5958222 single base substitution C G upstream_gene_variant BRCA-EU 10 5961449 5961449 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 5961449 5961449 deletion of <=200bp A - intron_variant BRCA-EU 10 5961449 5961449 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 5962055 5962055 single base substitution G T downstream_gene_variant BRCA-EU 10 5962055 5962055 single base substitution G T intron_variant BRCA-EU 10 5962055 5962055 single base substitution G T upstream_gene_variant BRCA-EU 10 5962153 5962153 deletion of <=200bp G - downstream_gene_variant BRCA-EU 10 5962153 5962153 deletion of <=200bp G - intron_variant BRCA-EU 10 5962153 5962153 deletion of <=200bp G - upstream_gene_variant BRCA-EU 10 5963469 5963469 single base substitution C T downstream_gene_variant BRCA-EU 10 5963469 5963469 single base substitution C T exon_variant BRCA-EU 10 5963469 5963469 single base substitution C T synonymous_variant N240N 720C>T BRCA-EU 10 5963469 5963469 single base substitution C T synonymous_variant N753N 2259C>T BRCA-EU 10 5963469 5963469 single base substitution C T synonymous_variant N804N 2412C>T BRCA-EU 10 5963469 5963469 single base substitution C T upstream_gene_variant BRCA-EU 10 5965188 5965188 single base substitution C T intron_variant BRCA-EU 10 5965188 5965188 single base substitution C T upstream_gene_variant BRCA-EU 10 5965918 5965918 single base substitution C T exon_variant BRCA-EU 10 5965918 5965918 single base substitution C T intron_variant BRCA-EU 10 5965918 5965918 single base substitution C T upstream_gene_variant BRCA-EU 10 5970805 5970810 deletion of <=200bp TAAGTG - downstream_gene_variant BRCA-EU 10 5970805 5970810 deletion of <=200bp TAAGTG - intron_variant BRCA-EU 10 5970810 5970810 single base substitution G T downstream_gene_variant BRCA-EU 10 5970810 5970810 single base substitution G T intron_variant BRCA-EU 10 5971949 5971949 single base substitution G C downstream_gene_variant BRCA-EU 10 5971949 5971949 single base substitution G C intron_variant BRCA-EU 10 5972889 5972889 single base substitution T G downstream_gene_variant BRCA-EU 10 5972889 5972889 single base substitution T G intron_variant BRCA-EU 10 5972894 5972894 single base substitution T G downstream_gene_variant BRCA-EU 10 5972894 5972894 single base substitution T G intron_variant BRCA-EU 10 5975149 5975149 single base substitution A G downstream_gene_variant BRCA-EU 10 5975149 5975149 single base substitution A G intron_variant BRCA-EU 10 5975149 5975149 single base substitution A G upstream_gene_variant BRCA-EU 10 5975898 5975898 single base substitution A G downstream_gene_variant BRCA-EU 10 5975898 5975898 single base substitution A G intron_variant BRCA-EU 10 5975898 5975898 single base substitution A G upstream_gene_variant BRCA-EU 10 5976970 5976970 single base substitution G A intron_variant BRCA-EU 10 5976970 5976970 single base substitution G A upstream_gene_variant BRCA-EU 10 5977128 5977128 deletion of <=200bp A - intron_variant BRCA-EU 10 5977128 5977128 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 5977782 5977782 single base substitution G A intron_variant BRCA-EU 10 5977782 5977782 single base substitution G A upstream_gene_variant BRCA-EU 10 5978466 5978466 single base substitution C T exon_variant BRCA-EU 10 5978466 5978466 single base substitution C T synonymous_variant G1010G 3030C>T BRCA-EU 10 5978466 5978466 single base substitution C T synonymous_variant G463G 1389C>T BRCA-EU 10 5978466 5978466 single base substitution C T synonymous_variant G959G 2877C>T BRCA-EU 10 5978466 5978466 single base substitution C T upstream_gene_variant BRCA-EU 10 5979245 5979245 single base substitution G C 3_prime_UTR_variant BRCA-EU 10 5979245 5979245 single base substitution G C downstream_gene_variant BRCA-EU 10 5979245 5979245 single base substitution G C exon_variant BRCA-EU 10 5980617 5980617 single base substitution G A downstream_gene_variant BRCA-EU 10 5980683 5980683 single base substitution G C downstream_gene_variant BRCA-EU 10 5981240 5981240 single base substitution G A downstream_gene_variant BRCA-EU 10 5981625 5981625 single base substitution G A downstream_gene_variant BRCA-EU 10 5982255 5982255 single base substitution G C downstream_gene_variant BRCA-EU 10 5983261 5983261 single base substitution G T downstream_gene_variant BRCA-EU 10 5983599 5983599 single base substitution C G downstream_gene_variant BRCA-EU 10 5984071 5984071 single base substitution C T downstream_gene_variant BRCA-EU 10 5984540 5984540 single base substitution C G downstream_gene_variant BRCA-FR 10 5933325 5933325 single base substitution C G intron_variant BRCA-FR 10 5933325 5933325 single base substitution C G upstream_gene_variant BRCA-FR 10 5938177 5938177 single base substitution C G intron_variant BRCA-FR 10 5946791 5946791 single base substitution C A intron_variant BRCA-FR 10 5946791 5946791 single base substitution C A upstream_gene_variant BRCA-FR 10 5956664 5956664 single base substitution C G downstream_gene_variant BRCA-FR 10 5956664 5956664 single base substitution C G intron_variant BRCA-FR 10 5956664 5956664 single base substitution C G upstream_gene_variant BRCA-FR 10 5957582 5957582 single base substitution G A downstream_gene_variant BRCA-FR 10 5957582 5957582 single base substitution G A exon_variant BRCA-FR 10 5957582 5957582 single base substitution G A intron_variant BRCA-FR 10 5957582 5957582 single base substitution G A upstream_gene_variant BRCA-FR 10 5961088 5961088 single base substitution C T downstream_gene_variant BRCA-FR 10 5961088 5961088 single base substitution C T intron_variant BRCA-FR 10 5961088 5961088 single base substitution C T upstream_gene_variant BRCA-FR 10 5981240 5981240 single base substitution G A downstream_gene_variant BRCA-KR 10 5956204 5956204 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-KR 10 5956204 5956204 single base substitution C G downstream_gene_variant BRCA-KR 10 5956204 5956204 single base substitution C G exon_variant BRCA-KR 10 5956204 5956204 single base substitution C G synonymous_variant L456L 1368C>G BRCA-KR 10 5956204 5956204 single base substitution C G synonymous_variant L507L 1521C>G BRCA-KR 10 5956204 5956204 single base substitution C G upstream_gene_variant BRCA-UK 10 5959475 5959475 single base substitution G C downstream_gene_variant BRCA-UK 10 5959475 5959475 single base substitution G C intron_variant BRCA-UK 10 5959475 5959475 single base substitution G C splice_region_variant BRCA-UK 10 5959475 5959475 single base substitution G C upstream_gene_variant BRCA-UK 10 5959577 5959577 single base substitution G T downstream_gene_variant BRCA-UK 10 5959577 5959577 single base substitution G T exon_variant BRCA-UK 10 5959577 5959577 single base substitution G T missense_variant S121I 362G>T BRCA-UK 10 5959577 5959577 single base substitution G T missense_variant S634I 1901G>T BRCA-UK 10 5959577 5959577 single base substitution G T missense_variant S685I 2054G>T BRCA-UK 10 5959577 5959577 single base substitution G T upstream_gene_variant BRCA-UK 10 5959578 5959578 single base substitution C T downstream_gene_variant BRCA-UK 10 5959578 5959578 single base substitution C T exon_variant BRCA-UK 10 5959578 5959578 single base substitution C T synonymous_variant S121S 363C>T BRCA-UK 10 5959578 5959578 single base substitution C T synonymous_variant S634S 1902C>T BRCA-UK 10 5959578 5959578 single base substitution C T synonymous_variant S685S 2055C>T BRCA-UK 10 5959578 5959578 single base substitution C T upstream_gene_variant BRCA-US 10 5930026 5930026 single base substitution G A upstream_gene_variant BRCA-US 10 5937117 5937117 single base substitution G T intron_variant BRCA-US 10 5937117 5937117 single base substitution G T missense_variant A41S 121G>T BRCA-US 10 5945053 5945053 single base substitution G A 5_prime_UTR_variant BRCA-US 10 5945053 5945053 single base substitution G A exon_variant BRCA-US 10 5945053 5945053 single base substitution G A intron_variant BRCA-US 10 5945053 5945053 single base substitution G A synonymous_variant V24V 72G>A BRCA-US 10 5945053 5945053 single base substitution G A synonymous_variant V75V 225G>A BRCA-US 10 5945053 5945053 single base substitution G A upstream_gene_variant BRCA-US 10 5945069 5945069 single base substitution C T 5_prime_UTR_variant BRCA-US 10 5945069 5945069 single base substitution C T exon_variant BRCA-US 10 5945069 5945069 single base substitution C T intron_variant BRCA-US 10 5945069 5945069 single base substitution C T stop_gained Q30* 88C>T BRCA-US 10 5945069 5945069 single base substitution C T stop_gained Q81* 241C>T BRCA-US 10 5945069 5945069 single base substitution C T upstream_gene_variant BRCA-US 10 5945078 5945081 deletion of <=200bp ACAA - 5_prime_UTR_variant BRCA-US 10 5945078 5945081 deletion of <=200bp ACAA - exon_variant BRCA-US 10 5945078 5945081 deletion of <=200bp ACAA - frameshift_variant TN33 BRCA-US 10 5945078 5945081 deletion of <=200bp ACAA - frameshift_variant TN84 BRCA-US 10 5945078 5945081 deletion of <=200bp ACAA - intron_variant BRCA-US 10 5945078 5945081 deletion of <=200bp ACAA - upstream_gene_variant BRCA-US 10 5948163 5948163 deletion of <=200bp C - 5_prime_UTR_variant BRCA-US 10 5948163 5948163 deletion of <=200bp C - exon_variant BRCA-US 10 5948163 5948163 deletion of <=200bp C - frameshift_variant G107 BRCA-US 10 5948163 5948163 deletion of <=200bp C - frameshift_variant G158 BRCA-US 10 5948163 5948163 deletion of <=200bp C - upstream_gene_variant BRCA-US 10 5948251 5948251 single base substitution A C 5_prime_UTR_variant BRCA-US 10 5948251 5948251 single base substitution A C exon_variant BRCA-US 10 5948251 5948251 single base substitution A C missense_variant T137P 409A>C BRCA-US 10 5948251 5948251 single base substitution A C missense_variant T188P 562A>C BRCA-US 10 5948251 5948251 single base substitution A C upstream_gene_variant BRCA-US 10 5948419 5948419 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 10 5948419 5948419 single base substitution C G exon_variant BRCA-US 10 5948419 5948419 single base substitution C G missense_variant P193A 577C>G BRCA-US 10 5948419 5948419 single base substitution C G missense_variant P244A 730C>G BRCA-US 10 5948419 5948419 single base substitution C G upstream_gene_variant BRCA-US 10 5951018 5951018 single base substitution G A downstream_gene_variant BRCA-US 10 5951018 5951018 single base substitution G A missense_variant R295Q 884G>A BRCA-US 10 5951018 5951018 single base substitution G A missense_variant R346Q 1037G>A BRCA-US 10 5951018 5951018 single base substitution G A splice_region_variant BRCA-US 10 5951233 5951233 single base substitution C A 5_prime_UTR_variant BRCA-US 10 5951233 5951233 single base substitution C A downstream_gene_variant BRCA-US 10 5951233 5951233 single base substitution C A exon_variant BRCA-US 10 5951233 5951233 single base substitution C A synonymous_variant L332L 996C>A BRCA-US 10 5951233 5951233 single base substitution C A synonymous_variant L383L 1149C>A BRCA-US 10 5951233 5951233 single base substitution C A upstream_gene_variant BRCA-US 10 5963220 5963220 single base substitution G T downstream_gene_variant BRCA-US 10 5963220 5963220 single base substitution G T splice_acceptor_variant BRCA-US 10 5963220 5963220 single base substitution G T upstream_gene_variant BRCA-US 10 5969465 5969465 single base substitution C G downstream_gene_variant BRCA-US 10 5969465 5969465 single base substitution C G exon_variant BRCA-US 10 5969465 5969465 single base substitution C G missense_variant I434M 1302C>G BRCA-US 10 5969465 5969465 single base substitution C G missense_variant I930M 2790C>G BRCA-US 10 5969465 5969465 single base substitution C G missense_variant I981M 2943C>G BTCA-JP 10 5936488 5936488 single base substitution G T intron_variant BTCA-JP 10 5948366 5948366 single base substitution C A 5_prime_UTR_variant BTCA-JP 10 5948366 5948366 single base substitution C A exon_variant BTCA-JP 10 5948366 5948366 single base substitution C A missense_variant A175E 524C>A BTCA-JP 10 5948366 5948366 single base substitution C A missense_variant A226E 677C>A BTCA-JP 10 5948366 5948366 single base substitution C A upstream_gene_variant BTCA-JP 10 5957403 5957403 single base substitution G T 5_prime_UTR_variant BTCA-JP 10 5957403 5957403 single base substitution G T downstream_gene_variant BTCA-JP 10 5957403 5957403 single base substitution G T exon_variant BTCA-JP 10 5957403 5957403 single base substitution G T missense_variant E478D 1434G>T BTCA-JP 10 5957403 5957403 single base substitution G T missense_variant E529D 1587G>T BTCA-JP 10 5957403 5957403 single base substitution G T upstream_gene_variant BTCA-JP 10 5963615 5963615 single base substitution G A downstream_gene_variant BTCA-JP 10 5963615 5963615 single base substitution G A intron_variant BTCA-JP 10 5963615 5963615 single base substitution G A upstream_gene_variant CESC-US 10 5945069 5945069 single base substitution C T 5_prime_UTR_variant CESC-US 10 5945069 5945069 single base substitution C T exon_variant CESC-US 10 5945069 5945069 single base substitution C T intron_variant CESC-US 10 5945069 5945069 single base substitution C T stop_gained Q30* 88C>T CESC-US 10 5945069 5945069 single base substitution C T stop_gained Q81* 241C>T CESC-US 10 5945069 5945069 single base substitution C T upstream_gene_variant CESC-US 10 5957376 5957376 single base substitution G A 5_prime_UTR_variant CESC-US 10 5957376 5957376 single base substitution G A downstream_gene_variant CESC-US 10 5957376 5957376 single base substitution G A exon_variant CESC-US 10 5957376 5957376 single base substitution G A synonymous_variant K469K 1407G>A CESC-US 10 5957376 5957376 single base substitution G A synonymous_variant K520K 1560G>A CESC-US 10 5957376 5957376 single base substitution G A upstream_gene_variant CESC-US 10 5963484 5963484 single base substitution C T downstream_gene_variant CESC-US 10 5963484 5963484 single base substitution C T exon_variant CESC-US 10 5963484 5963484 single base substitution C T synonymous_variant A245A 735C>T CESC-US 10 5963484 5963484 single base substitution C T synonymous_variant A758A 2274C>T CESC-US 10 5963484 5963484 single base substitution C T synonymous_variant A809A 2427C>T CESC-US 10 5963484 5963484 single base substitution C T upstream_gene_variant CLLE-ES 10 5954473 5954473 single base substitution A G downstream_gene_variant CLLE-ES 10 5954473 5954473 single base substitution A G intron_variant CLLE-ES 10 5954473 5954473 single base substitution A G upstream_gene_variant CLLE-ES 10 5967422 5967422 single base substitution C T downstream_gene_variant CLLE-ES 10 5967422 5967422 single base substitution C T exon_variant CLLE-ES 10 5967422 5967422 single base substitution C T missense_variant H401Y 1201C>T CLLE-ES 10 5967422 5967422 single base substitution C T missense_variant H897Y 2689C>T CLLE-ES 10 5967422 5967422 single base substitution C T missense_variant H948Y 2842C>T CLLE-ES 10 5971274 5971274 single base substitution A T downstream_gene_variant CLLE-ES 10 5971274 5971274 single base substitution A T intron_variant COAD-US 10 5931035 5931035 single base substitution C T upstream_gene_variant COAD-US 10 5931230 5931230 single base substitution C T upstream_gene_variant COAD-US 10 5948209 5948209 single base substitution C T 5_prime_UTR_variant COAD-US 10 5948209 5948209 single base substitution C T exon_variant COAD-US 10 5948209 5948209 single base substitution C T missense_variant R123W 367C>T COAD-US 10 5948209 5948209 single base substitution C T missense_variant R174W 520C>T COAD-US 10 5948209 5948209 single base substitution C T upstream_gene_variant COAD-US 10 5948356 5948356 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COAD-US 10 5948356 5948356 single base substitution C T exon_variant COAD-US 10 5948356 5948356 single base substitution C T missense_variant R172W 514C>T COAD-US 10 5948356 5948356 single base substitution C T missense_variant R223W 667C>T COAD-US 10 5948356 5948356 single base substitution C T upstream_gene_variant COAD-US 10 5953003 5953003 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 10 5953003 5953003 single base substitution G A downstream_gene_variant COAD-US 10 5953003 5953003 single base substitution G A missense_variant V375M 1123G>A COAD-US 10 5953003 5953003 single base substitution G A missense_variant V426M 1276G>A COAD-US 10 5953003 5953003 single base substitution G A upstream_gene_variant COAD-US 10 5959402 5959402 single base substitution G A downstream_gene_variant COAD-US 10 5959402 5959402 single base substitution G A exon_variant COAD-US 10 5959402 5959402 single base substitution G A missense_variant S603N 1808G>A COAD-US 10 5959402 5959402 single base substitution G A missense_variant S654N 1961G>A COAD-US 10 5959402 5959402 single base substitution G A missense_variant S90N 269G>A COAD-US 10 5959402 5959402 single base substitution G A upstream_gene_variant COAD-US 10 5960396 5960396 single base substitution C T downstream_gene_variant COAD-US 10 5960396 5960396 single base substitution C T synonymous_variant N172N 516C>T COAD-US 10 5960396 5960396 single base substitution C T synonymous_variant N685N 2055C>T COAD-US 10 5960396 5960396 single base substitution C T synonymous_variant N736N 2208C>T COAD-US 10 5960396 5960396 single base substitution C T upstream_gene_variant COAD-US 10 5978452 5978452 single base substitution G A exon_variant COAD-US 10 5978452 5978452 single base substitution G A missense_variant V1006I 3016G>A COAD-US 10 5978452 5978452 single base substitution G A missense_variant V459I 1375G>A COAD-US 10 5978452 5978452 single base substitution G A missense_variant V955I 2863G>A COAD-US 10 5978452 5978452 single base substitution G A upstream_gene_variant COAD-US 10 5978484 5978484 single base substitution G A exon_variant COAD-US 10 5978484 5978484 single base substitution G A synonymous_variant V1016V 3048G>A COAD-US 10 5978484 5978484 single base substitution G A synonymous_variant V469V 1407G>A COAD-US 10 5978484 5978484 single base substitution G A synonymous_variant V965V 2895G>A COAD-US 10 5978484 5978484 single base substitution G A upstream_gene_variant COAD-US 10 5978510 5978510 single base substitution T C exon_variant COAD-US 10 5978510 5978510 single base substitution T C missense_variant V1025A 3074T>C COAD-US 10 5978510 5978510 single base substitution T C missense_variant V478A 1433T>C COAD-US 10 5978510 5978510 single base substitution T C missense_variant V974A 2921T>C COAD-US 10 5978510 5978510 single base substitution T C upstream_gene_variant COAD-US 10 5979158 5979158 deletion of <=200bp C - downstream_gene_variant COAD-US 10 5979158 5979158 deletion of <=200bp C - frameshift_variant S1016 COAD-US 10 5979158 5979158 deletion of <=200bp C - frameshift_variant S1067 COAD-US 10 5979158 5979158 deletion of <=200bp C - frameshift_variant S520 COAD-US 10 5979158 5979158 deletion of <=200bp C - intron_variant COCA-CN 10 5934141 5934141 single base substitution G T intron_variant COCA-CN 10 5934141 5934141 single base substitution G T upstream_gene_variant COCA-CN 10 5948639 5948639 single base substitution G A downstream_gene_variant COCA-CN 10 5948639 5948639 single base substitution G A intron_variant COCA-CN 10 5951019 5951019 single base substitution G A downstream_gene_variant COCA-CN 10 5951019 5951019 single base substitution G A splice_donor_variant COCA-CN 10 5952901 5952901 single base substitution G A downstream_gene_variant COCA-CN 10 5952901 5952901 single base substitution G A missense_variant G341S 1021G>A COCA-CN 10 5952901 5952901 single base substitution G A missense_variant G392S 1174G>A COCA-CN 10 5952901 5952901 single base substitution G A splice_region_variant COCA-CN 10 5952901 5952901 single base substitution G A upstream_gene_variant COCA-CN 10 5953056 5953056 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 10 5953056 5953056 single base substitution C T downstream_gene_variant COCA-CN 10 5953056 5953056 single base substitution C T synonymous_variant Y392Y 1176C>T COCA-CN 10 5953056 5953056 single base substitution C T synonymous_variant Y443Y 1329C>T COCA-CN 10 5953056 5953056 single base substitution C T upstream_gene_variant COCA-CN 10 5957464 5957464 single base substitution G A 5_prime_UTR_variant COCA-CN 10 5957464 5957464 single base substitution G A downstream_gene_variant COCA-CN 10 5957464 5957464 single base substitution G A exon_variant COCA-CN 10 5957464 5957464 single base substitution G A missense_variant E499K 1495G>A COCA-CN 10 5957464 5957464 single base substitution G A missense_variant E550K 1648G>A COCA-CN 10 5957464 5957464 single base substitution G A upstream_gene_variant COCA-CN 10 5959469 5959469 single base substitution C T downstream_gene_variant COCA-CN 10 5959469 5959469 single base substitution C T splice_region_variant COCA-CN 10 5959469 5959469 single base substitution C T upstream_gene_variant COCA-CN 10 5959490 5959490 single base substitution C T downstream_gene_variant COCA-CN 10 5959490 5959490 single base substitution C T intron_variant COCA-CN 10 5959490 5959490 single base substitution C T upstream_gene_variant COCA-CN 10 5963391 5963391 single base substitution T G downstream_gene_variant COCA-CN 10 5963391 5963391 single base substitution T G intron_variant COCA-CN 10 5963391 5963391 single base substitution T G upstream_gene_variant COCA-CN 10 5967176 5967176 single base substitution C T downstream_gene_variant COCA-CN 10 5967176 5967176 single base substitution C T intron_variant COCA-CN 10 5967176 5967176 single base substitution C T upstream_gene_variant COCA-CN 10 5968082 5968082 single base substitution C A downstream_gene_variant COCA-CN 10 5968082 5968082 single base substitution C A intron_variant COCA-CN 10 5976338 5976338 single base substitution T G downstream_gene_variant COCA-CN 10 5976338 5976338 single base substitution T G intron_variant COCA-CN 10 5976338 5976338 single base substitution T G upstream_gene_variant COCA-CN 10 5976339 5976339 single base substitution G T downstream_gene_variant COCA-CN 10 5976339 5976339 single base substitution G T intron_variant COCA-CN 10 5976339 5976339 single base substitution G T upstream_gene_variant COCA-CN 10 5978169 5978169 single base substitution A G intron_variant COCA-CN 10 5978169 5978169 single base substitution A G upstream_gene_variant COCA-CN 10 5978545 5978545 single base substitution A G exon_variant COCA-CN 10 5978545 5978545 single base substitution A G missense_variant T1037A 3109A>G COCA-CN 10 5978545 5978545 single base substitution A G missense_variant T490A 1468A>G COCA-CN 10 5978545 5978545 single base substitution A G missense_variant T986A 2956A>G COCA-CN 10 5978545 5978545 single base substitution A G upstream_gene_variant COCA-CN 10 5979256 5979256 single base substitution C T 3_prime_UTR_variant COCA-CN 10 5979256 5979256 single base substitution C T downstream_gene_variant COCA-CN 10 5979256 5979256 single base substitution C T exon_variant COCA-CN 10 5979496 5979496 single base substitution A T 3_prime_UTR_variant COCA-CN 10 5979496 5979496 single base substitution A T downstream_gene_variant EOPC-DE 10 5969899 5969899 single base substitution G A downstream_gene_variant EOPC-DE 10 5969899 5969899 single base substitution G A intron_variant ESAD-UK 10 5931838 5931838 single base substitution G A intron_variant ESAD-UK 10 5931838 5931838 single base substitution G A upstream_gene_variant ESAD-UK 10 5931839 5931839 single base substitution C G intron_variant ESAD-UK 10 5931839 5931839 single base substitution C G upstream_gene_variant ESAD-UK 10 5934400 5934400 single base substitution C T intron_variant ESAD-UK 10 5934400 5934400 single base substitution C T upstream_gene_variant ESAD-UK 10 5934896 5934896 single base substitution C T intron_variant ESAD-UK 10 5934896 5934896 single base substitution C T upstream_gene_variant ESAD-UK 10 5936503 5936503 single base substitution C T intron_variant ESAD-UK 10 5941274 5941278 deletion of <=200bp TTTGT - intron_variant ESAD-UK 10 5941274 5941278 deletion of <=200bp TTTGT - upstream_gene_variant ESAD-UK 10 5945394 5945394 single base substitution A C intron_variant ESAD-UK 10 5945394 5945394 single base substitution A C upstream_gene_variant ESAD-UK 10 5956911 5956911 single base substitution G C downstream_gene_variant ESAD-UK 10 5956911 5956911 single base substitution G C intron_variant ESAD-UK 10 5956911 5956911 single base substitution G C upstream_gene_variant ESAD-UK 10 5956966 5956966 single base substitution G A downstream_gene_variant ESAD-UK 10 5956966 5956966 single base substitution G A intron_variant ESAD-UK 10 5956966 5956966 single base substitution G A upstream_gene_variant ESAD-UK 10 5959339 5959339 single base substitution G T downstream_gene_variant ESAD-UK 10 5959339 5959339 single base substitution G T exon_variant ESAD-UK 10 5959339 5959339 single base substitution G T intron_variant ESAD-UK 10 5959339 5959339 single base substitution G T upstream_gene_variant ESAD-UK 10 5964536 5964536 single base substitution A G downstream_gene_variant ESAD-UK 10 5964536 5964536 single base substitution A G intron_variant ESAD-UK 10 5964536 5964536 single base substitution A G upstream_gene_variant ESAD-UK 10 5965007 5965007 single base substitution G A intron_variant ESAD-UK 10 5965007 5965007 single base substitution G A upstream_gene_variant ESAD-UK 10 5965990 5965990 single base substitution A G exon_variant ESAD-UK 10 5965990 5965990 single base substitution A G intron_variant ESAD-UK 10 5965990 5965990 single base substitution A G upstream_gene_variant ESAD-UK 10 5967072 5967072 single base substitution G T downstream_gene_variant ESAD-UK 10 5967072 5967072 single base substitution G T intron_variant ESAD-UK 10 5967072 5967072 single base substitution G T upstream_gene_variant ESAD-UK 10 5967236 5967236 single base substitution G A downstream_gene_variant ESAD-UK 10 5967236 5967236 single base substitution G A exon_variant ESAD-UK 10 5967236 5967236 single base substitution G A intron_variant ESAD-UK 10 5967236 5967236 single base substitution G A upstream_gene_variant ESAD-UK 10 5971459 5971459 single base substitution C A downstream_gene_variant ESAD-UK 10 5971459 5971459 single base substitution C A exon_variant ESAD-UK 10 5971459 5971459 single base substitution C A intron_variant ESAD-UK 10 5974170 5974170 single base substitution A T downstream_gene_variant ESAD-UK 10 5974170 5974170 single base substitution A T intron_variant ESAD-UK 10 5974170 5974170 single base substitution A T upstream_gene_variant ESAD-UK 10 5975105 5975105 single base substitution C T downstream_gene_variant ESAD-UK 10 5975105 5975105 single base substitution C T intron_variant ESAD-UK 10 5975105 5975105 single base substitution C T upstream_gene_variant ESAD-UK 10 5975893 5975893 single base substitution G C downstream_gene_variant ESAD-UK 10 5975893 5975893 single base substitution G C intron_variant ESAD-UK 10 5975893 5975893 single base substitution G C upstream_gene_variant ESAD-UK 10 5978757 5978757 single base substitution G A intron_variant ESAD-UK 10 5980588 5980588 single base substitution G A downstream_gene_variant ESAD-UK 10 5982624 5982624 deletion of <=200bp C - downstream_gene_variant ESAD-UK 10 5983811 5983811 single base substitution G C downstream_gene_variant ESCA-CN 10 5937036 5937036 single base substitution C T intron_variant ESCA-CN 10 5937036 5937036 single base substitution C T stop_gained Q14* 40C>T ESCA-CN 10 5948657 5948657 single base substitution C T downstream_gene_variant ESCA-CN 10 5948657 5948657 single base substitution C T intron_variant ESCA-CN 10 5957391 5957391 single base substitution C G 5_prime_UTR_variant ESCA-CN 10 5957391 5957391 single base substitution C G downstream_gene_variant ESCA-CN 10 5957391 5957391 single base substitution C G exon_variant ESCA-CN 10 5957391 5957391 single base substitution C G synonymous_variant V474V 1422C>G ESCA-CN 10 5957391 5957391 single base substitution C G synonymous_variant V525V 1575C>G ESCA-CN 10 5957391 5957391 single base substitution C G upstream_gene_variant ESCA-CN 10 5967177 5967177 single base substitution G A downstream_gene_variant ESCA-CN 10 5967177 5967177 single base substitution G A intron_variant ESCA-CN 10 5967177 5967177 single base substitution G A upstream_gene_variant GBM-US 10 5929963 5929963 single base substitution C T upstream_gene_variant KIRC-US 10 5937075 5937075 single base substitution G T intron_variant KIRC-US 10 5937075 5937075 single base substitution G T missense_variant G27W 79G>T KIRC-US 10 5948166 5948166 single base substitution T C 5_prime_UTR_variant KIRC-US 10 5948166 5948166 single base substitution T C exon_variant KIRC-US 10 5948166 5948166 single base substitution T C synonymous_variant S108S 324T>C KIRC-US 10 5948166 5948166 single base substitution T C synonymous_variant S159S 477T>C KIRC-US 10 5948166 5948166 single base substitution T C upstream_gene_variant KIRC-US 10 5951142 5951142 single base substitution G A 5_prime_UTR_variant KIRC-US 10 5951142 5951142 single base substitution G A downstream_gene_variant KIRC-US 10 5951142 5951142 single base substitution G A exon_variant KIRC-US 10 5951142 5951142 single base substitution G A missense_variant C302Y 905G>A KIRC-US 10 5951142 5951142 single base substitution G A missense_variant C353Y 1058G>A KIRC-US 10 5951142 5951142 single base substitution G A upstream_gene_variant KIRC-US 10 5953065 5953070 deletion of <=200bp GGAGAA - 5_prime_UTR_variant KIRC-US 10 5953065 5953070 deletion of <=200bp GGAGAA - downstream_gene_variant KIRC-US 10 5953065 5953070 deletion of <=200bp GGAGAA - inframe_deletion REK395R KIRC-US 10 5953065 5953070 deletion of <=200bp GGAGAA - inframe_deletion REK446R KIRC-US 10 5953065 5953070 deletion of <=200bp GGAGAA - upstream_gene_variant KIRC-US 10 5963284 5963284 single base substitution G A downstream_gene_variant KIRC-US 10 5963284 5963284 single base substitution G A missense_variant V209I 625G>A KIRC-US 10 5963284 5963284 single base substitution G A missense_variant V722I 2164G>A KIRC-US 10 5963284 5963284 single base substitution G A missense_variant V773I 2317G>A KIRC-US 10 5963284 5963284 single base substitution G A upstream_gene_variant KIRC-US 10 5967396 5967404 deletion of <=200bp ATTTTGTGA - disruptive_inframe_deletion DFVK392E KIRC-US 10 5967396 5967404 deletion of <=200bp ATTTTGTGA - disruptive_inframe_deletion DFVK888E KIRC-US 10 5967396 5967404 deletion of <=200bp ATTTTGTGA - disruptive_inframe_deletion DFVK939E KIRC-US 10 5967396 5967404 deletion of <=200bp ATTTTGTGA - downstream_gene_variant KIRC-US 10 5967396 5967404 deletion of <=200bp ATTTTGTGA - exon_variant LAML-KR 10 5936413 5936413 single base substitution G C 5_prime_UTR_variant LAML-KR 10 5936413 5936413 single base substitution G C intron_variant LAML-KR 10 5936565 5936565 single base substitution C A intron_variant LAML-KR 10 5958575 5958575 single base substitution G A downstream_gene_variant LAML-KR 10 5958575 5958575 single base substitution G A intron_variant LAML-KR 10 5958575 5958575 single base substitution G A upstream_gene_variant LGG-US 10 5948527 5948527 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LGG-US 10 5948527 5948527 single base substitution G T exon_variant LGG-US 10 5948527 5948527 single base substitution G T missense_variant V229L 685G>T LGG-US 10 5948527 5948527 single base substitution G T missense_variant V280L 838G>T LGG-US 10 5979128 5979128 single base substitution G A downstream_gene_variant LGG-US 10 5979128 5979128 single base substitution G A intron_variant LGG-US 10 5979128 5979128 single base substitution G A missense_variant R1006H 3017G>A LGG-US 10 5979128 5979128 single base substitution G A missense_variant R1057H 3170G>A LGG-US 10 5979128 5979128 single base substitution G A missense_variant R510H 1529G>A LICA-CN 10 5931046 5931046 single base substitution A T upstream_gene_variant LICA-CN 10 5960319 5960319 single base substitution G A downstream_gene_variant LICA-CN 10 5960319 5960319 single base substitution G A missense_variant V147I 439G>A LICA-CN 10 5960319 5960319 single base substitution G A missense_variant V660I 1978G>A LICA-CN 10 5960319 5960319 single base substitution G A missense_variant V711I 2131G>A LICA-CN 10 5960319 5960319 single base substitution G A upstream_gene_variant LICA-FR 10 5926703 5926703 insertion of <=200bp - AA upstream_gene_variant LICA-FR 10 5937446 5937446 single base substitution A G intron_variant LICA-FR 10 5956098 5956098 single base substitution A C downstream_gene_variant LICA-FR 10 5956098 5956098 single base substitution A C intron_variant LICA-FR 10 5956098 5956098 single base substitution A C upstream_gene_variant LICA-FR 10 5958348 5958348 single base substitution A G downstream_gene_variant LICA-FR 10 5958348 5958348 single base substitution A G missense_variant I573V 1717A>G LICA-FR 10 5958348 5958348 single base substitution A G missense_variant I60V 178A>G LICA-FR 10 5958348 5958348 single base substitution A G missense_variant I624V 1870A>G LICA-FR 10 5958348 5958348 single base substitution A G upstream_gene_variant LICA-FR 10 5965655 5965655 single base substitution G A exon_variant LICA-FR 10 5965655 5965655 single base substitution G A synonymous_variant R285R 855G>A LICA-FR 10 5965655 5965655 single base substitution G A synonymous_variant R798R 2394G>A LICA-FR 10 5965655 5965655 single base substitution G A synonymous_variant R849R 2547G>A LICA-FR 10 5965655 5965655 single base substitution G A upstream_gene_variant LICA-FR 10 5968294 5968294 single base substitution C T downstream_gene_variant LICA-FR 10 5968294 5968294 single base substitution C T intron_variant LIHC-US 10 5945116 5945116 single base substitution G C 5_prime_UTR_variant LIHC-US 10 5945116 5945116 single base substitution G C exon_variant LIHC-US 10 5945116 5945116 single base substitution G C intron_variant LIHC-US 10 5945116 5945116 single base substitution G C synonymous_variant P45P 135G>C LIHC-US 10 5945116 5945116 single base substitution G C synonymous_variant P96P 288G>C LIHC-US 10 5945116 5945116 single base substitution G C upstream_gene_variant LIHC-US 10 5945117 5945117 single base substitution A T 5_prime_UTR_variant LIHC-US 10 5945117 5945117 single base substitution A T exon_variant LIHC-US 10 5945117 5945117 single base substitution A T intron_variant LIHC-US 10 5945117 5945117 single base substitution A T stop_gained R46* 136A>T LIHC-US 10 5945117 5945117 single base substitution A T stop_gained R97* 289A>T LIHC-US 10 5945117 5945117 single base substitution A T upstream_gene_variant LINC-JP 10 5927731 5927735 deletion of <=200bp GGGAG - upstream_gene_variant LINC-JP 10 5934509 5934509 single base substitution A G intron_variant LINC-JP 10 5934509 5934509 single base substitution A G upstream_gene_variant LINC-JP 10 5942718 5942718 single base substitution A G intron_variant LINC-JP 10 5942718 5942718 single base substitution A G upstream_gene_variant LINC-JP 10 5958518 5958518 single base substitution G A downstream_gene_variant LINC-JP 10 5958518 5958518 single base substitution G A intron_variant LINC-JP 10 5958518 5958518 single base substitution G A upstream_gene_variant LINC-JP 10 5958552 5958552 single base substitution G A downstream_gene_variant LINC-JP 10 5958552 5958552 single base substitution G A intron_variant LINC-JP 10 5958552 5958552 single base substitution G A upstream_gene_variant LINC-JP 10 5958616 5958616 single base substitution G A downstream_gene_variant LINC-JP 10 5958616 5958616 single base substitution G A intron_variant LINC-JP 10 5958616 5958616 single base substitution G A upstream_gene_variant LINC-JP 10 5960307 5960307 single base substitution A G downstream_gene_variant LINC-JP 10 5960307 5960307 single base substitution A G missense_variant I143V 427A>G LINC-JP 10 5960307 5960307 single base substitution A G missense_variant I656V 1966A>G LINC-JP 10 5960307 5960307 single base substitution A G missense_variant I707V 2119A>G LINC-JP 10 5960307 5960307 single base substitution A G upstream_gene_variant LIRI-JP 10 5927976 5927976 single base substitution T C upstream_gene_variant LIRI-JP 10 5928655 5928655 single base substitution A G upstream_gene_variant LIRI-JP 10 5929069 5929069 single base substitution T C upstream_gene_variant LIRI-JP 10 5933089 5933091 deletion of <=200bp TCT - intron_variant LIRI-JP 10 5933089 5933091 deletion of <=200bp TCT - upstream_gene_variant LIRI-JP 10 5933399 5933399 single base substitution C A intron_variant LIRI-JP 10 5933399 5933399 single base substitution C A upstream_gene_variant LIRI-JP 10 5936294 5936294 single base substitution T C intron_variant LIRI-JP 10 5936294 5936294 single base substitution T C upstream_gene_variant LIRI-JP 10 5938246 5938246 single base substitution T C intron_variant LIRI-JP 10 5939806 5939806 single base substitution A G intron_variant LIRI-JP 10 5941933 5941933 single base substitution A G intron_variant LIRI-JP 10 5941933 5941933 single base substitution A G upstream_gene_variant LIRI-JP 10 5942274 5942274 single base substitution A G intron_variant LIRI-JP 10 5942274 5942274 single base substitution A G upstream_gene_variant LIRI-JP 10 5942371 5942371 single base substitution G A intron_variant LIRI-JP 10 5942371 5942371 single base substitution G A upstream_gene_variant LIRI-JP 10 5945078 5945081 deletion of <=200bp ACAA - 5_prime_UTR_variant LIRI-JP 10 5945078 5945081 deletion of <=200bp ACAA - exon_variant LIRI-JP 10 5945078 5945081 deletion of <=200bp ACAA - frameshift_variant TN33 LIRI-JP 10 5945078 5945081 deletion of <=200bp ACAA - frameshift_variant TN84 LIRI-JP 10 5945078 5945081 deletion of <=200bp ACAA - intron_variant LIRI-JP 10 5945078 5945081 deletion of <=200bp ACAA - upstream_gene_variant LIRI-JP 10 5945252 5945252 insertion of <=200bp - T intron_variant LIRI-JP 10 5945252 5945252 insertion of <=200bp - T upstream_gene_variant LIRI-JP 10 5945358 5945358 single base substitution A G intron_variant LIRI-JP 10 5945358 5945358 single base substitution A G upstream_gene_variant LIRI-JP 10 5946407 5946407 single base substitution A G intron_variant LIRI-JP 10 5946407 5946407 single base substitution A G upstream_gene_variant LIRI-JP 10 5947205 5947205 single base substitution C T exon_variant LIRI-JP 10 5947205 5947205 single base substitution C T intron_variant LIRI-JP 10 5947205 5947205 single base substitution C T upstream_gene_variant LIRI-JP 10 5952233 5952233 single base substitution A G downstream_gene_variant LIRI-JP 10 5952233 5952233 single base substitution A G intron_variant LIRI-JP 10 5952233 5952233 single base substitution A G upstream_gene_variant LIRI-JP 10 5953202 5953202 single base substitution A G downstream_gene_variant LIRI-JP 10 5953202 5953202 single base substitution A G intron_variant LIRI-JP 10 5953202 5953202 single base substitution A G upstream_gene_variant LIRI-JP 10 5956161 5956161 single base substitution C A 5_prime_UTR_variant LIRI-JP 10 5956161 5956161 single base substitution C A downstream_gene_variant LIRI-JP 10 5956161 5956161 single base substitution C A exon_variant LIRI-JP 10 5956161 5956161 single base substitution C A missense_variant T442K 1325C>A LIRI-JP 10 5956161 5956161 single base substitution C A missense_variant T493K 1478C>A LIRI-JP 10 5956161 5956161 single base substitution C A upstream_gene_variant LIRI-JP 10 5956186 5956186 single base substitution T A 5_prime_UTR_variant LIRI-JP 10 5956186 5956186 single base substitution T A downstream_gene_variant LIRI-JP 10 5956186 5956186 single base substitution T A exon_variant LIRI-JP 10 5956186 5956186 single base substitution T A missense_variant N450K 1350T>A LIRI-JP 10 5956186 5956186 single base substitution T A missense_variant N501K 1503T>A LIRI-JP 10 5956186 5956186 single base substitution T A upstream_gene_variant LIRI-JP 10 5956786 5956786 insertion of <=200bp - T downstream_gene_variant LIRI-JP 10 5956786 5956786 insertion of <=200bp - T intron_variant LIRI-JP 10 5956786 5956786 insertion of <=200bp - T upstream_gene_variant LIRI-JP 10 5957635 5957635 single base substitution G A downstream_gene_variant LIRI-JP 10 5957635 5957635 single base substitution G A exon_variant LIRI-JP 10 5957635 5957635 single base substitution G A intron_variant LIRI-JP 10 5957635 5957635 single base substitution G A upstream_gene_variant LIRI-JP 10 5957998 5957998 single base substitution G T downstream_gene_variant LIRI-JP 10 5957998 5957998 single base substitution G T intron_variant LIRI-JP 10 5957998 5957998 single base substitution G T upstream_gene_variant LIRI-JP 10 5957999 5957999 single base substitution G T downstream_gene_variant LIRI-JP 10 5957999 5957999 single base substitution G T intron_variant LIRI-JP 10 5957999 5957999 single base substitution G T upstream_gene_variant LIRI-JP 10 5959011 5959011 single base substitution T G downstream_gene_variant LIRI-JP 10 5959011 5959011 single base substitution T G intron_variant LIRI-JP 10 5959011 5959011 single base substitution T G upstream_gene_variant LIRI-JP 10 5959056 5959056 deletion of <=200bp T - downstream_gene_variant LIRI-JP 10 5959056 5959056 deletion of <=200bp T - exon_variant LIRI-JP 10 5959056 5959056 deletion of <=200bp T - intron_variant LIRI-JP 10 5959056 5959056 deletion of <=200bp T - upstream_gene_variant LIRI-JP 10 5959263 5959263 single base substitution G T downstream_gene_variant LIRI-JP 10 5959263 5959263 single base substitution G T exon_variant LIRI-JP 10 5959263 5959263 single base substitution G T intron_variant LIRI-JP 10 5959263 5959263 single base substitution G T upstream_gene_variant LIRI-JP 10 5961847 5961847 single base substitution A T downstream_gene_variant LIRI-JP 10 5961847 5961847 single base substitution A T intron_variant LIRI-JP 10 5961847 5961847 single base substitution A T upstream_gene_variant LIRI-JP 10 5961870 5961870 single base substitution A G downstream_gene_variant LIRI-JP 10 5961870 5961870 single base substitution A G intron_variant LIRI-JP 10 5961870 5961870 single base substitution A G upstream_gene_variant LIRI-JP 10 5962409 5962409 single base substitution A G downstream_gene_variant LIRI-JP 10 5962409 5962409 single base substitution A G intron_variant LIRI-JP 10 5962409 5962409 single base substitution A G upstream_gene_variant LIRI-JP 10 5963057 5963057 single base substitution A G downstream_gene_variant LIRI-JP 10 5963057 5963057 single base substitution A G intron_variant LIRI-JP 10 5963057 5963057 single base substitution A G upstream_gene_variant LIRI-JP 10 5963563 5963563 single base substitution G A downstream_gene_variant LIRI-JP 10 5963563 5963563 single base substitution G A intron_variant LIRI-JP 10 5963563 5963563 single base substitution G A upstream_gene_variant LIRI-JP 10 5964476 5964476 single base substitution A G downstream_gene_variant LIRI-JP 10 5964476 5964476 single base substitution A G intron_variant LIRI-JP 10 5964476 5964476 single base substitution A G upstream_gene_variant LIRI-JP 10 5966909 5966909 single base substitution T G downstream_gene_variant LIRI-JP 10 5966909 5966909 single base substitution T G intron_variant LIRI-JP 10 5966909 5966909 single base substitution T G upstream_gene_variant LIRI-JP 10 5968391 5968391 single base substitution A G downstream_gene_variant LIRI-JP 10 5968391 5968391 single base substitution A G intron_variant LIRI-JP 10 5969238 5969238 single base substitution A C downstream_gene_variant LIRI-JP 10 5969238 5969238 single base substitution A C intron_variant LIRI-JP 10 5970819 5970819 single base substitution A G downstream_gene_variant LIRI-JP 10 5970819 5970819 single base substitution A G intron_variant LIRI-JP 10 5970883 5970883 single base substitution A C downstream_gene_variant LIRI-JP 10 5970883 5970883 single base substitution A C intron_variant LIRI-JP 10 5972008 5972008 single base substitution T C downstream_gene_variant LIRI-JP 10 5972008 5972008 single base substitution T C intron_variant LIRI-JP 10 5972476 5972476 single base substitution T G downstream_gene_variant LIRI-JP 10 5972476 5972476 single base substitution T G intron_variant LIRI-JP 10 5973564 5973564 single base substitution A G downstream_gene_variant LIRI-JP 10 5973564 5973564 single base substitution A G intron_variant LIRI-JP 10 5974304 5974304 single base substitution A C downstream_gene_variant LIRI-JP 10 5974304 5974304 single base substitution A C intron_variant LIRI-JP 10 5974304 5974304 single base substitution A C upstream_gene_variant LIRI-JP 10 5974672 5974672 single base substitution T C downstream_gene_variant LIRI-JP 10 5974672 5974672 single base substitution T C intron_variant LIRI-JP 10 5974672 5974672 single base substitution T C upstream_gene_variant LIRI-JP 10 5975732 5975732 single base substitution A C downstream_gene_variant LIRI-JP 10 5975732 5975732 single base substitution A C intron_variant LIRI-JP 10 5975732 5975732 single base substitution A C upstream_gene_variant LIRI-JP 10 5975971 5975971 single base substitution A C downstream_gene_variant LIRI-JP 10 5975971 5975971 single base substitution A C intron_variant LIRI-JP 10 5975971 5975971 single base substitution A C upstream_gene_variant LIRI-JP 10 5977850 5977850 single base substitution T G intron_variant LIRI-JP 10 5977850 5977850 single base substitution T G upstream_gene_variant LIRI-JP 10 5978452 5978452 single base substitution G A exon_variant LIRI-JP 10 5978452 5978452 single base substitution G A missense_variant V1006I 3016G>A LIRI-JP 10 5978452 5978452 single base substitution G A missense_variant V459I 1375G>A LIRI-JP 10 5978452 5978452 single base substitution G A missense_variant V955I 2863G>A LIRI-JP 10 5978452 5978452 single base substitution G A upstream_gene_variant LIRI-JP 10 5980924 5980941 deletion of <=200bp CAGTGATCCTGGAGGCAT - downstream_gene_variant LIRI-JP 10 5983421 5983421 single base substitution T C downstream_gene_variant LIRI-JP 10 5983719 5983719 single base substitution C A downstream_gene_variant LUSC-KR 10 5931479 5931479 single base substitution C A upstream_gene_variant LUSC-KR 10 5932441 5932441 single base substitution G A intron_variant LUSC-KR 10 5932441 5932441 single base substitution G A upstream_gene_variant LUSC-KR 10 5932626 5932626 single base substitution G A intron_variant LUSC-KR 10 5932626 5932626 single base substitution G A upstream_gene_variant LUSC-KR 10 5935975 5935975 single base substitution T C intron_variant LUSC-KR 10 5935975 5935975 single base substitution T C upstream_gene_variant LUSC-KR 10 5936501 5936501 single base substitution A C intron_variant LUSC-KR 10 5937105 5937105 single base substitution C T intron_variant LUSC-KR 10 5937105 5937105 single base substitution C T stop_gained Q37* 109C>T LUSC-KR 10 5940535 5940535 single base substitution G A intron_variant LUSC-KR 10 5940535 5940535 single base substitution G A upstream_gene_variant LUSC-KR 10 5947248 5947248 single base substitution G T intron_variant LUSC-KR 10 5947248 5947248 single base substitution G T splice_region_variant LUSC-KR 10 5947248 5947248 single base substitution G T upstream_gene_variant LUSC-KR 10 5948959 5948959 single base substitution A T downstream_gene_variant LUSC-KR 10 5948959 5948959 single base substitution A T intron_variant LUSC-KR 10 5958532 5958532 single base substitution A G downstream_gene_variant LUSC-KR 10 5958532 5958532 single base substitution A G intron_variant LUSC-KR 10 5958532 5958532 single base substitution A G upstream_gene_variant LUSC-KR 10 5958931 5958931 single base substitution G T downstream_gene_variant LUSC-KR 10 5958931 5958931 single base substitution G T intron_variant LUSC-KR 10 5958931 5958931 single base substitution G T upstream_gene_variant LUSC-US 10 5929903 5929903 single base substitution C T upstream_gene_variant LUSC-US 10 5948139 5948139 single base substitution C T 5_prime_UTR_variant LUSC-US 10 5948139 5948139 single base substitution C T exon_variant LUSC-US 10 5948139 5948139 single base substitution C T synonymous_variant S150S 450C>T LUSC-US 10 5948139 5948139 single base substitution C T synonymous_variant S99S 297C>T LUSC-US 10 5948139 5948139 single base substitution C T upstream_gene_variant LUSC-US 10 5959446 5959446 single base substitution G A downstream_gene_variant LUSC-US 10 5959446 5959446 single base substitution G A exon_variant LUSC-US 10 5959446 5959446 single base substitution G A missense_variant E105K 313G>A LUSC-US 10 5959446 5959446 single base substitution G A missense_variant E618K 1852G>A LUSC-US 10 5959446 5959446 single base substitution G A missense_variant E669K 2005G>A LUSC-US 10 5959446 5959446 single base substitution G A upstream_gene_variant LUSC-US 10 5979143 5979143 single base substitution C A downstream_gene_variant LUSC-US 10 5979143 5979143 single base substitution C A intron_variant LUSC-US 10 5979143 5979143 single base substitution C A missense_variant A1011E 3032C>A LUSC-US 10 5979143 5979143 single base substitution C A missense_variant A1062E 3185C>A LUSC-US 10 5979143 5979143 single base substitution C A missense_variant A515E 1544C>A MALY-DE 10 5932149 5932149 single base substitution C G intron_variant MALY-DE 10 5932149 5932149 single base substitution C G upstream_gene_variant MALY-DE 10 5935568 5935568 single base substitution A C intron_variant MALY-DE 10 5935568 5935568 single base substitution A C upstream_gene_variant MALY-DE 10 5937431 5937431 single base substitution C G intron_variant MALY-DE 10 5964870 5964871 deletion of <=200bp AG - intron_variant MALY-DE 10 5964870 5964871 deletion of <=200bp AG - upstream_gene_variant MALY-DE 10 5970773 5970773 single base substitution A C downstream_gene_variant MALY-DE 10 5970773 5970773 single base substitution A C intron_variant MALY-DE 10 5974542 5974542 insertion of <=200bp - T downstream_gene_variant MALY-DE 10 5974542 5974542 insertion of <=200bp - T intron_variant MALY-DE 10 5974542 5974542 insertion of <=200bp - T upstream_gene_variant MALY-DE 10 5976057 5976057 single base substitution A C downstream_gene_variant MALY-DE 10 5976057 5976057 single base substitution A C intron_variant MALY-DE 10 5976057 5976057 single base substitution A C upstream_gene_variant MALY-DE 10 5981274 5981274 single base substitution G A downstream_gene_variant MALY-DE 10 5982402 5982402 single base substitution A T downstream_gene_variant MELA-AU 10 5927987 5927987 single base substitution C T upstream_gene_variant MELA-AU 10 5928145 5928145 single base substitution C T upstream_gene_variant MELA-AU 10 5928189 5928190 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 5928243 5928243 single base substitution G A upstream_gene_variant MELA-AU 10 5928373 5928373 single base substitution G A upstream_gene_variant MELA-AU 10 5929009 5929009 single base substitution G A upstream_gene_variant MELA-AU 10 5929255 5929255 single base substitution G A upstream_gene_variant MELA-AU 10 5930127 5930127 single base substitution G A upstream_gene_variant MELA-AU 10 5931986 5931986 single base substitution G A intron_variant MELA-AU 10 5931986 5931986 single base substitution G A upstream_gene_variant MELA-AU 10 5931991 5931991 single base substitution G A intron_variant MELA-AU 10 5931991 5931991 single base substitution G A upstream_gene_variant MELA-AU 10 5932032 5932032 single base substitution C T intron_variant MELA-AU 10 5932032 5932032 single base substitution C T upstream_gene_variant MELA-AU 10 5932033 5932033 single base substitution C T intron_variant MELA-AU 10 5932033 5932033 single base substitution C T upstream_gene_variant MELA-AU 10 5932038 5932038 single base substitution G A intron_variant MELA-AU 10 5932038 5932038 single base substitution G A upstream_gene_variant MELA-AU 10 5932064 5932064 single base substitution G A intron_variant MELA-AU 10 5932064 5932064 single base substitution G A upstream_gene_variant MELA-AU 10 5932083 5932084 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 5932083 5932084 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 5932095 5932095 single base substitution G A intron_variant MELA-AU 10 5932095 5932095 single base substitution G A upstream_gene_variant MELA-AU 10 5932100 5932100 single base substitution C T intron_variant MELA-AU 10 5932100 5932100 single base substitution C T upstream_gene_variant MELA-AU 10 5932154 5932154 single base substitution C T intron_variant MELA-AU 10 5932154 5932154 single base substitution C T upstream_gene_variant MELA-AU 10 5933525 5933525 single base substitution C T intron_variant MELA-AU 10 5933525 5933525 single base substitution C T upstream_gene_variant MELA-AU 10 5933959 5933960 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 5933959 5933960 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 5934895 5934895 single base substitution C T intron_variant MELA-AU 10 5934895 5934895 single base substitution C T upstream_gene_variant MELA-AU 10 5934919 5934919 single base substitution C T intron_variant MELA-AU 10 5934919 5934919 single base substitution C T upstream_gene_variant MELA-AU 10 5935155 5935155 single base substitution G T intron_variant MELA-AU 10 5935155 5935155 single base substitution G T upstream_gene_variant MELA-AU 10 5935188 5935188 single base substitution G A intron_variant MELA-AU 10 5935188 5935188 single base substitution G A upstream_gene_variant MELA-AU 10 5935414 5935414 single base substitution T A intron_variant MELA-AU 10 5935414 5935414 single base substitution T A upstream_gene_variant MELA-AU 10 5935967 5935967 single base substitution C T intron_variant MELA-AU 10 5935967 5935967 single base substitution C T upstream_gene_variant MELA-AU 10 5937904 5937904 single base substitution T A intron_variant MELA-AU 10 5938287 5938287 single base substitution C T intron_variant MELA-AU 10 5939020 5939020 single base substitution T C intron_variant MELA-AU 10 5939354 5939354 single base substitution C T intron_variant MELA-AU 10 5939498 5939498 single base substitution C T intron_variant MELA-AU 10 5939635 5939635 single base substitution C T intron_variant MELA-AU 10 5939673 5939673 single base substitution C T intron_variant MELA-AU 10 5939869 5939869 single base substitution C T intron_variant MELA-AU 10 5939942 5939942 single base substitution C T intron_variant MELA-AU 10 5940358 5940358 single base substitution C T intron_variant MELA-AU 10 5940358 5940358 single base substitution C T upstream_gene_variant MELA-AU 10 5942397 5942397 single base substitution C T intron_variant MELA-AU 10 5942397 5942397 single base substitution C T upstream_gene_variant MELA-AU 10 5942941 5942942 multiple base substitution (>=2bp and <=200bp) TC CA intron_variant MELA-AU 10 5942941 5942942 multiple base substitution (>=2bp and <=200bp) TC CA upstream_gene_variant MELA-AU 10 5944552 5944552 single base substitution C T intron_variant MELA-AU 10 5944552 5944552 single base substitution C T upstream_gene_variant MELA-AU 10 5944643 5944643 single base substitution C T intron_variant MELA-AU 10 5944643 5944643 single base substitution C T upstream_gene_variant MELA-AU 10 5944650 5944650 single base substitution C A intron_variant MELA-AU 10 5944650 5944650 single base substitution C A upstream_gene_variant MELA-AU 10 5945610 5945610 single base substitution C T intron_variant MELA-AU 10 5945610 5945610 single base substitution C T upstream_gene_variant MELA-AU 10 5945973 5945973 single base substitution C T intron_variant MELA-AU 10 5945973 5945973 single base substitution C T upstream_gene_variant MELA-AU 10 5946356 5946356 single base substitution G T intron_variant MELA-AU 10 5946356 5946356 single base substitution G T upstream_gene_variant MELA-AU 10 5946368 5946368 single base substitution C T intron_variant MELA-AU 10 5946368 5946368 single base substitution C T upstream_gene_variant MELA-AU 10 5947053 5947053 single base substitution C T intron_variant MELA-AU 10 5947053 5947053 single base substitution C T upstream_gene_variant MELA-AU 10 5947207 5947207 single base substitution C T exon_variant MELA-AU 10 5947207 5947207 single base substitution C T intron_variant MELA-AU 10 5947207 5947207 single base substitution C T upstream_gene_variant MELA-AU 10 5947559 5947559 single base substitution C T intron_variant MELA-AU 10 5947559 5947559 single base substitution C T upstream_gene_variant MELA-AU 10 5948629 5948629 single base substitution C T downstream_gene_variant MELA-AU 10 5948629 5948629 single base substitution C T intron_variant MELA-AU 10 5948693 5948693 single base substitution C T downstream_gene_variant MELA-AU 10 5948693 5948693 single base substitution C T intron_variant MELA-AU 10 5948860 5948861 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 5948860 5948861 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 5949758 5949758 single base substitution C T downstream_gene_variant MELA-AU 10 5949758 5949758 single base substitution C T intron_variant MELA-AU 10 5950382 5950382 single base substitution C T downstream_gene_variant MELA-AU 10 5950382 5950382 single base substitution C T intron_variant MELA-AU 10 5952698 5952698 single base substitution C T downstream_gene_variant MELA-AU 10 5952698 5952698 single base substitution C T intron_variant MELA-AU 10 5952698 5952698 single base substitution C T upstream_gene_variant MELA-AU 10 5952846 5952846 single base substitution C T downstream_gene_variant MELA-AU 10 5952846 5952846 single base substitution C T intron_variant MELA-AU 10 5952846 5952846 single base substitution C T upstream_gene_variant MELA-AU 10 5952934 5952934 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 10 5952934 5952934 single base substitution G T downstream_gene_variant MELA-AU 10 5952934 5952934 single base substitution G T missense_variant V352L 1054G>T MELA-AU 10 5952934 5952934 single base substitution G T missense_variant V403L 1207G>T MELA-AU 10 5952934 5952934 single base substitution G T upstream_gene_variant MELA-AU 10 5953024 5953024 single base substitution G A 5_prime_UTR_variant MELA-AU 10 5953024 5953024 single base substitution G A downstream_gene_variant MELA-AU 10 5953024 5953024 single base substitution G A missense_variant E382K 1144G>A MELA-AU 10 5953024 5953024 single base substitution G A missense_variant E433K 1297G>A MELA-AU 10 5953024 5953024 single base substitution G A upstream_gene_variant MELA-AU 10 5953809 5953809 single base substitution G A downstream_gene_variant MELA-AU 10 5953809 5953809 single base substitution G A intron_variant MELA-AU 10 5953809 5953809 single base substitution G A upstream_gene_variant MELA-AU 10 5954210 5954210 single base substitution C T downstream_gene_variant MELA-AU 10 5954210 5954210 single base substitution C T intron_variant MELA-AU 10 5954210 5954210 single base substitution C T upstream_gene_variant MELA-AU 10 5954564 5954564 single base substitution C T downstream_gene_variant MELA-AU 10 5954564 5954564 single base substitution C T intron_variant MELA-AU 10 5954564 5954564 single base substitution C T upstream_gene_variant MELA-AU 10 5954811 5954811 single base substitution C T downstream_gene_variant MELA-AU 10 5954811 5954811 single base substitution C T intron_variant MELA-AU 10 5954811 5954811 single base substitution C T upstream_gene_variant MELA-AU 10 5955140 5955140 single base substitution C T downstream_gene_variant MELA-AU 10 5955140 5955140 single base substitution C T intron_variant MELA-AU 10 5955140 5955140 single base substitution C T upstream_gene_variant MELA-AU 10 5955465 5955465 single base substitution C A downstream_gene_variant MELA-AU 10 5955465 5955465 single base substitution C A intron_variant MELA-AU 10 5955465 5955465 single base substitution C A upstream_gene_variant MELA-AU 10 5955468 5955468 single base substitution C T downstream_gene_variant MELA-AU 10 5955468 5955468 single base substitution C T intron_variant MELA-AU 10 5955468 5955468 single base substitution C T upstream_gene_variant MELA-AU 10 5955584 5955584 single base substitution C T downstream_gene_variant MELA-AU 10 5955584 5955584 single base substitution C T intron_variant MELA-AU 10 5955584 5955584 single base substitution C T upstream_gene_variant MELA-AU 10 5956803 5956803 single base substitution C T downstream_gene_variant MELA-AU 10 5956803 5956803 single base substitution C T intron_variant MELA-AU 10 5956803 5956803 single base substitution C T upstream_gene_variant MELA-AU 10 5957839 5957839 single base substitution T C downstream_gene_variant MELA-AU 10 5957839 5957839 single base substitution T C exon_variant MELA-AU 10 5957839 5957839 single base substitution T C intron_variant MELA-AU 10 5957839 5957839 single base substitution T C upstream_gene_variant MELA-AU 10 5957869 5957869 single base substitution C T downstream_gene_variant MELA-AU 10 5957869 5957869 single base substitution C T exon_variant MELA-AU 10 5957869 5957869 single base substitution C T intron_variant MELA-AU 10 5957869 5957869 single base substitution C T upstream_gene_variant MELA-AU 10 5957930 5957930 single base substitution C T downstream_gene_variant MELA-AU 10 5957930 5957930 single base substitution C T intron_variant MELA-AU 10 5957930 5957930 single base substitution C T upstream_gene_variant MELA-AU 10 5957978 5957978 single base substitution C T downstream_gene_variant MELA-AU 10 5957978 5957978 single base substitution C T intron_variant MELA-AU 10 5957978 5957978 single base substitution C T upstream_gene_variant MELA-AU 10 5958692 5958692 single base substitution G A downstream_gene_variant MELA-AU 10 5958692 5958692 single base substitution G A intron_variant MELA-AU 10 5958692 5958692 single base substitution G A upstream_gene_variant MELA-AU 10 5959282 5959282 single base substitution T C downstream_gene_variant MELA-AU 10 5959282 5959282 single base substitution T C exon_variant MELA-AU 10 5959282 5959282 single base substitution T C intron_variant MELA-AU 10 5959282 5959282 single base substitution T C upstream_gene_variant MELA-AU 10 5960085 5960085 single base substitution C T downstream_gene_variant MELA-AU 10 5960085 5960085 single base substitution C T intron_variant MELA-AU 10 5960085 5960085 single base substitution C T upstream_gene_variant MELA-AU 10 5960174 5960174 single base substitution C A downstream_gene_variant MELA-AU 10 5960174 5960174 single base substitution C A intron_variant MELA-AU 10 5960174 5960174 single base substitution C A upstream_gene_variant MELA-AU 10 5961196 5961197 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 5961196 5961197 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 5961196 5961197 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 5962617 5962617 single base substitution C T downstream_gene_variant MELA-AU 10 5962617 5962617 single base substitution C T intron_variant MELA-AU 10 5962617 5962617 single base substitution C T upstream_gene_variant MELA-AU 10 5963071 5963071 single base substitution T C downstream_gene_variant MELA-AU 10 5963071 5963071 single base substitution T C intron_variant MELA-AU 10 5963071 5963071 single base substitution T C upstream_gene_variant MELA-AU 10 5963203 5963203 single base substitution C T downstream_gene_variant MELA-AU 10 5963203 5963203 single base substitution C T intron_variant MELA-AU 10 5963203 5963203 single base substitution C T upstream_gene_variant MELA-AU 10 5963365 5963365 single base substitution C T downstream_gene_variant MELA-AU 10 5963365 5963365 single base substitution C T intron_variant MELA-AU 10 5963365 5963365 single base substitution C T upstream_gene_variant MELA-AU 10 5964294 5964294 single base substitution C T downstream_gene_variant MELA-AU 10 5964294 5964294 single base substitution C T intron_variant MELA-AU 10 5964294 5964294 single base substitution C T upstream_gene_variant MELA-AU 10 5964560 5964560 single base substitution A T downstream_gene_variant MELA-AU 10 5964560 5964560 single base substitution A T intron_variant MELA-AU 10 5964560 5964560 single base substitution A T upstream_gene_variant MELA-AU 10 5964644 5964644 single base substitution C T intron_variant MELA-AU 10 5964644 5964644 single base substitution C T upstream_gene_variant MELA-AU 10 5964854 5964854 single base substitution T A intron_variant MELA-AU 10 5964854 5964854 single base substitution T A upstream_gene_variant MELA-AU 10 5965111 5965111 single base substitution G A intron_variant MELA-AU 10 5965111 5965111 single base substitution G A upstream_gene_variant MELA-AU 10 5965594 5965594 single base substitution C T exon_variant MELA-AU 10 5965594 5965594 single base substitution C T missense_variant S265L 794C>T MELA-AU 10 5965594 5965594 single base substitution C T missense_variant S778L 2333C>T MELA-AU 10 5965594 5965594 single base substitution C T missense_variant S829L 2486C>T MELA-AU 10 5965594 5965594 single base substitution C T upstream_gene_variant MELA-AU 10 5966029 5966029 single base substitution C T exon_variant MELA-AU 10 5966029 5966029 single base substitution C T intron_variant MELA-AU 10 5966029 5966029 single base substitution C T upstream_gene_variant MELA-AU 10 5966386 5966386 single base substitution C T downstream_gene_variant MELA-AU 10 5966386 5966386 single base substitution C T exon_variant MELA-AU 10 5966386 5966386 single base substitution C T synonymous_variant I324I 972C>T MELA-AU 10 5966386 5966386 single base substitution C T synonymous_variant I837I 2511C>T MELA-AU 10 5966386 5966386 single base substitution C T synonymous_variant I888I 2664C>T MELA-AU 10 5966386 5966386 single base substitution C T upstream_gene_variant MELA-AU 10 5966774 5966774 single base substitution C T downstream_gene_variant MELA-AU 10 5966774 5966774 single base substitution C T intron_variant MELA-AU 10 5966774 5966774 single base substitution C T upstream_gene_variant MELA-AU 10 5967123 5967123 single base substitution C T downstream_gene_variant MELA-AU 10 5967123 5967123 single base substitution C T intron_variant MELA-AU 10 5967123 5967123 single base substitution C T upstream_gene_variant MELA-AU 10 5967819 5967819 single base substitution C T downstream_gene_variant MELA-AU 10 5967819 5967819 single base substitution C T intron_variant MELA-AU 10 5968061 5968061 single base substitution A C downstream_gene_variant MELA-AU 10 5968061 5968061 single base substitution A C intron_variant MELA-AU 10 5968261 5968261 single base substitution G A downstream_gene_variant MELA-AU 10 5968261 5968261 single base substitution G A intron_variant MELA-AU 10 5969063 5969063 single base substitution C T downstream_gene_variant MELA-AU 10 5969063 5969063 single base substitution C T intron_variant MELA-AU 10 5969066 5969066 single base substitution C T downstream_gene_variant MELA-AU 10 5969066 5969066 single base substitution C T intron_variant MELA-AU 10 5970781 5970785 deletion of <=200bp TATTT - downstream_gene_variant MELA-AU 10 5970781 5970785 deletion of <=200bp TATTT - intron_variant MELA-AU 10 5972513 5972513 single base substitution C T downstream_gene_variant MELA-AU 10 5972513 5972513 single base substitution C T intron_variant MELA-AU 10 5973350 5973350 single base substitution C T downstream_gene_variant MELA-AU 10 5973350 5973350 single base substitution C T intron_variant MELA-AU 10 5974257 5974257 single base substitution C T downstream_gene_variant MELA-AU 10 5974257 5974257 single base substitution C T intron_variant MELA-AU 10 5974257 5974257 single base substitution C T upstream_gene_variant MELA-AU 10 5975258 5975259 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 5975258 5975259 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 5975258 5975259 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 5976156 5976156 single base substitution C T downstream_gene_variant MELA-AU 10 5976156 5976156 single base substitution C T intron_variant MELA-AU 10 5976156 5976156 single base substitution C T upstream_gene_variant MELA-AU 10 5976195 5976195 single base substitution C T downstream_gene_variant MELA-AU 10 5976195 5976195 single base substitution C T intron_variant MELA-AU 10 5976195 5976195 single base substitution C T upstream_gene_variant MELA-AU 10 5976329 5976329 single base substitution T G downstream_gene_variant MELA-AU 10 5976329 5976329 single base substitution T G intron_variant MELA-AU 10 5976329 5976329 single base substitution T G upstream_gene_variant MELA-AU 10 5976425 5976425 single base substitution C T downstream_gene_variant MELA-AU 10 5976425 5976425 single base substitution C T intron_variant MELA-AU 10 5976425 5976425 single base substitution C T upstream_gene_variant MELA-AU 10 5976908 5976908 single base substitution G A intron_variant MELA-AU 10 5976908 5976908 single base substitution G A upstream_gene_variant MELA-AU 10 5977072 5977072 single base substitution C T intron_variant MELA-AU 10 5977072 5977072 single base substitution C T upstream_gene_variant MELA-AU 10 5977414 5977414 single base substitution T C intron_variant MELA-AU 10 5977414 5977414 single base substitution T C upstream_gene_variant MELA-AU 10 5978304 5978304 single base substitution C T intron_variant MELA-AU 10 5978304 5978304 single base substitution C T upstream_gene_variant MELA-AU 10 5978361 5978361 single base substitution C T intron_variant MELA-AU 10 5978361 5978361 single base substitution C T upstream_gene_variant MELA-AU 10 5979023 5979023 single base substitution C T intron_variant MELA-AU 10 5979147 5979147 single base substitution C T downstream_gene_variant MELA-AU 10 5979147 5979147 single base substitution C T intron_variant MELA-AU 10 5979147 5979147 single base substitution C T synonymous_variant F1012F 3036C>T MELA-AU 10 5979147 5979147 single base substitution C T synonymous_variant F1063F 3189C>T MELA-AU 10 5979147 5979147 single base substitution C T synonymous_variant F516F 1548C>T MELA-AU 10 5979158 5979159 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 5979158 5979159 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 5979158 5979159 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S1016F 3047CC>TT MELA-AU 10 5979158 5979159 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S1067F 3200CC>TT MELA-AU 10 5979158 5979159 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S520F 1559CC>TT MELA-AU 10 5979623 5979623 single base substitution C T downstream_gene_variant MELA-AU 10 5979772 5979772 single base substitution G A downstream_gene_variant MELA-AU 10 5979914 5979914 single base substitution C T downstream_gene_variant MELA-AU 10 5980126 5980126 single base substitution C T downstream_gene_variant MELA-AU 10 5980460 5980460 single base substitution C T downstream_gene_variant MELA-AU 10 5981042 5981042 single base substitution G A downstream_gene_variant MELA-AU 10 5982090 5982090 single base substitution G A downstream_gene_variant MELA-AU 10 5983640 5983640 single base substitution C T downstream_gene_variant MELA-AU 10 5983927 5983928 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 5984149 5984149 single base substitution C T downstream_gene_variant MELA-AU 10 5984208 5984208 single base substitution C T downstream_gene_variant MELA-AU 10 5984217 5984217 single base substitution C T downstream_gene_variant MELA-AU 10 5984298 5984298 single base substitution C T downstream_gene_variant ORCA-IN 10 5941016 5941016 single base substitution C G intron_variant ORCA-IN 10 5941016 5941016 single base substitution C G upstream_gene_variant ORCA-IN 10 5941273 5941273 insertion of <=200bp - T intron_variant ORCA-IN 10 5941273 5941273 insertion of <=200bp - T upstream_gene_variant ORCA-IN 10 5951198 5951198 single base substitution C T 5_prime_UTR_variant ORCA-IN 10 5951198 5951198 single base substitution C T downstream_gene_variant ORCA-IN 10 5951198 5951198 single base substitution C T exon_variant ORCA-IN 10 5951198 5951198 single base substitution C T missense_variant L321F 961C>T ORCA-IN 10 5951198 5951198 single base substitution C T missense_variant L372F 1114C>T ORCA-IN 10 5951198 5951198 single base substitution C T upstream_gene_variant ORCA-IN 10 5964953 5964953 single base substitution C T intron_variant ORCA-IN 10 5964953 5964953 single base substitution C T upstream_gene_variant ORCA-IN 10 5969058 5969058 single base substitution G A downstream_gene_variant ORCA-IN 10 5969058 5969058 single base substitution G A intron_variant ORCA-IN 10 5976326 5976326 deletion of <=200bp G - downstream_gene_variant ORCA-IN 10 5976326 5976326 deletion of <=200bp G - intron_variant ORCA-IN 10 5976326 5976326 deletion of <=200bp G - upstream_gene_variant ORCA-IN 10 5978458 5978458 single base substitution A G exon_variant ORCA-IN 10 5978458 5978458 single base substitution A G missense_variant K1008E 3022A>G ORCA-IN 10 5978458 5978458 single base substitution A G missense_variant K461E 1381A>G ORCA-IN 10 5978458 5978458 single base substitution A G missense_variant K957E 2869A>G ORCA-IN 10 5978458 5978458 single base substitution A G upstream_gene_variant ORCA-IN 10 5978987 5978987 single base substitution C T intron_variant OV-AU 10 5927481 5927481 single base substitution T A upstream_gene_variant OV-AU 10 5935775 5935775 single base substitution A G intron_variant OV-AU 10 5935775 5935775 single base substitution A G upstream_gene_variant OV-AU 10 5939744 5939744 single base substitution C G intron_variant OV-AU 10 5942003 5942003 single base substitution G A intron_variant OV-AU 10 5942003 5942003 single base substitution G A upstream_gene_variant OV-AU 10 5942874 5942874 single base substitution A T intron_variant OV-AU 10 5942874 5942874 single base substitution A T upstream_gene_variant OV-AU 10 5943495 5943495 single base substitution C T intron_variant OV-AU 10 5943495 5943495 single base substitution C T upstream_gene_variant OV-AU 10 5949531 5949531 single base substitution A C downstream_gene_variant OV-AU 10 5949531 5949531 single base substitution A C intron_variant OV-AU 10 5961261 5961261 single base substitution C T downstream_gene_variant OV-AU 10 5961261 5961261 single base substitution C T intron_variant OV-AU 10 5961261 5961261 single base substitution C T upstream_gene_variant OV-AU 10 5968526 5968526 single base substitution C A downstream_gene_variant OV-AU 10 5968526 5968526 single base substitution C A intron_variant OV-AU 10 5968709 5968709 single base substitution T G downstream_gene_variant OV-AU 10 5968709 5968709 single base substitution T G intron_variant OV-AU 10 5975414 5975414 single base substitution T A downstream_gene_variant OV-AU 10 5975414 5975414 single base substitution T A intron_variant OV-AU 10 5975414 5975414 single base substitution T A upstream_gene_variant OV-AU 10 5975699 5975699 single base substitution G T downstream_gene_variant OV-AU 10 5975699 5975699 single base substitution G T intron_variant OV-AU 10 5975699 5975699 single base substitution G T upstream_gene_variant OV-US 10 5958363 5958363 single base substitution A T downstream_gene_variant OV-US 10 5958363 5958363 single base substitution A T missense_variant I578F 1732A>T OV-US 10 5958363 5958363 single base substitution A T missense_variant I629F 1885A>T OV-US 10 5958363 5958363 single base substitution A T missense_variant I65F 193A>T OV-US 10 5958363 5958363 single base substitution A T upstream_gene_variant PACA-AU 10 5930949 5930949 single base substitution C T upstream_gene_variant PACA-AU 10 5931796 5931796 single base substitution G A intron_variant PACA-AU 10 5931796 5931796 single base substitution G A upstream_gene_variant PACA-AU 10 5933574 5933574 insertion of <=200bp - AT intron_variant PACA-AU 10 5933574 5933574 insertion of <=200bp - AT upstream_gene_variant PACA-AU 10 5935819 5935819 single base substitution C T intron_variant PACA-AU 10 5935819 5935819 single base substitution C T upstream_gene_variant PACA-AU 10 5937712 5937712 single base substitution C T intron_variant PACA-AU 10 5938215 5938215 single base substitution T A intron_variant PACA-AU 10 5943147 5943147 single base substitution C A intron_variant PACA-AU 10 5943147 5943147 single base substitution C A upstream_gene_variant PACA-AU 10 5959180 5959180 single base substitution C T downstream_gene_variant PACA-AU 10 5959180 5959180 single base substitution C T exon_variant PACA-AU 10 5959180 5959180 single base substitution C T intron_variant PACA-AU 10 5959180 5959180 single base substitution C T upstream_gene_variant PACA-AU 10 5967369 5967369 single base substitution A G downstream_gene_variant PACA-AU 10 5967369 5967369 single base substitution A G exon_variant PACA-AU 10 5967369 5967369 single base substitution A G missense_variant E383G 1148A>G PACA-AU 10 5967369 5967369 single base substitution A G missense_variant E879G 2636A>G PACA-AU 10 5967369 5967369 single base substitution A G missense_variant E930G 2789A>G PACA-AU 10 5967369 5967369 single base substitution A G upstream_gene_variant PACA-AU 10 5975691 5975691 single base substitution G A downstream_gene_variant PACA-AU 10 5975691 5975691 single base substitution G A intron_variant PACA-AU 10 5975691 5975691 single base substitution G A upstream_gene_variant PACA-AU 10 5979984 5979984 single base substitution C T downstream_gene_variant PACA-AU 10 5980541 5980541 single base substitution T G downstream_gene_variant PACA-CA 10 5926918 5926918 single base substitution T C upstream_gene_variant PACA-CA 10 5930451 5930451 single base substitution A G upstream_gene_variant PACA-CA 10 5932279 5932279 single base substitution C T 5_prime_UTR_variant PACA-CA 10 5932279 5932279 single base substitution C T exon_variant PACA-CA 10 5932279 5932279 single base substitution C T intron_variant PACA-CA 10 5932279 5932279 single base substitution C T upstream_gene_variant PACA-CA 10 5936298 5936298 single base substitution A G intron_variant PACA-CA 10 5936298 5936298 single base substitution A G upstream_gene_variant PACA-CA 10 5937761 5937761 single base substitution A T intron_variant PACA-CA 10 5937826 5937826 single base substitution C T intron_variant PACA-CA 10 5942835 5942835 single base substitution G A intron_variant PACA-CA 10 5942835 5942835 single base substitution G A upstream_gene_variant PACA-CA 10 5947205 5947205 single base substitution C T exon_variant PACA-CA 10 5947205 5947205 single base substitution C T intron_variant PACA-CA 10 5947205 5947205 single base substitution C T upstream_gene_variant PACA-CA 10 5950422 5950422 single base substitution G T downstream_gene_variant PACA-CA 10 5950422 5950422 single base substitution G T intron_variant PACA-CA 10 5953620 5953620 single base substitution C T downstream_gene_variant PACA-CA 10 5953620 5953620 single base substitution C T intron_variant PACA-CA 10 5953620 5953620 single base substitution C T upstream_gene_variant PACA-CA 10 5960787 5960787 single base substitution G T downstream_gene_variant PACA-CA 10 5960787 5960787 single base substitution G T intron_variant PACA-CA 10 5960787 5960787 single base substitution G T upstream_gene_variant PACA-CA 10 5968056 5968061 deletion of <=200bp TTATTA - downstream_gene_variant PACA-CA 10 5968056 5968061 deletion of <=200bp TTATTA - intron_variant PACA-CA 10 5968061 5968061 single base substitution A C downstream_gene_variant PACA-CA 10 5968061 5968061 single base substitution A C intron_variant PACA-CA 10 5969012 5969012 single base substitution T A downstream_gene_variant PACA-CA 10 5969012 5969012 single base substitution T A intron_variant PACA-CA 10 5971244 5971244 single base substitution A G downstream_gene_variant PACA-CA 10 5971244 5971244 single base substitution A G intron_variant PACA-CA 10 5976769 5976769 single base substitution C T downstream_gene_variant PACA-CA 10 5976769 5976769 single base substitution C T intron_variant PACA-CA 10 5976769 5976769 single base substitution C T upstream_gene_variant PACA-CA 10 5980219 5980219 single base substitution G A downstream_gene_variant PACA-CA 10 5983337 5983337 single base substitution A C downstream_gene_variant PACA-CA 10 5983869 5983869 single base substitution T G downstream_gene_variant PACA-CA 10 5983877 5983877 single base substitution G A downstream_gene_variant PACA-CA 10 5984150 5984150 single base substitution C A downstream_gene_variant PAEN-AU 10 5929742 5929742 single base substitution C T upstream_gene_variant PAEN-AU 10 5932100 5932100 single base substitution C T intron_variant PAEN-AU 10 5932100 5932100 single base substitution C T upstream_gene_variant PBCA-DE 10 5949715 5949715 single base substitution G A downstream_gene_variant PBCA-DE 10 5949715 5949715 single base substitution G A intron_variant PBCA-DE 10 5954172 5954172 insertion of <=200bp - AT downstream_gene_variant PBCA-DE 10 5954172 5954172 insertion of <=200bp - AT intron_variant PBCA-DE 10 5954172 5954172 insertion of <=200bp - AT upstream_gene_variant PBCA-DE 10 5954185 5954188 deletion of <=200bp TTTC - downstream_gene_variant PBCA-DE 10 5954185 5954188 deletion of <=200bp TTTC - intron_variant PBCA-DE 10 5954185 5954188 deletion of <=200bp TTTC - upstream_gene_variant PBCA-DE 10 5958536 5958537 deletion of <=200bp AG - downstream_gene_variant PBCA-DE 10 5958536 5958537 deletion of <=200bp AG - intron_variant PBCA-DE 10 5958536 5958537 deletion of <=200bp AG - upstream_gene_variant PBCA-DE 10 5962025 5962025 single base substitution C T downstream_gene_variant PBCA-DE 10 5962025 5962025 single base substitution C T intron_variant PBCA-DE 10 5962025 5962025 single base substitution C T upstream_gene_variant PBCA-DE 10 5982546 5982546 single base substitution G A downstream_gene_variant PRAD-CA 10 5976338 5976338 single base substitution T G downstream_gene_variant PRAD-CA 10 5976338 5976338 single base substitution T G intron_variant PRAD-CA 10 5976338 5976338 single base substitution T G upstream_gene_variant PRAD-CA 10 5976339 5976339 single base substitution G T downstream_gene_variant PRAD-CA 10 5976339 5976339 single base substitution G T intron_variant PRAD-CA 10 5976339 5976339 single base substitution G T upstream_gene_variant PRAD-UK 10 5937305 5937305 single base substitution T G intron_variant PRAD-UK 10 5939169 5939169 single base substitution T C intron_variant PRAD-UK 10 5942621 5942621 single base substitution A T intron_variant PRAD-UK 10 5942621 5942621 single base substitution A T upstream_gene_variant PRAD-UK 10 5946808 5946808 single base substitution T A intron_variant PRAD-UK 10 5946808 5946808 single base substitution T A upstream_gene_variant PRAD-US 10 5948526 5948526 single base substitution G A 5_prime_UTR_variant PRAD-US 10 5948526 5948526 single base substitution G A exon_variant PRAD-US 10 5948526 5948526 single base substitution G A synonymous_variant P228P 684G>A PRAD-US 10 5948526 5948526 single base substitution G A synonymous_variant P279P 837G>A PRAD-US 10 5979235 5979235 single base substitution G A downstream_gene_variant PRAD-US 10 5979235 5979235 single base substitution G A exon_variant PRAD-US 10 5979235 5979235 single base substitution G A missense_variant V1042I 3124G>A PRAD-US 10 5979235 5979235 single base substitution G A missense_variant V1093I 3277G>A PRAD-US 10 5979235 5979235 single base substitution G A missense_variant V546I 1636G>A READ-US 10 5945092 5945092 single base substitution G A 5_prime_UTR_variant READ-US 10 5945092 5945092 single base substitution G A exon_variant READ-US 10 5945092 5945092 single base substitution G A intron_variant READ-US 10 5945092 5945092 single base substitution G A synonymous_variant P37P 111G>A READ-US 10 5945092 5945092 single base substitution G A synonymous_variant P88P 264G>A READ-US 10 5945092 5945092 single base substitution G A upstream_gene_variant READ-US 10 5948296 5948296 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant READ-US 10 5948296 5948296 single base substitution T C exon_variant READ-US 10 5948296 5948296 single base substitution T C synonymous_variant L152L 454T>C READ-US 10 5948296 5948296 single base substitution T C synonymous_variant L203L 607T>C READ-US 10 5948296 5948296 single base substitution T C upstream_gene_variant READ-US 10 5966354 5966354 single base substitution G A exon_variant READ-US 10 5966354 5966354 single base substitution G A missense_variant A314T 940G>A READ-US 10 5966354 5966354 single base substitution G A missense_variant A827T 2479G>A READ-US 10 5966354 5966354 single base substitution G A missense_variant A878T 2632G>A READ-US 10 5966354 5966354 single base substitution G A upstream_gene_variant RECA-EU 10 5934211 5934211 single base substitution T A intron_variant RECA-EU 10 5934211 5934211 single base substitution T A upstream_gene_variant RECA-EU 10 5935891 5935891 single base substitution T G intron_variant RECA-EU 10 5935891 5935891 single base substitution T G upstream_gene_variant RECA-EU 10 5949950 5949950 single base substitution T C downstream_gene_variant RECA-EU 10 5949950 5949950 single base substitution T C intron_variant RECA-EU 10 5970055 5970055 single base substitution A G downstream_gene_variant RECA-EU 10 5970055 5970055 single base substitution A G intron_variant RECA-EU 10 5970288 5970288 single base substitution T A downstream_gene_variant RECA-EU 10 5970288 5970288 single base substitution T A intron_variant RECA-EU 10 5976338 5976338 single base substitution T G downstream_gene_variant RECA-EU 10 5976338 5976338 single base substitution T G intron_variant RECA-EU 10 5976338 5976338 single base substitution T G upstream_gene_variant RECA-EU 10 5977248 5977248 single base substitution G A intron_variant RECA-EU 10 5977248 5977248 single base substitution G A upstream_gene_variant RECA-EU 10 5980039 5980039 single base substitution C T downstream_gene_variant RECA-EU 10 5980427 5980427 single base substitution G A downstream_gene_variant RECA-EU 10 5982703 5982703 single base substitution T G downstream_gene_variant SKCA-BR 10 5929964 5929964 single base substitution G A upstream_gene_variant SKCA-BR 10 5932087 5932087 single base substitution C T intron_variant SKCA-BR 10 5932087 5932087 single base substitution C T upstream_gene_variant SKCA-BR 10 5935168 5935168 single base substitution C T intron_variant SKCA-BR 10 5935168 5935168 single base substitution C T upstream_gene_variant SKCA-BR 10 5942526 5942526 single base substitution G A intron_variant SKCA-BR 10 5942526 5942526 single base substitution G A upstream_gene_variant SKCA-BR 10 5942942 5942942 single base substitution C T intron_variant SKCA-BR 10 5942942 5942942 single base substitution C T upstream_gene_variant SKCA-BR 10 5943364 5943364 single base substitution A C intron_variant SKCA-BR 10 5943364 5943364 single base substitution A C upstream_gene_variant SKCA-BR 10 5943986 5943986 single base substitution G A intron_variant SKCA-BR 10 5943986 5943986 single base substitution G A upstream_gene_variant SKCA-BR 10 5944784 5944784 single base substitution T C intron_variant SKCA-BR 10 5944784 5944784 single base substitution T C upstream_gene_variant SKCA-BR 10 5947685 5947685 single base substitution G T intron_variant SKCA-BR 10 5947685 5947685 single base substitution G T upstream_gene_variant SKCA-BR 10 5949316 5949316 single base substitution C T downstream_gene_variant SKCA-BR 10 5949316 5949316 single base substitution C T intron_variant SKCA-BR 10 5949422 5949425 deletion of <=200bp TTTG - downstream_gene_variant SKCA-BR 10 5949422 5949425 deletion of <=200bp TTTG - intron_variant SKCA-BR 10 5958552 5958552 single base substitution G A downstream_gene_variant SKCA-BR 10 5958552 5958552 single base substitution G A intron_variant SKCA-BR 10 5958552 5958552 single base substitution G A upstream_gene_variant SKCA-BR 10 5958695 5958695 single base substitution C G downstream_gene_variant SKCA-BR 10 5958695 5958695 single base substitution C G intron_variant SKCA-BR 10 5958695 5958695 single base substitution C G upstream_gene_variant SKCA-BR 10 5959190 5959190 single base substitution C T downstream_gene_variant SKCA-BR 10 5959190 5959190 single base substitution C T exon_variant SKCA-BR 10 5959190 5959190 single base substitution C T intron_variant SKCA-BR 10 5959190 5959190 single base substitution C T upstream_gene_variant SKCA-BR 10 5959602 5959602 single base substitution C T downstream_gene_variant SKCA-BR 10 5959602 5959602 single base substitution C T synonymous_variant D129D 387C>T SKCA-BR 10 5959602 5959602 single base substitution C T synonymous_variant D642D 1926C>T SKCA-BR 10 5959602 5959602 single base substitution C T synonymous_variant D693D 2079C>T SKCA-BR 10 5959602 5959602 single base substitution C T upstream_gene_variant SKCA-BR 10 5966535 5966536 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 10 5966535 5966536 deletion of <=200bp CT - intron_variant SKCA-BR 10 5966535 5966536 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 10 5966806 5966806 single base substitution G A downstream_gene_variant SKCA-BR 10 5966806 5966806 single base substitution G A intron_variant SKCA-BR 10 5966806 5966806 single base substitution G A upstream_gene_variant SKCA-BR 10 5967123 5967123 single base substitution C T downstream_gene_variant SKCA-BR 10 5967123 5967123 single base substitution C T intron_variant SKCA-BR 10 5967123 5967123 single base substitution C T upstream_gene_variant SKCA-BR 10 5967176 5967176 single base substitution C T downstream_gene_variant SKCA-BR 10 5967176 5967176 single base substitution C T intron_variant SKCA-BR 10 5967176 5967176 single base substitution C T upstream_gene_variant SKCA-BR 10 5969215 5969215 single base substitution C G downstream_gene_variant SKCA-BR 10 5969215 5969215 single base substitution C G intron_variant SKCA-BR 10 5971452 5971452 single base substitution G A downstream_gene_variant SKCA-BR 10 5971452 5971452 single base substitution G A exon_variant SKCA-BR 10 5971452 5971452 single base substitution G A intron_variant SKCA-BR 10 5971882 5971882 single base substitution G C downstream_gene_variant SKCA-BR 10 5971882 5971882 single base substitution G C intron_variant SKCA-BR 10 5975380 5975381 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 10 5975380 5975381 deletion of <=200bp CT - intron_variant SKCA-BR 10 5975380 5975381 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 10 5976337 5976339 deletion of <=200bp TTG - downstream_gene_variant SKCA-BR 10 5976337 5976339 deletion of <=200bp TTG - intron_variant SKCA-BR 10 5976337 5976339 deletion of <=200bp TTG - upstream_gene_variant SKCA-BR 10 5976578 5976578 single base substitution T G downstream_gene_variant SKCA-BR 10 5976578 5976578 single base substitution T G intron_variant SKCA-BR 10 5976578 5976578 single base substitution T G upstream_gene_variant SKCA-BR 10 5978297 5978297 single base substitution T G intron_variant SKCA-BR 10 5978297 5978297 single base substitution T G upstream_gene_variant SKCA-BR 10 5978332 5978332 single base substitution T G intron_variant SKCA-BR 10 5978332 5978332 single base substitution T G upstream_gene_variant SKCM-US 10 5929972 5929972 single base substitution C T upstream_gene_variant SKCM-US 10 5937086 5937086 single base substitution C T intron_variant SKCM-US 10 5937086 5937086 single base substitution C T synonymous_variant G30G 90C>T SKCM-US 10 5948022 5948022 single base substitution C T 5_prime_UTR_variant SKCM-US 10 5948022 5948022 single base substitution C T exon_variant SKCM-US 10 5948022 5948022 single base substitution C T synonymous_variant I111I 333C>T SKCM-US 10 5948022 5948022 single base substitution C T synonymous_variant I60I 180C>T SKCM-US 10 5948022 5948022 single base substitution C T upstream_gene_variant SKCM-US 10 5948180 5948180 single base substitution C T 5_prime_UTR_variant SKCM-US 10 5948180 5948180 single base substitution C T exon_variant SKCM-US 10 5948180 5948180 single base substitution C T missense_variant S113L 338C>T SKCM-US 10 5948180 5948180 single base substitution C T missense_variant S164L 491C>T SKCM-US 10 5948180 5948180 single base substitution C T upstream_gene_variant SKCM-US 10 5948548 5948548 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 5948548 5948548 single base substitution C T exon_variant SKCM-US 10 5948548 5948548 single base substitution C T synonymous_variant L236L 706C>T SKCM-US 10 5948548 5948548 single base substitution C T synonymous_variant L287L 859C>T SKCM-US 10 5951148 5951148 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 5951148 5951148 single base substitution C T downstream_gene_variant SKCM-US 10 5951148 5951148 single base substitution C T exon_variant SKCM-US 10 5951148 5951148 single base substitution C T missense_variant P304L 911C>T SKCM-US 10 5951148 5951148 single base substitution C T missense_variant P355L 1064C>T SKCM-US 10 5951148 5951148 single base substitution C T upstream_gene_variant SKCM-US 10 5953047 5953047 single base substitution G T 5_prime_UTR_variant SKCM-US 10 5953047 5953047 single base substitution G T downstream_gene_variant SKCM-US 10 5953047 5953047 single base substitution G T synonymous_variant V389V 1167G>T SKCM-US 10 5953047 5953047 single base substitution G T synonymous_variant V440V 1320G>T SKCM-US 10 5953047 5953047 single base substitution G T upstream_gene_variant SKCM-US 10 5958258 5958258 single base substitution C T downstream_gene_variant SKCM-US 10 5958258 5958258 single base substitution C T missense_variant L30F 88C>T SKCM-US 10 5958258 5958258 single base substitution C T missense_variant L543F 1627C>T SKCM-US 10 5958258 5958258 single base substitution C T missense_variant L594F 1780C>T SKCM-US 10 5958258 5958258 single base substitution C T upstream_gene_variant SKCM-US 10 5960343 5960343 single base substitution A C downstream_gene_variant SKCM-US 10 5960343 5960343 single base substitution A C missense_variant I155L 463A>C SKCM-US 10 5960343 5960343 single base substitution A C missense_variant I668L 2002A>C SKCM-US 10 5960343 5960343 single base substitution A C missense_variant I719L 2155A>C SKCM-US 10 5960343 5960343 single base substitution A C upstream_gene_variant SKCM-US 10 5960373 5960373 single base substitution T A downstream_gene_variant SKCM-US 10 5960373 5960373 single base substitution T A missense_variant Y165N 493T>A SKCM-US 10 5960373 5960373 single base substitution T A missense_variant Y678N 2032T>A SKCM-US 10 5960373 5960373 single base substitution T A missense_variant Y729N 2185T>A SKCM-US 10 5960373 5960373 single base substitution T A upstream_gene_variant SKCM-US 10 5963508 5963508 single base substitution C T downstream_gene_variant SKCM-US 10 5963508 5963508 single base substitution C T exon_variant SKCM-US 10 5963508 5963508 single base substitution C T synonymous_variant F253F 759C>T SKCM-US 10 5963508 5963508 single base substitution C T synonymous_variant F766F 2298C>T SKCM-US 10 5963508 5963508 single base substitution C T synonymous_variant F817F 2451C>T SKCM-US 10 5963508 5963508 single base substitution C T upstream_gene_variant SKCM-US 10 5969458 5969458 single base substitution G A downstream_gene_variant SKCM-US 10 5969458 5969458 single base substitution G A exon_variant SKCM-US 10 5969458 5969458 single base substitution G A missense_variant R432H 1295G>A SKCM-US 10 5969458 5969458 single base substitution G A missense_variant R928H 2783G>A SKCM-US 10 5969458 5969458 single base substitution G A missense_variant R979H 2936G>A SKCM-US 10 5979147 5979147 single base substitution C T downstream_gene_variant SKCM-US 10 5979147 5979147 single base substitution C T intron_variant SKCM-US 10 5979147 5979147 single base substitution C T synonymous_variant F1012F 3036C>T SKCM-US 10 5979147 5979147 single base substitution C T synonymous_variant F1063F 3189C>T SKCM-US 10 5979147 5979147 single base substitution C T synonymous_variant F516F 1548C>T SKCM-US 10 5979201 5979201 single base substitution C T downstream_gene_variant SKCM-US 10 5979201 5979201 single base substitution C T exon_variant SKCM-US 10 5979201 5979201 single base substitution C T synonymous_variant I1030I 3090C>T SKCM-US 10 5979201 5979201 single base substitution C T synonymous_variant I1081I 3243C>T SKCM-US 10 5979201 5979201 single base substitution C T synonymous_variant I534I 1602C>T STAD-US 10 5948257 5948257 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 10 5948257 5948257 single base substitution C T exon_variant STAD-US 10 5948257 5948257 single base substitution C T missense_variant R139W 415C>T STAD-US 10 5948257 5948257 single base substitution C T missense_variant R190W 568C>T STAD-US 10 5948257 5948257 single base substitution C T upstream_gene_variant STAD-US 10 5951237 5951237 single base substitution G A 5_prime_UTR_variant STAD-US 10 5951237 5951237 single base substitution G A downstream_gene_variant STAD-US 10 5951237 5951237 single base substitution G A exon_variant STAD-US 10 5951237 5951237 single base substitution G A missense_variant D334N 1000G>A STAD-US 10 5951237 5951237 single base substitution G A missense_variant D385N 1153G>A STAD-US 10 5951237 5951237 single base substitution G A upstream_gene_variant STAD-US 10 5952995 5952995 single base substitution G A 5_prime_UTR_variant STAD-US 10 5952995 5952995 single base substitution G A downstream_gene_variant STAD-US 10 5952995 5952995 single base substitution G A missense_variant S372N 1115G>A STAD-US 10 5952995 5952995 single base substitution G A missense_variant S423N 1268G>A STAD-US 10 5952995 5952995 single base substitution G A upstream_gene_variant STAD-US 10 5955763 5955763 single base substitution A G 5_prime_UTR_variant STAD-US 10 5955763 5955763 single base substitution A G downstream_gene_variant STAD-US 10 5955763 5955763 single base substitution A G missense_variant Q422R 1265A>G STAD-US 10 5955763 5955763 single base substitution A G missense_variant Q473R 1418A>G STAD-US 10 5955763 5955763 single base substitution A G upstream_gene_variant STAD-US 10 5956183 5956183 single base substitution G A 5_prime_UTR_variant STAD-US 10 5956183 5956183 single base substitution G A downstream_gene_variant STAD-US 10 5956183 5956183 single base substitution G A exon_variant STAD-US 10 5956183 5956183 single base substitution G A synonymous_variant L449L 1347G>A STAD-US 10 5956183 5956183 single base substitution G A synonymous_variant L500L 1500G>A STAD-US 10 5956183 5956183 single base substitution G A upstream_gene_variant STAD-US 10 5957404 5957404 single base substitution A C 5_prime_UTR_variant STAD-US 10 5957404 5957404 single base substitution A C downstream_gene_variant STAD-US 10 5957404 5957404 single base substitution A C exon_variant STAD-US 10 5957404 5957404 single base substitution A C missense_variant K479Q 1435A>C STAD-US 10 5957404 5957404 single base substitution A C missense_variant K530Q 1588A>C STAD-US 10 5957404 5957404 single base substitution A C upstream_gene_variant STAD-US 10 5957467 5957467 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 10 5957467 5957467 single base substitution C T downstream_gene_variant STAD-US 10 5957467 5957467 single base substitution C T exon_variant STAD-US 10 5957467 5957467 single base substitution C T missense_variant R500C 1498C>T STAD-US 10 5957467 5957467 single base substitution C T missense_variant R551C 1651C>T STAD-US 10 5957467 5957467 single base substitution C T upstream_gene_variant STAD-US 10 5959450 5959450 single base substitution C T downstream_gene_variant STAD-US 10 5959450 5959450 single base substitution C T exon_variant STAD-US 10 5959450 5959450 single base substitution C T missense_variant A106V 317C>T STAD-US 10 5959450 5959450 single base substitution C T missense_variant A619V 1856C>T STAD-US 10 5959450 5959450 single base substitution C T missense_variant A670V 2009C>T STAD-US 10 5959450 5959450 single base substitution C T upstream_gene_variant STAD-US 10 5963252 5963252 single base substitution T C downstream_gene_variant STAD-US 10 5963252 5963252 single base substitution T C missense_variant V198A 593T>C STAD-US 10 5963252 5963252 single base substitution T C missense_variant V711A 2132T>C STAD-US 10 5963252 5963252 single base substitution T C missense_variant V762A 2285T>C STAD-US 10 5963252 5963252 single base substitution T C upstream_gene_variant STAD-US 10 5966439 5966439 deletion of <=200bp A - downstream_gene_variant STAD-US 10 5966439 5966439 deletion of <=200bp A - exon_variant STAD-US 10 5966439 5966439 deletion of <=200bp A - frameshift_variant E342 STAD-US 10 5966439 5966439 deletion of <=200bp A - frameshift_variant E855 STAD-US 10 5966439 5966439 deletion of <=200bp A - frameshift_variant E906 STAD-US 10 5966439 5966439 deletion of <=200bp A - upstream_gene_variant STAD-US 10 5966457 5966457 single base substitution A T downstream_gene_variant STAD-US 10 5966457 5966457 single base substitution A T exon_variant STAD-US 10 5966457 5966457 single base substitution A T missense_variant D348V 1043A>T STAD-US 10 5966457 5966457 single base substitution A T missense_variant D861V 2582A>T STAD-US 10 5966457 5966457 single base substitution A T missense_variant D912V 2735A>T STAD-US 10 5966457 5966457 single base substitution A T upstream_gene_variant STAD-US 10 5978466 5978466 single base substitution C T exon_variant STAD-US 10 5978466 5978466 single base substitution C T synonymous_variant G1010G 3030C>T STAD-US 10 5978466 5978466 single base substitution C T synonymous_variant G463G 1389C>T STAD-US 10 5978466 5978466 single base substitution C T synonymous_variant G959G 2877C>T STAD-US 10 5978466 5978466 single base substitution C T upstream_gene_variant THCA-US 10 5948520 5948520 single base substitution C T 5_prime_UTR_variant THCA-US 10 5948520 5948520 single base substitution C T exon_variant THCA-US 10 5948520 5948520 single base substitution C T synonymous_variant F226F 678C>T THCA-US 10 5948520 5948520 single base substitution C T synonymous_variant F277F 831C>T UCEC-US 10 5929946 5929946 single base substitution C A upstream_gene_variant UCEC-US 10 5937150 5937150 single base substitution A C intron_variant UCEC-US 10 5937150 5937150 single base substitution A C missense_variant M52L 154A>C UCEC-US 10 5948196 5948196 single base substitution G A 5_prime_UTR_variant UCEC-US 10 5948196 5948196 single base substitution G A exon_variant UCEC-US 10 5948196 5948196 single base substitution G A synonymous_variant P118P 354G>A UCEC-US 10 5948196 5948196 single base substitution G A synonymous_variant P169P 507G>A UCEC-US 10 5948196 5948196 single base substitution G A upstream_gene_variant UCEC-US 10 5948281 5948281 single base substitution G A 5_prime_UTR_variant UCEC-US 10 5948281 5948281 single base substitution G A exon_variant UCEC-US 10 5948281 5948281 single base substitution G A missense_variant A147T 439G>A UCEC-US 10 5948281 5948281 single base substitution G A missense_variant A198T 592G>A UCEC-US 10 5948281 5948281 single base substitution G A upstream_gene_variant UCEC-US 10 5948287 5948287 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 5948287 5948287 single base substitution C T exon_variant UCEC-US 10 5948287 5948287 single base substitution C T missense_variant R149W 445C>T UCEC-US 10 5948287 5948287 single base substitution C T missense_variant R200W 598C>T UCEC-US 10 5948287 5948287 single base substitution C T upstream_gene_variant UCEC-US 10 5948509 5948509 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 5948509 5948509 single base substitution G A exon_variant UCEC-US 10 5948509 5948509 single base substitution G A missense_variant V223M 667G>A UCEC-US 10 5948509 5948509 single base substitution G A missense_variant V274M 820G>A UCEC-US 10 5957433 5957433 single base substitution G T 5_prime_UTR_variant UCEC-US 10 5957433 5957433 single base substitution G T downstream_gene_variant UCEC-US 10 5957433 5957433 single base substitution G T exon_variant UCEC-US 10 5957433 5957433 single base substitution G T synonymous_variant V488V 1464G>T UCEC-US 10 5957433 5957433 single base substitution G T synonymous_variant V539V 1617G>T UCEC-US 10 5957433 5957433 single base substitution G T upstream_gene_variant UCEC-US 10 5957464 5957464 single base substitution G A 5_prime_UTR_variant UCEC-US 10 5957464 5957464 single base substitution G A downstream_gene_variant UCEC-US 10 5957464 5957464 single base substitution G A exon_variant UCEC-US 10 5957464 5957464 single base substitution G A missense_variant E499K 1495G>A UCEC-US 10 5957464 5957464 single base substitution G A missense_variant E550K 1648G>A UCEC-US 10 5957464 5957464 single base substitution G A upstream_gene_variant UCEC-US 10 5957517 5957517 single base substitution C T downstream_gene_variant UCEC-US 10 5957517 5957517 single base substitution C T exon_variant UCEC-US 10 5957517 5957517 single base substitution C T synonymous_variant Y3Y 9C>T UCEC-US 10 5957517 5957517 single base substitution C T synonymous_variant Y516Y 1548C>T UCEC-US 10 5957517 5957517 single base substitution C T synonymous_variant Y567Y 1701C>T UCEC-US 10 5957517 5957517 single base substitution C T upstream_gene_variant UCEC-US 10 5958395 5958395 single base substitution C A downstream_gene_variant UCEC-US 10 5958395 5958395 single base substitution C A synonymous_variant V588V 1764C>A UCEC-US 10 5958395 5958395 single base substitution C A synonymous_variant V639V 1917C>A UCEC-US 10 5958395 5958395 single base substitution C A synonymous_variant V75V 225C>A UCEC-US 10 5958395 5958395 single base substitution C A upstream_gene_variant UCEC-US 10 5960424 5960424 single base substitution G A downstream_gene_variant UCEC-US 10 5960424 5960424 single base substitution G A missense_variant V182I 544G>A UCEC-US 10 5960424 5960424 single base substitution G A missense_variant V695I 2083G>A UCEC-US 10 5960424 5960424 single base substitution G A missense_variant V746I 2236G>A UCEC-US 10 5960424 5960424 single base substitution G A upstream_gene_variant UCEC-US 10 5967362 5967362 single base substitution G T downstream_gene_variant UCEC-US 10 5967362 5967362 single base substitution G T exon_variant UCEC-US 10 5967362 5967362 single base substitution G T missense_variant G381C 1141G>T UCEC-US 10 5967362 5967362 single base substitution G T missense_variant G877C 2629G>T UCEC-US 10 5967362 5967362 single base substitution G T missense_variant G928C 2782G>T UCEC-US 10 5967362 5967362 single base substitution G T upstream_gene_variant UCEC-US 10 5969446 5969446 single base substitution G A downstream_gene_variant UCEC-US 10 5969446 5969446 single base substitution G A exon_variant UCEC-US 10 5969446 5969446 single base substitution G A missense_variant R428Q 1283G>A UCEC-US 10 5969446 5969446 single base substitution G A missense_variant R924Q 2771G>A UCEC-US 10 5969446 5969446 single base substitution G A missense_variant R975Q 2924G>A UCEC-US 10 5979174 5979174 single base substitution C T downstream_gene_variant UCEC-US 10 5979174 5979174 single base substitution C T exon_variant UCEC-US 10 5979174 5979174 single base substitution C T synonymous_variant R1021R 3063C>T UCEC-US 10 5979174 5979174 single base substitution C T synonymous_variant R1072R 3216C>T UCEC-US 10 5979174 5979174 single base substitution C T synonymous_variant R525R 1575C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-B8-4148-01 COSM465783 c.1058G>A p.C353Y Substitution - Missense 10:5909179-5909179 + CSCC-31-T COSM4477854 c.2190C>A p.T730T Substitution - coding silent 10:5918415-5918415 + PD4956a COSM5788019 c.1744C>G p.L582V Substitution - Missense 10:5916259-5916259 + TCGA-EK-A2RO-01 COSM427713 c.241C>T p.Q81* Substitution - Nonsense 10:5903106-5903106 + CSCC-49-T COSM4472159 c.1764C>T p.F588F Substitution - coding silent 10:5916279-5916279 + S02299 COSM5689983 c.378G>T p.M126I Substitution - Missense 10:5906104-5906104 + PD8978a COSM919128 c.598C>T p.R200W Substitution - Missense 10:5906324-5906324 + HCC2998 COSM2148037 c.264G>A p.P88P Substitution - coding silent 10:5903129-5903129 + TCGA-CJ-4895-01 COSM3358787 c.2317G>A p.V773I Substitution - Missense 10:5921321-5921321 + LUAD-RT-S01477 COSM377390 c.837G>A p.P279P Substitution - coding silent 10:5906563-5906563 + TCGA-GN-A26C-01 COSM3439069 c.859C>T p.L287L Substitution - coding silent 10:5906585-5906585 + TCGA-BR-7707-01 COSM4014830 c.568C>T p.R190W Substitution - Missense 10:5906294-5906294 + TCGA-BR-8686-01 COSM4014833 c.1500G>A p.L500L Substitution - coding silent 10:5914220-5914220 + TCGA-BS-A0UV-01 COSM919136 c.2924G>A p.R975Q Substitution - Missense 10:5927483-5927483 + PTC-14C COSM4144766 c.2743T>A p.F915I Substitution - Missense 10:5924502-5924502 + T3225 COSM4683929 c.1964G>A p.R655H Substitution - Missense 10:5917442-5917442 + MZ7-mel COSM25629 c.2092G>A p.D698N Substitution - Missense 10:5917652-5917652 + HT115 COSM2148032 c.88G>A p.G30S Substitution - Missense 10:5895121-5895121 + TCGA-AA-A010-01 COSM281090 c.2951A>C p.K984T Substitution - Missense 10:5927510-5927510 + PD6404a COSM4014839 c.3030C>T p.G1010G Substitution - coding silent 10:5936503-5936503 + LUAD-S01306 COSM343405 c.1122G>T p.E374D Substitution - Missense 10:5909243-5909243 + 2492723 COSM5723415 c.2762G>C p.G921A Substitution - Missense 10:5925379-5925379 + CSCC-35-T COSM4514286 c.96C>T p.L32L Substitution - coding silent 10:5895129-5895129 + TCGA-AA-A010-01 COSM281089 c.1199C>T p.A400V Substitution - Missense 10:5910963-5910963 + HCC2998 COSM2148056 c.1153G>A p.D385N Substitution - Missense 10:5909274-5909274 + TCGA-BH-A0HB-01 COSM427715 c.2254-1G>T p.? Unknown 10:5921257-5921257 + PT48 COSM5932614 c.232C>T p.P78S Substitution - Missense 10:5903097-5903097 + TCGA-HG-A2PA-01 COSM4823580 c.1560G>A p.K520K Substitution - coding silent 10:5915413-5915413 + TCGA-A8-A0A9-01 COSM427713 c.241C>T p.Q81* Substitution - Nonsense 10:5903106-5903106 + 446 COSM4434923 c.1668C>T p.N556N Substitution - coding silent 10:5915521-5915521 + TCGA-AX-A05Z-01 COSM919133 c.1917C>A p.V639V Substitution - coding silent 10:5916432-5916432 + TCGA-13-0890-01 COSM74631 c.1885A>T p.I629F Substitution - Missense 10:5916400-5916400 + TCGA-AA-3821-01 COSM294370 c.148delG p.A50fs*3 Deletion - Frameshift 10:5895181-5895181 + CRC-19T COSM5480782 c.3109A>G p.T1037A Substitution - Missense 10:5936582-5936582 + ESO-005 COSM1252259 c.2406C>T p.N802N Substitution - coding silent 10:5921500-5921500 + Pat_01_A COSM2148050 c.836C>T p.P279L Substitution - Missense 10:5906562-5906562 + ESO-717 COSM1242271 c.188T>C p.I63T Substitution - Missense 10:5903053-5903053 + ccRCC-15 COSM1661819 c.433A>G p.I145V Substitution - Missense 10:5906159-5906159 + TCGA-23-1122-01 COSM70753 c.2983G>C p.E995Q Substitution - Missense 10:5936456-5936456 + pfg008T COSM4014832 c.1418A>G p.Q473R Substitution - Missense 10:5913800-5913800 + PT08_2 COSM5893465 c.763C>T p.P255S Substitution - Missense 10:5906489-5906489 + TCGA-HT-7692-01 COSM2148090 c.3170G>A p.R1057H Substitution - Missense 10:5937165-5937165 + YUWIA COSM5370872 c.3202C>T p.P1068S Substitution - Missense 10:5937197-5937197 + S02398 COSM5699574 c.698A>G p.Q233R Substitution - Missense 10:5906424-5906424 + STC243 COSM5050249 c.2856G>A p.Q952Q Substitution - coding silent 10:5925473-5925473 + TCGA-AA-3715-01 COSM269157 c.809T>A p.V270D Substitution - Missense 10:5906535-5906535 + 122-06-01TD COSM5418667 c.2842C>T p.H948Y Substitution - Missense 10:5925459-5925459 + PD7436a COSM3720205 c.2921C>G p.T974S Substitution - Missense 10:5927480-5927480 + TCGA-B6-A0X7-01 COSM427711 c.121G>T p.A41S Substitution - Missense 10:5895154-5895154 + T3658 COSM4683930 c.2116+2T>C p.? Unknown 10:5917678-5917678 + TCGA-AX-A0J1-01 COSM919126 c.507G>A p.P169P Substitution - coding silent 10:5906233-5906233 + RKO COSM2148052 c.1018T>C p.C340R Substitution - Missense 10:5909036-5909036 + T2769 COSM919129 c.820G>A p.V274M Substitution - Missense 10:5906546-5906546 + LIM1215 COSM4639304 c.288G>A p.P96P Substitution - coding silent 10:5903153-5903153 + T1180 COSM4683932 c.2460G>A p.R820R Substitution - coding silent 10:5921554-5921554 + PD4204a COSM161012 c.2055C>T p.S685S Substitution - coding silent 10:5917615-5917615 + PD4204a COSM161011 c.2054G>T p.S685I Substitution - Missense 10:5917614-5917614 + 587224 COSM1206804 c.2740G>A p.D914N Substitution - Missense 10:5924499-5924499 + TCGA-EJ-5510-01 COSM325330 c.3277G>A p.V1093I Substitution - Missense 10:5937272-5937272 + LIM2405 COSM4613221 c.2472_2473insG p.I827fs*2 Insertion - Frameshift 10:5921566-5921567 + pfg205T COSM4749250 c.1346G>A p.G449E Substitution - Missense 10:5911110-5911110 + TCGA-BR-4361-01 COSM4014837 c.2285T>C p.V762A Substitution - Missense 10:5921289-5921289 + 3N45-VS-3T45 COSM4982373 c.2440G>A p.E814K Substitution - Missense 10:5921534-5921534 + Pat_28_B COSM5837053 c.886G>A p.E296K Substitution - Missense 10:5906612-5906612 + TCGA-B5-A11E-01 COSM919137 c.3216C>T p.R1072R Substitution - coding silent 10:5937211-5937211 + TCGA-EE-A181-06 COSM3439074 c.2451C>T p.F817F Substitution - coding silent 10:5921545-5921545 + GC8_T COSM146872 c.3006G>A p.L1002L Substitution - coding silent 10:5936479-5936479 + CSCC-55-T COSM4523930 c.1241G>A p.R414Q Substitution - Missense 10:5911005-5911005 + LUAD-NYU315 COSM373527 c.1098G>C p.L366L Substitution - coding silent 10:5909219-5909219 + TCGA-HT-7480-01 COSM3967100 c.838G>T p.V280L Substitution - Missense 10:5906564-5906564 + C086 COSM5531103 c.3069C>T p.I1023I Substitution - coding silent 10:5936542-5936542 + 587376 COSM1206806 c.1535T>G p.I512S Substitution - Missense 10:5914255-5914255 + RK121_C01 COSM3738661 c.1478C>A p.T493K Substitution - Missense 10:5914198-5914198 + TCGA-F5-6814-01 COSM2148037 c.264G>A p.P88P Substitution - coding silent 10:5903129-5903129 + HCC98 COSM1603572 c.2119A>G p.I707V Substitution - Missense 10:5918344-5918344 + HCC98T COSM1603572 c.2119A>G p.I707V Substitution - Missense 10:5918344-5918344 + 585267 COSM325330 c.3277G>A p.V1093I Substitution - Missense 10:5937272-5937272 + TCGA-CH-5754-01 COSM377390 c.837G>A p.P279P Substitution - coding silent 10:5906563-5906563 + H441 COSM1193638 c.879G>T p.L293F Substitution - Missense 10:5906605-5906605 + TCGA-G4-6302-01 COSM3686792 c.1276G>A p.V426M Substitution - Missense 10:5911040-5911040 + PT48 COSM5932613 c.3070C>T p.P1024S Substitution - Missense 10:5936543-5936543 + TCGA-EE-A2GE-06 COSM3439072 c.1780C>T p.L594F Substitution - Missense 10:5916295-5916295 + TCGA-DK-A3IT-01 COSM1297329 c.237C>A p.F79L Substitution - Missense 10:5903102-5903102 + PD4127a COSM161010 c.2029+5G>C p.? Unknown 10:5917512-5917512 + TCGA-BH-A0C1-01 COSM427712 c.225G>A p.V75V Substitution - coding silent 10:5903090-5903090 + NCI-H727 COSM2148074 c.2029G>T p.G677C Substitution - Missense 10:5917507-5917507 + ME044T COSM229140 c.2530C>T p.P844S Substitution - Missense 10:5923675-5923675 + TCGA-66-2767-01 COSM684838 c.3185C>A p.A1062E Substitution - Missense 10:5937180-5937180 + SNUH_G76_S1 COSM4416822 c.3159T>C p.C1053C Substitution - coding silent 10:5937154-5937154 + 2521262 COSM5892074 c.32G>A p.W11* Substitution - Nonsense 10:5895065-5895065 + TCGA-D8-A1Y3-01 COSM1474679 c.1037G>A p.R346Q Substitution - Missense 10:5909055-5909055 + TCGA-AP-A0LM-01 COSM919135 c.2782G>T p.G928C Substitution - Missense 10:5925399-5925399 + 46M COSM5587796 c.22+2C>A p.? Unknown 10:5894513-5894513 + RK194_C01 COSM1627552 c.1503T>A p.N501K Substitution - Missense 10:5914223-5914223 + TCGA-EE-A2MR-06 COSM3439070 c.1064C>T p.P355L Substitution - Missense 10:5909185-5909185 + TCGA-FS-A1ZA-06 COSM3439073 c.2185T>A p.Y729N Substitution - Missense 10:5918410-5918410 + sysucc-1370T COSM5469425 c.1037+1G>A p.? Unknown 10:5909056-5909056 + TCGA-AA-3715-01 COSM269156 c.720T>C p.P240P Substitution - coding silent 10:5906446-5906446 + Gp2D COSM2148094 c.3215G>A p.R1072H Substitution - Missense 10:5937210-5937210 + CH-103-T2 COSM5650422 c.282T>C p.P94P Substitution - coding silent 10:5903147-5903147 + EGC8 COSM5050248 c.836C>A p.P279Q Substitution - Missense 10:5906562-5906562 + Pat_01_B COSM2148050 c.836C>T p.P279L Substitution - Missense 10:5906562-5906562 + TCGA-AN-A0FX-01 COSM5831483 c.474delC p.S159fs*102 Deletion - Frameshift 10:5906200-5906200 + TCGA-AA-3663-01 COSM1348374 c.3200delC p.P1068fs*>27 Deletion - Frameshift 10:5937195-5937195 + TCGA-HU-A4GT-01 COSM4014832 c.1418A>G p.Q473R Substitution - Missense 10:5913800-5913800 + ESO-081 COSM1243260 c.753T>C p.L251L Substitution - coding silent 10:5906479-5906479 + TCGA-AN-A0AR-01 COSM427714 c.1149C>A p.L383L Substitution - coding silent 10:5909270-5909270 + KM12 COSM2148071 c.1965C>T p.R655R Substitution - coding silent 10:5917443-5917443 + TCGA-BR-8589-01 COSM4014834 c.1588A>C p.K530Q Substitution - Missense 10:5915441-5915441 + CSCC-10-T COSM4499828 c.550C>T p.Q184* Substitution - Nonsense 10:5906276-5906276 + SWE-4C COSM1179583 c.2260C>T p.R754W Substitution - Missense 10:5921264-5921264 + CHC892T COSM4959682 c.2547G>A p.R849R Substitution - coding silent 10:5923692-5923692 + S02139 COSM5674002 c.2389T>A p.L797M Substitution - Missense 10:5921483-5921483 + LUAD-RT-S01477 COSM377391 c.1363A>C p.R455R Substitution - coding silent 10:5911127-5911127 + TCGA-AX-A0J0-01 COSM919130 c.1617G>T p.V539V Substitution - coding silent 10:5915470-5915470 + CHC892T COSM4798038 c.1870A>G p.I624V Substitution - Missense 10:5916385-5916385 + HT115 COSM2148041 c.483G>A p.G161G Substitution - coding silent 10:5906209-5906209 + OSCC-GB_00410111 COSM3709873 c.1114C>T p.L372F Substitution - Missense 10:5909235-5909235 + KM12 COSM2148046 c.706G>A p.G236R Substitution - Missense 10:5906432-5906432 + ESCC-010T COSM3935103 c.1575C>G p.V525V Substitution - coding silent 10:5915428-5915428 + 587256 COSM325330 c.3277G>A p.V1093I Substitution - Missense 10:5937272-5937272 + PT38 COSM5922814 c.913C>T p.P305S Substitution - Missense 10:5908931-5908931 + TCGA-BR-A4J7-01 COSM4014839 c.3030C>T p.G1010G Substitution - coding silent 10:5936503-5936503 + TCGA-DE-A0Y2-01 COSM3368069 c.831C>T p.F277F Substitution - coding silent 10:5906557-5906557 + TCGA-B7-5816-01 COSM4014835 c.1651C>T p.R551C Substitution - Missense 10:5915504-5915504 + TCGA-BP-5199-01 COSM465781 c.79G>T p.G27W Substitution - Missense 10:5895112-5895112 + SJERG021891_D1 COSM4994367 c.2324A>G p.K775R Substitution - Missense 10:5921328-5921328 + HCT116 COSM2148093 c.3185C>T p.A1062V Substitution - Missense 10:5937180-5937180 + TCGA-HU-A4GQ-01 COSM4014838 c.2735A>T p.D912V Substitution - Missense 10:5924494-5924494 + Pat_66_A COSM5837055 c.2431C>T p.R811W Substitution - Missense 10:5921525-5921525 + TCGA-D3-A3MR-06 COSM3439066 c.90C>T p.G30G Substitution - coding silent 10:5895123-5895123 + TCGA-HU-A4GU-01 COSM4014836 c.2009C>T p.A670V Substitution - Missense 10:5917487-5917487 + TCGA-EJ-7125-01 COSM3670563 c.3081C>A p.T1027T Substitution - coding silent 10:5936554-5936554 + TCGA-D8-A1JA-01 COSM3807381 c.2943C>G p.I981M Substitution - Missense 10:5927502-5927502 + TCGA-EI-6882-01 COSM3415122 c.607T>C p.L203L Substitution - coding silent 10:5906333-5906333 + SNUH_G10_S1 COSM3998036 c.1037+7T>C p.? Unknown 10:5909062-5909062 + CSCC-54-T COSM4500422 c.564C>T p.T188T Substitution - coding silent 10:5906290-5906290 + Pat_22_B COSM5837054 c.1798G>A p.G600R Substitution - Missense 10:5916313-5916313 + T2197 COSM4683927 c.298_299delAG p.G101fs*2 Deletion - Frameshift 10:5903163-5903164 + T2269 COSM4683928 c.1560G>T p.K520N Substitution - Missense 10:5915413-5915413 + CRC-06T COSM5456023 c.1329C>T p.Y443Y Substitution - coding silent 10:5911093-5911093 + CSCC-47-T COSM4494769 c.439C>T p.P147S Substitution - Missense 10:5906165-5906165 + TCGA-AA-3666-01 COSM265802 c.1474C>G p.L492V Substitution - Missense 10:5914194-5914194 + RK193_C01 COSM3686968 c.3016G>A p.V1006I Substitution - Missense 10:5936489-5936489 + TCGA-EK-A3GM-01 COSM179352 c.2427C>T p.A809A Substitution - coding silent 10:5921521-5921521 + OSCC-GB_00770111 COSM4884029 c.3022A>G p.K1008E Substitution - Missense 10:5936495-5936495 + TCGA-B0-4823-01 COSM465782 c.477T>C p.S159S Substitution - coding silent 10:5906203-5906203 + LIM1899 COSM4639677 c.977G>A p.G326D Substitution - Missense 10:5908995-5908995 + 41T COSM3709873 c.1114C>T p.L372F Substitution - Missense 10:5909235-5909235 + TCGA-DM-A28K-01 COSM1348368 c.667C>T p.R223W Substitution - Missense 10:5906393-5906393 + ESO-0176 COSM1252260 c.3169C>A p.R1057S Substitution - Missense 10:5937164-5937164 + CSCC-55-T COSM4533910 c.2029G>A p.G677S Substitution - Missense 10:5917507-5917507 + 8057559 COSM3382933 c.2789A>G p.E930G Substitution - Missense 10:5925406-5925406 + TCGA-GV-A3QI-01 COSM1297330 c.1120G>A p.E374K Substitution - Missense 10:5909241-5909241 + TCGA-A5-A0VP-01 COSM919128 c.598C>T p.R200W Substitution - Missense 10:5906324-5906324 + T3024 COSM4683931 c.2323delA p.K776fs*37 Deletion - Frameshift 10:5921327-5921327 + 37 COSM3721795 c.934C>T p.R312* Substitution - Nonsense 10:5908952-5908952 + 384 COSM4426734 c.234C>G p.P78P Substitution - coding silent 10:5903099-5903099 + TCGA-DA-A3F5-06 COSM3439071 c.1320G>T p.V440V Substitution - coding silent 10:5911084-5911084 + SNU-175 COSM2148084 c.2432G>A p.R811Q Substitution - Missense 10:5921526-5921526 + TCGA-AP-A056-01 COSM919125 c.154A>C p.M52L Substitution - Missense 10:5895187-5895187 + ZZUFHECRKL-G051T COSM5431192 c.40C>T p.Q14* Substitution - Nonsense 10:5895073-5895073 + PD4956a COSM5787971 c.1091G>A p.W364* Substitution - Nonsense 10:5909212-5909212 + TCGA-CA-6717-01 COSM1348369 c.1961G>A p.S654N Substitution - Missense 10:5917439-5917439 + PT08_1 COSM5893465 c.763C>T p.P255S Substitution - Missense 10:5906489-5906489 + J80_T COSM3978669 c.109C>T p.Q37* Substitution - Nonsense 10:5895142-5895142 + 587376 COSM1206807 c.2966T>G p.I989S Substitution - Missense 10:5927525-5927525 + SJHGG109_A COSM4971901 c.1574T>C p.V525A Substitution - Missense 10:5915427-5915427 + cSCCP4 COSM143549 c.2188_2189AC>TT p.T730F Substitution - Missense 10:5918413-5918414 + TCGA-BS-A0UV-01 COSM919131 c.1648G>A p.E550K Substitution - Missense 10:5915501-5915501 + CSCC-37-T COSM4521219 c.10G>A p.E4K Substitution - Missense 10:5894499-5894499 + 395 COSM4428615 c.1598_1599delAG p.S534fs*62 Deletion - Frameshift 10:5915451-5915452 + TCGA-KR-A7K8-01 COSM4918230 c.289A>T p.R97* Substitution - Nonsense 10:5903154-5903154 + TCGA-D9-A6EC-06 COSM4401111 c.2155A>C p.I719L Substitution - Missense 10:5918380-5918380 + TCGA-A5-A0VP-01 COSM919134 c.2236G>A p.V746I Substitution - Missense 10:5918461-5918461 + TCGA-AA-A010-01 COSM299216 c.2552-8C>A p.? Unknown 10:5924303-5924303 + TCGA-D3-A3C8-06 COSM3439067 c.333C>T p.I111I Substitution - coding silent 10:5906059-5906059 + ICC009T COSM5823502 c.2131G>A p.V711I Substitution - Missense 10:5918356-5918356 + LUAD-S01409 COSM346267 c.2413G>T p.V805L Substitution - Missense 10:5921507-5921507 + TCGA-43-6770-01 COSM684840 c.450C>T p.S150S Substitution - coding silent 10:5906176-5906176 + YUKARN COSM1686110 c.2936G>A p.R979H Substitution - Missense 10:5927495-5927495 + LUAD-B00523 COSM331684 c.1603A>T p.R535W Substitution - Missense 10:5915456-5915456 + TCGA-24-1847-01 COSM1321285 c.643C>T p.Q215* Substitution - Nonsense 10:5906369-5906369 + TCGA-LL-A441-01 COSM5831482 c.250_253delACAA p.N85fs*31 Deletion - Frameshift 10:5903115-5903118 + TCGA-AP-A0LM-01 COSM919129 c.820G>A p.V274M Substitution - Missense 10:5906546-5906546 + TCGA-AA-3939-01 COSM296686 c.2370C>T p.D790D Substitution - coding silent 10:5921464-5921464 + TCGA-AA-3713-01 COSM1348370 c.2208C>T p.N736N Substitution - coding silent 10:5918433-5918433 + YURDE COSM1686110 c.2936G>A p.R979H Substitution - Missense 10:5927495-5927495 + TCGA-A2-A0T5-01 COSM3807380 c.562A>C p.T188P Substitution - Missense 10:5906288-5906288 + LUAD-RT-S01711 COSM380076 c.2935C>T p.R979C Substitution - Missense 10:5927494-5927494 + TCGA-DA-A3F5-06 COSM1686110 c.2936G>A p.R979H Substitution - Missense 10:5927495-5927495 + TCGA-HU-8602-01 COSM2148056 c.1153G>A p.D385N Substitution - Missense 10:5909274-5909274 + KPOPBR-03-T COSM5965648 c.1521C>G p.L507L Substitution - coding silent 10:5914241-5914241 + T263 COSM4441591 c.1636G>A p.A546T Substitution - Missense 10:5915489-5915489 + C391 COSM4441591 c.1636G>A p.A546T Substitution - Missense 10:5915489-5915489 + BD121T COSM5515310 c.1587G>T p.E529D Substitution - Missense 10:5915440-5915440 + SNU-C4 COSM4651804 c.1831C>T p.L611L Substitution - coding silent 10:5916346-5916346 + TCGA-AA-3502-01 COSM1348367 c.520C>T p.R174W Substitution - Missense 10:5906246-5906246 + SWE-4C COSM1179583 c.2260C>T p.R754W Substitution - Missense 10:5921264-5921264 + ML_06_T_01 COSM5037701 c.2079C>T p.D693D Substitution - coding silent 10:5917639-5917639 + BD72T COSM5512645 c.677C>A p.A226E Substitution - Missense 10:5906403-5906403 + TCGA-DK-A2I1-01 COSM1297332 c.2002G>C p.E668Q Substitution - Missense 10:5917480-5917480 + TCGA-A6-6780-01 COSM3686968 c.3016G>A p.V1006I Substitution - Missense 10:5936489-5936489 + T12 COSM4441591 c.1636G>A p.A546T Substitution - Missense 10:5915489-5915489 + TCGA-13-2065-01 COSM1321284 c.718C>G p.P240A Substitution - Missense 10:5906444-5906444 + ESO-717 COSM1242272 c.2623T>C p.Y875H Substitution - Missense 10:5924382-5924382 + S02065 COSM5672530 c.2374A>G p.K792E Substitution - Missense 10:5921468-5921468 + TCGA-61-1727-01 COSM1321283 c.2939T>G p.L980R Substitution - Missense 10:5927498-5927498 + TCGA-46-3765-01 COSM684839 c.2005G>A p.E669K Substitution - Missense 10:5917483-5917483 + TCGA-EE-A20C-06 COSM3439075 c.3189C>T p.F1063F Substitution - coding silent 10:5937184-5937184 + 587384 COSM1206805 c.1606T>C p.F536L Substitution - Missense 10:5915459-5915459 + BK0006 COSM4185597 c.729T>G p.I243M Substitution - Missense 10:5906455-5906455 + PM-4 COSM5619900 c.2641G>T p.D881Y Substitution - Missense 10:5924400-5924400 + CHC892T COSM4798038 c.1870A>G p.I624V Substitution - Missense 10:5916385-5916385 + TCGA-AA-3984-01 COSM297874 c.2551C>T p.Q851* Substitution - Nonsense 10:5923696-5923696 + I2L-P28-Tumor-Organoid COSM4533910 c.2029G>A p.G677S Substitution - Missense 10:5917507-5917507 + TCGA-G2-A2EF-01 COSM1297331 c.1405A>T p.N469Y Substitution - Missense 10:5913787-5913787 + I2L-P28-Tumor-Biopsy COSM4533910 c.2029G>A p.G677S Substitution - Missense 10:5917507-5917507 + ESCC_71 COSM5634101 c.147C>T p.H49H Substitution - coding silent 10:5895180-5895180 + CSCC-31-T COSM4468798 c.1563C>T p.T521T Substitution - coding silent 10:5915416-5915416 + TCGA-DS-A1OC-01 COSM1293288 c.2698G>T p.E900* Substitution - Nonsense 10:5924457-5924457 + TCGA-HU-A4GT-01 COSM4014831 c.1268G>A p.S423N Substitution - Missense 10:5911032-5911032 + H650 COSM1194273 c.1029C>A p.N343K Substitution - Missense 10:5909047-5909047 + 2497767 COSM3686968 c.3016G>A p.V1006I Substitution - Missense 10:5936489-5936489 + CCK81 COSM2148045 c.605A>G p.H202R Substitution - Missense 10:5906331-5906331 + TCGA-EI-6917-01 COSM3415123 c.2632G>A p.A878T Substitution - Missense 10:5924391-5924391 + TCGA-EE-A3AG-06 COSM3439076 c.3243C>T p.I1081I Substitution - coding silent 10:5937238-5937238 + pfg122T COSM4749253 c.2957T>C p.L986S Substitution - Missense 10:5927516-5927516 + TCGA-AP-A051-01 COSM919132 c.1701C>T p.Y567Y Substitution - coding silent 10:5915554-5915554 + CHC892T COSM4959682 c.2547G>A p.R849R Substitution - coding silent 10:5923692-5923692 + PD6404a COSM2148083 c.2412C>T p.N804N Substitution - coding silent 10:5921506-5921506 + CSCC-4-T COSM3439072 c.1780C>T p.L594F Substitution - Missense 10:5916295-5916295 + TCGA-AP-A059-01 COSM919127 c.592G>A p.A198T Substitution - Missense 10:5906318-5906318 + TCGA-G4-6309-01 COSM1348372 c.3048G>A p.V1016V Substitution - coding silent 10:5936521-5936521 + TCGA-E2-A1LG-01 COSM1474678 c.730C>G p.P244A Substitution - Missense 10:5906456-5906456 + Gp5D COSM2148094 c.3215G>A p.R1072H Substitution - Missense 10:5937210-5937210 + TCGA-AA-3663-01 COSM1348373 c.3074T>C p.V1025A Substitution - Missense 10:5936547-5936547 + TCGA-UB-A7ME-01 COSM4910115 c.288G>C p.P96P Substitution - coding silent 10:5903153-5903153 + SNU-175 COSM2148081 c.2261G>A p.R754Q Substitution - Missense 10:5921265-5921265 + TCGA-EE-A2GU-06 COSM3439068 c.491C>T p.S164L Substitution - Missense 10:5906217-5906217 + CHOL44 COSM1743338 c.3169C>T p.R1057C Substitution - Missense 10:5937164-5937164 + WA56 COSM239844 c.3014A>G p.N1005S Substitution - Missense 10:5936487-5936487 + T15 COSM5341271 c.237C>T p.F79F Substitution - coding silent 10:5903102-5903102 + LUAD-F00368 COSM340880 c.572G>T p.W191L Substitution - Missense 10:5906298-5906298 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.498543 10p15.1 607222

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.I836V c.2506A>G 10 5965614 COREAD A G Missense p.R211G c.631A>G 10 5948320 STAD A T Missense p.I629F c.1885A>T 10 5958363 OV A T Missense p.N469Y c.1405A>T 10 5955750 BLCA ATTTTGTGA - MultiAAMissense p.D939_K942delinsE c.2817_2825delTTTTGTGAA 10 5967396 RCCC C A Missense p.A1062E c.3185C>A 10 5979143 LUSC C A Missense p.F79L c.237C>A 10 5945065 BLCA C A Missense p.R1057S c.3169C>A 10 5979127 ESCA C A Synonymous p.I719I c.2157C>A 10 5960345 CM C A Synonymous p.L383L c.1149C>A 10 5951233 BRCA C A Synonymous p.T1030T c.3090C>A 10 5978526 STAD C G Missense p.L492V c.1474C>G 10 5956157 COREAD C G Missense p.P169A c.505C>G 10 5948194 CM C G Missense p.P244A c.730C>G 10 5948419 BRCA C T IntronicSNV . c.1718+99C>T 10 5957633 CM C T IntronicSNV . c.2552-49C>T 10 5966225 CM C T IntronicSNV . c.3114+125C>T 10 5978675 CM C T Missense p.A377V c.1130C>T 10 5951214 HNSC C T Missense p.L594F c.1780C>T 10 5958258 CM C T Missense p.P199S c.595C>T 10 5948284 HNSC C T Missense p.P279S c.835C>T 10 5948524 CM C T Missense p.P359L c.1076C>T 10 5951160 HNSC C T Missense p.P384L c.1151C>T 10 5951235 COREAD C T Missense p.P481L c.1442C>T 10 5955787 LUAD C T Missense p.P844S c.2530C>T 10 5965638 CM C T Missense p.R200W c.598C>T 10 5948287 UCEC C T Missense p.R551C c.1651C>T 10 5957467 STAD C T Missense p.S164L c.491C>T 10 5948180 CM C T Missense p.S482F c.1445C>T 10 5955790 LUAD C T Nonsense p.Q491* c.1471C>T 10 5956154 CM C T Nonsense p.Q508* c.1522C>T 10 5956205 HNSC C T Nonsense p.Q81* c.241C>T 10 5945069 BRCA C T Synonymous p.F1063F c.3189C>T 10 5979147 CM C T Synonymous p.F277F c.831C>T 10 5948520 THCA C T Synonymous p.F817F c.2451C>T 10 5963508 CM C T Synonymous p.I1081I c.3243C>T 10 5979201 CM C T Synonymous p.I111I c.333C>T 10 5948022 CM C T Synonymous p.L287L c.859C>T 10 5948548 CM C T Synonymous p.N802N c.2406C>T 10 5963463 ESCA C T Synonymous p.S150S c.450C>T 10 5948139 LUSC C T Synonymous p.S685S c.2055C>T 10 5959578 BRCA G A Missense p.C353Y c.1058G>A 10 5951142 RCCC G A Missense p.E374K c.1120G>A 10 5951204 BLCA G A Missense p.E669K c.2005G>A 10 5959446 LUSC G A Missense p.G239D c.716G>A 10 5948405 HNSC G A Missense p.R1057H c.3170G>A 10 5979128 LGG G A Missense p.R346Q c.1037G>A 10 5951018 BRCA G A Missense p.R346Q c.1037G>A 10 5951018 HNSC G A Missense p.R979H c.2936G>A 10 5969458 CM G A Missense p.V1016M c.3046G>A 10 5978482 COREAD G A Missense p.V1093I c.3277G>A 10 5979235 PRAD G A Missense p.V1093I c.3277G>A 10 5979235 SCLC G A Missense p.V746I c.2236G>A 10 5960424 UCEC G A Missense p.V773I c.2317G>A 10 5963284 RCCC G A Synonymous p.P279P c.837G>A 10 5948526 PRAD G A Synonymous p.V75V c.225G>A 10 5945053 BRCA G C IntronicSNV . c.2029+5G>C 10 5959475 BRCA G C Missense p.E668Q c.2002G>C 10 5959443 BLCA G C Missense p.E995Q c.2983G>C 10 5978419 OV G - Frameshift p.K598Rfs*5 c.1791delG 10 5958267 HNSC GGAGAA - InFrameDeletion p.E447_K448delEK c.1340_1345delAGAAGG 10 5953065 RCCC G T Missense p.A41S c.121G>T 10 5937117 BRCA G T Missense p.G27W c.79G>T 10 5937075 RCCC G T Missense p.M144I c.432G>T 10 5948121 LUAD G T Missense p.S685I c.2054G>T 10 5959577 BRCA G T Missense p.V280L c.838G>T 10 5948527 CM G T Missense p.V280L c.838G>T 10 5948527 LGG G T SpliceAcceptorSNV . c.1458-1G>T 10 5956140 LUAD G T SpliceAcceptorSNV . c.2254-1G>T 10 5963220 BRCA G T Synonymous p.T425T c.1275G>T 10 5953002 HNSC G T Synonymous p.V440V c.1320G>T 10 5953047 CM T A Missense p.Y729N c.2185T>A 10 5960373 CM T C Synonymous p.F615F c.1845T>C 10 5958323 HNSC T C Synonymous p.S159S c.477T>C 10 5948166 RCCC