Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 6 79650578 79650578 + Missense_Mutation SNP C C G TCGA-BT-A20N-01A-11D-A14W-08 TCGA-BT-A20N-11A-11D-A14W-08 g.chr6:79650578C>G c.5298G>C c.(5296-5298)atG>atC p.M1766I BLCA 6 79650642 79650642 + Missense_Mutation SNP T T A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr6:79650642T>A c.5234A>T c.(5233-5235)aAg>aTg p.K1745M BLCA 6 79655145 79655145 + Missense_Mutation SNP C C G TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr6:79655145C>G c.4700G>C c.(4699-4701)aGt>aCt p.S1567T BLCA 6 79655867 79655867 + Missense_Mutation SNP A A G TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr6:79655867A>G c.4481T>C c.(4480-4482)aTa>aCa p.I1494T BLCA 6 79711637 79711637 + Nonsense_Mutation SNP G G A TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr6:79711637G>A c.1858C>T c.(1858-1860)Cag>Tag p.Q620* BLCA 6 79711644 79711644 + Silent SNP G G A TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr6:79711644G>A c.1851C>T c.(1849-1851)ctC>ctT p.L617L BLCA 6 79711676 79711676 + Missense_Mutation SNP G G A TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr6:79711676G>A c.1819C>T c.(1819-1821)Cct>Tct p.P607S BLCA 6 79713497 79713497 + Missense_Mutation SNP G G A TCGA-BT-A42E-01A-11D-A23U-08 TCGA-BT-A42E-10A-01D-A23U-08 g.chr6:79713497G>A c.1603C>T c.(1603-1605)Cat>Tat p.H535Y BLCA 6 79724924 79724924 + Missense_Mutation SNP C C G TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr6:79724924C>G c.1399G>C c.(1399-1401)Gat>Cat p.D467H BLCA 6 79727268 79727268 + Missense_Mutation SNP G G A TCGA-C4-A0F1-01A-11D-A10S-08 TCGA-C4-A0F1-10A-01D-A10S-08 g.chr6:79727268G>A c.1027C>T c.(1027-1029)Cat>Tat p.H343Y BRCA 6 79655835 79655835 + Nonsense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:79655835G>A c.4513C>T c.(4513-4515)Cga>Tga p.R1505* BRCA 6 79664655 79664655 + Missense_Mutation SNP C C T TCGA-BH-A5IZ-01A-11D-A27P-09 TCGA-BH-A5IZ-11A-13D-A27P-09 g.chr6:79664655C>T c.3929G>A c.(3928-3930)cGt>cAt p.R1310H BRCA 6 79665349 79665351 + In_Frame_Del DEL TTC TTC - TCGA-E2-A1B1-01A-21D-A12Q-09 TCGA-E2-A1B1-10A-01D-A12Q-09 g.chr6:79665349_79665351delTTC c.3831_3833delGAA c.(3829-3834)aagaaa>aaa p.1277_1278KK>K BRCA 6 79672892 79672892 + Missense_Mutation SNP C C T TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr6:79672892C>T c.3457G>A c.(3457-3459)Gat>Aat p.D1153N BRCA 6 79675691 79675691 + Silent SNP A A G TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr6:79675691A>G c.3288T>C c.(3286-3288)ccT>ccC p.P1096P BRCA 6 79688311 79688311 + Missense_Mutation SNP C C T TCGA-C8-A12T-01A-11D-A10Y-09 TCGA-C8-A12T-10A-01D-A110-09 g.chr6:79688311C>T c.2887G>A c.(2887-2889)Gag>Aag p.E963K BRCA 6 79692714 79692716 + In_Frame_Del DEL TTC TTC - TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr6:79692714_79692716delTTC c.2656_2658delGAA c.(2656-2658)gaadel p.E886del BRCA 6 79698009 79698009 + Frame_Shift_Del DEL G G - TCGA-E2-A56Z-01A-12D-A29N-09 TCGA-E2-A56Z-10A-01D-A29N-09 g.chr6:79698009delG c.2377delC c.(2377-2379)caafs p.Q793fs BRCA 6 79698011 79698011 + Missense_Mutation SNP T T A TCGA-E2-A56Z-01A-12D-A29N-09 TCGA-E2-A56Z-10A-01D-A29N-09 g.chr6:79698011T>A c.2375A>T c.(2374-2376)aAt>aTt p.N792I BRCA 6 79698060 79698060 + Missense_Mutation SNP C C T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr6:79698060C>T c.2326G>A c.(2326-2328)Gct>Act p.A776T BRCA 6 79725353 79725353 + Silent SNP G G C TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr6:79725353G>C c.1383C>G c.(1381-1383)gtC>gtG p.V461V BRCA 6 79725444 79725444 + Missense_Mutation SNP G G T TCGA-E9-A1RF-01A-11D-A159-09 TCGA-E9-A1RF-10A-01D-A159-09 g.chr6:79725444G>T c.1292C>A c.(1291-1293)gCt>gAt p.A431D CESC 6 79650622 79650622 + Missense_Mutation SNP C C T TCGA-C5-A1M7-01A-11D-A13W-08 TCGA-C5-A1M7-10A-01D-A13W-08 g.chr6:79650622C>T c.5254G>A c.(5254-5256)Gag>Aag p.E1752K CESC 6 79655921 79655921 + Missense_Mutation SNP G G A TCGA-Q1-A6DT-01A-11D-A32I-09 TCGA-Q1-A6DT-10A-01D-A32I-09 g.chr6:79655921G>A c.4427C>T c.(4426-4428)tCt>tTt p.S1476F CHOL 6 79679836 79679836 + Missense_Mutation SNP G G C TCGA-4G-AAZT-01A-11D-A417-09 TCGA-4G-AAZT-10A-01D-A41A-09 g.chr6:79679836G>C c.3052C>G c.(3052-3054)Ctt>Gtt p.L1018V CHOL 6 79707219 79707219 + Missense_Mutation SNP C C T TCGA-W5-AA2H-01A-31D-A417-09 TCGA-W5-AA2H-10A-01D-A41A-09 g.chr6:79707219C>T c.2113G>A c.(2113-2115)Gca>Aca p.A705T COAD 6 79650559 79650559 + Nonsense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr6:79650559G>A c.5317C>T c.(5317-5319)Cga>Tga p.R1773* COAD 6 79650575 79650575 + Silent SNP T T C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr6:79650575T>C c.5301A>G c.(5299-5301)agA>agG p.R1767R COAD 6 79650575 79650575 + Silent SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr6:79650575T>C c.5301A>G c.(5299-5301)agA>agG p.R1767R COAD 6 79650745 79650745 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:79650745G>A c.5131C>T c.(5131-5133)Cgt>Tgt p.R1711C COAD 6 79650885 79650885 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:79650885T>G c.4991A>C c.(4990-4992)aAa>aCa p.K1664T COAD 6 79655055 79655055 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr6:79655055G>A c.4790C>T c.(4789-4791)gCg>gTg p.A1597V COAD 6 79655099 79655099 + Silent SNP T T C TCGA-D5-6534-01A-21D-1924-10 TCGA-D5-6534-10A-01D-1924-10 g.chr6:79655099T>C c.4746A>G c.(4744-4746)gaA>gaG p.E1582E COAD 6 79655100 79655100 + Missense_Mutation SNP T T C TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr6:79655100T>C c.4745A>G c.(4744-4746)gAa>gGa p.E1582G COAD 6 79655100 79655100 + Missense_Mutation SNP T T C TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr6:79655100T>C c.4745A>G c.(4744-4746)gAa>gGa p.E1582G COAD 6 79655939 79655939 + Missense_Mutation SNP T T A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr6:79655939T>A c.4409A>T c.(4408-4410)aAa>aTa p.K1470I COAD 6 79656492 79656492 + Missense_Mutation SNP T T C TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr6:79656492T>C c.4306A>G c.(4306-4308)Acc>Gcc p.T1436A COAD 6 79656520 79656520 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr6:79656520T>G c.4278A>C c.(4276-4278)aaA>aaC p.K1426N COAD 6 79657426 79657426 + Missense_Mutation SNP T T C TCGA-AA-3861-01A-01W-0995-10 TCGA-AA-3861-10A-01W-0995-10 g.chr6:79657426T>C c.4120A>G c.(4120-4122)Aat>Gat p.N1374D COAD 6 79664552 79664552 + Silent SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr6:79664552C>T c.4032G>A c.(4030-4032)ccG>ccA p.P1344P COAD 6 79664552 79664552 + Silent SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr6:79664552C>T c.4032G>A c.(4030-4032)ccG>ccA p.P1344P COAD 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L COAD 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L COAD 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L COAD 6 79664655 79664655 + Missense_Mutation SNP C C T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr6:79664655C>T c.3929G>A c.(3928-3930)cGt>cAt p.R1310H COAD 6 79665344 79665344 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:79665344A>C c.3838T>G c.(3838-3840)Ttg>Gtg p.L1280V COAD 6 79665401 79665401 + Splice_Site SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:79665401T>C c.e33-2 COAD 6 79668299 79668299 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr6:79668299C>T c.3675G>A c.(3673-3675)atG>atA p.M1225I COAD 6 79675691 79675691 + Silent SNP A A G TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr6:79675691A>G c.3288T>C c.(3286-3288)ccT>ccC p.P1096P COAD 6 79679609 79679609 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr6:79679609C>T c.3148G>A c.(3148-3150)Gat>Aat p.D1050N COAD 6 79680570 79680570 + Silent SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr6:79680570G>A c.2925C>T c.(2923-2925)gtC>gtT p.V975V COAD 6 79680570 79680570 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:79680570G>A c.2925C>T c.(2923-2925)gtC>gtT p.V975V COAD 6 79692617 79692617 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:79692617C>A c.2755G>T c.(2755-2757)Gaa>Taa p.E919* COAD 6 79692630 79692630 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:79692630T>G c.2742A>C c.(2740-2742)aaA>aaC p.K914N COAD 6 79697996 79697996 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:79697996C>T c.2390G>A c.(2389-2391)cGt>cAt p.R797H COAD 6 79698055 79698055 + Silent SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr6:79698055A>G c.2331T>C c.(2329-2331)caT>caC p.H777H COAD 6 79707161 79707161 + Missense_Mutation SNP A A G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr6:79707161A>G c.2171T>C c.(2170-2172)gTa>gCa p.V724A COAD 6 79707219 79707219 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr6:79707219C>T c.2113G>A c.(2113-2115)Gca>Aca p.A705T COAD 6 79707219 79707219 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr6:79707219C>T c.2113G>A c.(2113-2115)Gca>Aca p.A705T COAD 6 79707227 79707227 + Missense_Mutation SNP T T A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr6:79707227T>A c.2105A>T c.(2104-2106)cAc>cTc p.H702L COAD 6 79724918 79724918 + Missense_Mutation SNP C C T TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr6:79724918C>T c.1405G>A c.(1405-1407)Gta>Ata p.V469I COAD 6 79725475 79725475 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:79725475T>G c.1261A>C c.(1261-1263)Aaa>Caa p.K421Q COAD 6 79727098 79727098 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:79727098T>G c.1101A>C c.(1099-1101)aaA>aaC p.K367N COAD 6 79727259 79727259 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:79727259G>A c.1036C>T c.(1036-1038)Cgg>Tgg p.R346W COAD 6 79735718 79735718 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr6:79735718C>T c.764G>A c.(763-765)cGa>cAa p.R255Q COAD 6 79735744 79735744 + Silent SNP A A G TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr6:79735744A>G c.738T>C c.(736-738)gaT>gaC p.D246D COAD 6 79735745 79735745 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr6:79735745T>C c.737A>G c.(736-738)gAt>gGt p.D246G COAD 6 79752673 79752673 + Nonsense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr6:79752673G>A c.487C>T c.(487-489)Cga>Tga p.R163* COAD 6 79770286 79770286 + Missense_Mutation SNP C C G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:79770286C>G c.348G>C c.(346-348)aaG>aaC p.K116N COAD 6 79770396 79770396 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr6:79770396C>T c.329G>A c.(328-330)cGc>cAc p.R110H COAD 6 79770437 79770437 + Silent SNP T T C TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr6:79770437T>C c.288A>G c.(286-288)ggA>ggG p.G96G COADREAD 6 79650559 79650559 + Nonsense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr6:79650559G>A c.5317C>T c.(5317-5319)Cga>Tga p.R1773* COADREAD 6 79650575 79650575 + Silent SNP T T C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr6:79650575T>C c.5301A>G c.(5299-5301)agA>agG p.R1767R COADREAD 6 79650575 79650575 + Silent SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr6:79650575T>C c.5301A>G c.(5299-5301)agA>agG p.R1767R COADREAD 6 79650577 79650577 + Missense_Mutation SNP T T C TCGA-DC-6155-01A-11D-1657-10 TCGA-DC-6155-10A-01D-1657-10 g.chr6:79650577T>C c.5299A>G c.(5299-5301)Aga>Gga p.R1767G COADREAD 6 79650745 79650745 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:79650745G>A c.5131C>T c.(5131-5133)Cgt>Tgt p.R1711C COADREAD 6 79650763 79650763 + Missense_Mutation SNP A A C TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr6:79650763A>C c.5113T>G c.(5113-5115)Ttg>Gtg p.L1705V COADREAD 6 79650885 79650885 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:79650885T>G c.4991A>C c.(4990-4992)aAa>aCa p.K1664T COADREAD 6 79655055 79655055 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr6:79655055G>A c.4790C>T c.(4789-4791)gCg>gTg p.A1597V COADREAD 6 79655099 79655099 + Silent SNP T T C TCGA-D5-6534-01A-21D-1924-10 TCGA-D5-6534-10A-01D-1924-10 g.chr6:79655099T>C c.4746A>G c.(4744-4746)gaA>gaG p.E1582E COADREAD 6 79655100 79655100 + Missense_Mutation SNP T T C TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr6:79655100T>C c.4745A>G c.(4744-4746)gAa>gGa p.E1582G COADREAD 6 79655100 79655100 + Missense_Mutation SNP T T C TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr6:79655100T>C c.4745A>G c.(4744-4746)gAa>gGa p.E1582G COADREAD 6 79655100 79655100 + Missense_Mutation SNP T T C TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr6:79655100T>C c.4745A>G c.(4744-4746)gAa>gGa p.E1582G COADREAD 6 79655764 79655764 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:79655764C>A c.4584G>T c.(4582-4584)aaG>aaT p.K1528N COADREAD 6 79655939 79655939 + Missense_Mutation SNP T T A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr6:79655939T>A c.4409A>T c.(4408-4410)aAa>aTa p.K1470I COADREAD 6 79656492 79656492 + Missense_Mutation SNP T T C TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr6:79656492T>C c.4306A>G c.(4306-4308)Acc>Gcc p.T1436A COADREAD 6 79656520 79656520 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr6:79656520T>G c.4278A>C c.(4276-4278)aaA>aaC p.K1426N COADREAD 6 79657426 79657426 + Missense_Mutation SNP T T C TCGA-AA-3861-01A-01W-0995-10 TCGA-AA-3861-10A-01W-0995-10 g.chr6:79657426T>C c.4120A>G c.(4120-4122)Aat>Gat p.N1374D COADREAD 6 79657465 79657465 + Missense_Mutation SNP T T C TCGA-DC-6158-01A-11D-1657-10 TCGA-DC-6158-10A-01D-1657-10 g.chr6:79657465T>C c.4081A>G c.(4081-4083)Atg>Gtg p.M1361V COADREAD 6 79664552 79664552 + Silent SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr6:79664552C>T c.4032G>A c.(4030-4032)ccG>ccA p.P1344P COADREAD 6 79664552 79664552 + Silent SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr6:79664552C>T c.4032G>A c.(4030-4032)ccG>ccA p.P1344P COADREAD 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L COADREAD 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L COADREAD 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L COADREAD 6 79664655 79664655 + Missense_Mutation SNP C C T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr6:79664655C>T c.3929G>A c.(3928-3930)cGt>cAt p.R1310H COADREAD 6 79665344 79665344 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:79665344A>C c.3838T>G c.(3838-3840)Ttg>Gtg p.L1280V COADREAD 6 79665401 79665401 + Splice_Site SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:79665401T>C c.e33-2 COADREAD 6 79668299 79668299 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr6:79668299C>T c.3675G>A c.(3673-3675)atG>atA p.M1225I COADREAD 6 79675473 79675473 + Missense_Mutation SNP T T G TCGA-AG-4007-01A-01W-1073-09 TCGA-AG-4007-10A-01W-1073-09 g.chr6:79675473T>G c.3326A>C c.(3325-3327)aAt>aCt p.N1109T COADREAD 6 79675691 79675691 + Silent SNP A A G TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr6:79675691A>G c.3288T>C c.(3286-3288)ccT>ccC p.P1096P COADREAD 6 79679609 79679609 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr6:79679609C>T c.3148G>A c.(3148-3150)Gat>Aat p.D1050N COADREAD 6 79680570 79680570 + Silent SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr6:79680570G>A c.2925C>T c.(2923-2925)gtC>gtT p.V975V COADREAD 6 79680570 79680570 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:79680570G>A c.2925C>T c.(2923-2925)gtC>gtT p.V975V COADREAD 6 79680570 79680570 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:79680570G>A c.2925C>T c.(2923-2925)gtC>gtT p.V975V COADREAD 6 79692617 79692617 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:79692617C>A c.2755G>T c.(2755-2757)Gaa>Taa p.E919* COADREAD 6 79692630 79692630 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:79692630T>G c.2742A>C c.(2740-2742)aaA>aaC p.K914N COADREAD 6 79692787 79692787 + Missense_Mutation SNP T T C TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr6:79692787T>C c.2585A>G c.(2584-2586)aAt>aGt p.N862S COADREAD 6 79697996 79697996 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:79697996C>T c.2390G>A c.(2389-2391)cGt>cAt p.R797H COADREAD 6 79698055 79698055 + Silent SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr6:79698055A>G c.2331T>C c.(2329-2331)caT>caC p.H777H COADREAD 6 79707161 79707161 + Missense_Mutation SNP A A G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr6:79707161A>G c.2171T>C c.(2170-2172)gTa>gCa p.V724A COADREAD 6 79707219 79707219 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr6:79707219C>T c.2113G>A c.(2113-2115)Gca>Aca p.A705T COADREAD 6 79707219 79707219 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr6:79707219C>T c.2113G>A c.(2113-2115)Gca>Aca p.A705T COADREAD 6 79707220 79707220 + Silent SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr6:79707220G>A c.2112C>T c.(2110-2112)aaC>aaT p.N704N COADREAD 6 79707227 79707227 + Missense_Mutation SNP T T A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr6:79707227T>A c.2105A>T c.(2104-2106)cAc>cTc p.H702L COADREAD 6 79724918 79724918 + Missense_Mutation SNP C C T TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr6:79724918C>T c.1405G>A c.(1405-1407)Gta>Ata p.V469I COADREAD 6 79725475 79725475 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:79725475T>G c.1261A>C c.(1261-1263)Aaa>Caa p.K421Q COADREAD 6 79726343 79726343 + Missense_Mutation SNP G G A TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr6:79726343G>A c.1153C>T c.(1153-1155)Cgt>Tgt p.R385C COADREAD 6 79727098 79727098 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:79727098T>G c.1101A>C c.(1099-1101)aaA>aaC p.K367N COADREAD 6 79727259 79727259 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:79727259G>A c.1036C>T c.(1036-1038)Cgg>Tgg p.R346W COADREAD 6 79728820 79728820 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:79728820G>T c.980C>A c.(979-981)tCt>tAt p.S327Y COADREAD 6 79735718 79735718 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr6:79735718C>T c.764G>A c.(763-765)cGa>cAa p.R255Q COADREAD 6 79735744 79735744 + Silent SNP A A G TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr6:79735744A>G c.738T>C c.(736-738)gaT>gaC p.D246D COADREAD 6 79735745 79735745 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr6:79735745T>C c.737A>G c.(736-738)gAt>gGt p.D246G COADREAD 6 79752673 79752673 + Nonsense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr6:79752673G>A c.487C>T c.(487-489)Cga>Tga p.R163* COADREAD 6 79770286 79770286 + Missense_Mutation SNP C C G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:79770286C>G c.348G>C c.(346-348)aaG>aaC p.K116N COADREAD 6 79770396 79770396 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr6:79770396C>T c.329G>A c.(328-330)cGc>cAc p.R110H COADREAD 6 79770437 79770437 + Silent SNP T T C TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr6:79770437T>C c.288A>G c.(286-288)ggA>ggG p.G96G DLBC 6 79671508 79671508 + Silent SNP C C T TCGA-FA-A6HN-01A-11D-A31X-10 TCGA-FA-A6HN-10A-01D-A31X-10 g.chr6:79671508C>T c.3555G>A c.(3553-3555)gtG>gtA p.V1185V DLBC 6 79700648 79700648 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr6:79700648C>T c.2256G>A c.(2254-2256)agG>agA p.R752R ESCA 6 79655198 79655198 + Silent SNP C C T TCGA-LN-A49L-01A-11D-A247-09 TCGA-LN-A49L-10A-01D-A247-09 g.chr6:79655198C>T c.4647G>A c.(4645-4647)gtG>gtA p.V1549V ESCA 6 79655907 79655907 + Missense_Mutation SNP G G T TCGA-IG-A97I-01A-11D-A387-09 TCGA-IG-A97I-10A-01D-A38A-09 g.chr6:79655907G>T c.4441C>A c.(4441-4443)Cct>Act p.P1481T ESCA 6 79668285 79668285 + Missense_Mutation SNP T T C TCGA-Q9-A6FU-01A-11D-A31U-09 TCGA-Q9-A6FU-10A-01D-A31U-09 g.chr6:79668285T>C c.3689A>G c.(3688-3690)tAt>tGt p.Y1230C ESCA 6 79692782 79692783 + Nonsense_Mutation DNP GC GC AA TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr6:79692782_79692783GC>AA c.2589_2590GC>TT c.(2587-2592)ctGCag>ctTTag p.Q864* ESCA 6 79698018 79698018 + Missense_Mutation SNP G G T TCGA-LN-A49R-01A-11D-A247-09 TCGA-LN-A49R-10A-01D-A247-09 g.chr6:79698018G>T c.2368C>A c.(2368-2370)Cag>Aag p.Q790K GBMLGG 6 79650981 79650981 + Nonsense_Mutation SNP G G C TCGA-CS-5390-01A-02D-1468-08 TCGA-CS-5390-10A-01D-1468-08 g.chr6:79650981G>C c.4895C>G c.(4894-4896)tCa>tGa p.S1632* GBMLGG 6 79650991 79650991 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79650991C>A c.4885G>T c.(4885-4887)Gga>Tga p.G1629* GBMLGG 6 79655810 79655810 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79655810A>G c.4538T>C c.(4537-4539)gTa>gCa p.V1513A GBMLGG 6 79657341 79657341 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79657341C>A c.4205G>T c.(4204-4206)aGg>aTg p.R1402M GBMLGG 6 79688363 79688363 + Missense_Mutation SNP C C G TCGA-DU-A5TU-01A-11D-A289-08 TCGA-DU-A5TU-10A-01D-A289-08 g.chr6:79688363C>G c.2835G>C c.(2833-2835)tgG>tgC p.W945C GBMLGG 6 79700587 79700587 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79700587T>C c.2317A>G c.(2317-2319)Aag>Gag p.K773E GBMLGG 6 79770432 79770432 + Missense_Mutation SNP T T G TCGA-P5-A737-01A-11D-A32B-08 TCGA-P5-A737-10A-01D-A329-08 g.chr6:79770432T>G c.293A>C c.(292-294)cAa>cCa p.Q98P HNSC 6 79650558 79650558 + Missense_Mutation SNP C C T TCGA-BB-A5HU-01A-11D-A28R-08 TCGA-BB-A5HU-10A-01D-A28U-08 g.chr6:79650558C>T c.5318G>A c.(5317-5319)cGa>cAa p.R1773Q HNSC 6 79655040 79655040 + Missense_Mutation SNP T T G TCGA-QK-A6IH-01A-11D-A31L-08 TCGA-QK-A6IH-10A-01D-A31J-08 g.chr6:79655040T>G c.4805A>C c.(4804-4806)aAg>aCg p.K1602T HNSC 6 79655791 79655791 + Missense_Mutation SNP C C A TCGA-F7-8489-01A-31D-2394-08 TCGA-F7-8489-10A-01D-2394-08 g.chr6:79655791C>A c.4557G>T c.(4555-4557)gaG>gaT p.E1519D HNSC 6 79655871 79655871 + Missense_Mutation SNP G G C TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr6:79655871G>C c.4477C>G c.(4477-4479)Cag>Gag p.Q1493E HNSC 6 79656513 79656513 + Missense_Mutation SNP G G C TCGA-BB-A5HU-01A-11D-A28R-08 TCGA-BB-A5HU-10A-01D-A28U-08 g.chr6:79656513G>C c.4285C>G c.(4285-4287)Ctt>Gtt p.L1429V HNSC 6 79657436 79657437 + Frame_Shift_Ins INS - - A TCGA-CQ-A4CE-01A-11D-A25Y-08 TCGA-CQ-A4CE-10A-01D-A25Y-08 g.chr6:79657436_79657437insA c.4109_4110insT c.(4108-4110)ttafs p.L1370fs HNSC 6 79665371 79665371 + Missense_Mutation SNP G G A TCGA-CV-7433-01A-11D-2129-08 TCGA-CV-7433-10A-01D-2129-08 g.chr6:79665371G>A c.3811C>T c.(3811-3813)Ctt>Ttt p.L1271F HNSC 6 79668289 79668289 + Nonsense_Mutation SNP G G A TCGA-CR-7395-01A-11D-2012-08 TCGA-CR-7395-10A-01D-2013-08 g.chr6:79668289G>A c.3685C>T c.(3685-3687)Cga>Tga p.R1229* HNSC 6 79679576 79679576 + Missense_Mutation SNP C C A TCGA-BA-4078-01A-01D-1434-08 TCGA-BA-4078-10A-01D-1434-08 g.chr6:79679576C>A c.3181G>T c.(3181-3183)Gca>Tca p.A1061S HNSC 6 79697996 79697996 + Missense_Mutation SNP C C T TCGA-CV-5443-01A-01D-1512-08 TCGA-CV-5443-11A-01D-1512-08 g.chr6:79697996C>T c.2390G>A c.(2389-2391)cGt>cAt p.R797H HNSC 6 79708024 79708024 + Missense_Mutation SNP T T C TCGA-IQ-A61G-01A-11D-A30E-08 TCGA-IQ-A61G-10A-01D-A30H-08 g.chr6:79708024T>C c.1964A>G c.(1963-1965)gAc>gGc p.D655G HNSC 6 79708071 79708071 + Missense_Mutation SNP C C G TCGA-UF-A71B-01A-12D-A34J-08 TCGA-UF-A71B-10B-01D-A34M-08 g.chr6:79708071C>G c.1917G>C c.(1915-1917)gaG>gaC p.E639D HNSC 6 79711634 79711634 + Missense_Mutation SNP T T A TCGA-CV-5432-01A-02D-1683-08 TCGA-CV-5432-10A-01D-1870-08 g.chr6:79711634T>A c.1861A>T c.(1861-1863)Atg>Ttg p.M621L HNSC 6 79770397 79770397 + Missense_Mutation SNP G G T TCGA-CV-5441-01A-01D-1512-08 TCGA-CV-5441-11A-01D-1512-08 g.chr6:79770397G>T c.328C>A c.(328-330)Cgc>Agc p.R110S HNSC 6 79787178 79787178 + Missense_Mutation SNP G G A TCGA-BB-4223-01A-01D-1434-08 TCGA-BB-4223-10A-01D-1434-08 g.chr6:79787178G>A c.176C>T c.(175-177)aCc>aTc p.T59I KICH 6 79711796 79711796 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr6:79711796G>A c.1699C>T c.(1699-1701)Cgt>Tgt p.R567C KIPAN 6 79650693 79650693 + Missense_Mutation SNP T T G TCGA-CJ-4905-01A-02D-1429-08 TCGA-CJ-4905-11A-01D-1429-08 g.chr6:79650693T>G c.5183A>C c.(5182-5184)gAt>gCt p.D1728A KIPAN 6 79655729 79655729 + Missense_Mutation SNP G G C TCGA-5P-A9JV-01A-12D-A42J-10 TCGA-5P-A9JV-10A-01D-A42M-10 g.chr6:79655729G>C c.4619C>G c.(4618-4620)cCa>cGa p.P1540R KIPAN 6 79655791 79655791 + Silent SNP C C T TCGA-PJ-A8JU-01A-11D-A35Z-10 TCGA-PJ-A8JU-10A-01D-A35Z-10 g.chr6:79655791C>T c.4557G>A c.(4555-4557)gaG>gaA p.E1519E KIPAN 6 79672856 79672856 + Missense_Mutation SNP A A G TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr6:79672856A>G c.3493T>C c.(3493-3495)Tgt>Cgt p.C1165R KIPAN 6 79708068 79708068 + Silent SNP G G A TCGA-BP-5196-01A-01D-1429-08 TCGA-BP-5196-11A-01D-1429-08 g.chr6:79708068G>A c.1920C>T c.(1918-1920)atC>atT p.I640I KIPAN 6 79711796 79711796 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr6:79711796G>A c.1699C>T c.(1699-1701)Cgt>Tgt p.R567C KIPAN 6 79724879 79724879 + Missense_Mutation SNP G G A TCGA-A4-8098-01A-11D-2396-08 TCGA-A4-8098-10A-01D-2396-08 g.chr6:79724879G>A c.1444C>T c.(1444-1446)Ctc>Ttc p.L482F KIRC 6 79650693 79650693 + Missense_Mutation SNP T T G TCGA-CJ-4905-01A-02D-1429-08 TCGA-CJ-4905-11A-01D-1429-08 g.chr6:79650693T>G c.5183A>C c.(5182-5184)gAt>gCt p.D1728A KIRC 6 79708068 79708068 + Silent SNP G G A TCGA-BP-5196-01A-01D-1429-08 TCGA-BP-5196-11A-01D-1429-08 g.chr6:79708068G>A c.1920C>T c.(1918-1920)atC>atT p.I640I KIRP 6 79655729 79655729 + Missense_Mutation SNP G G C TCGA-5P-A9JV-01A-12D-A42J-10 TCGA-5P-A9JV-10A-01D-A42M-10 g.chr6:79655729G>C c.4619C>G c.(4618-4620)cCa>cGa p.P1540R KIRP 6 79655791 79655791 + Silent SNP C C T TCGA-PJ-A8JU-01A-11D-A35Z-10 TCGA-PJ-A8JU-10A-01D-A35Z-10 g.chr6:79655791C>T c.4557G>A c.(4555-4557)gaG>gaA p.E1519E KIRP 6 79672856 79672856 + Missense_Mutation SNP A A G TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr6:79672856A>G c.3493T>C c.(3493-3495)Tgt>Cgt p.C1165R KIRP 6 79724879 79724879 + Missense_Mutation SNP G G A TCGA-A4-8098-01A-11D-2396-08 TCGA-A4-8098-10A-01D-2396-08 g.chr6:79724879G>A c.1444C>T c.(1444-1446)Ctc>Ttc p.L482F LAML 6 79664636 79664637 + Frame_Shift_Ins INS - - T TCGA-AB-2967-03A-01D-0739-09 TCGA-AB-2967-11A-01D-0739-09 g.chr6:79664636_79664637insT c.3947_3948insA c.(3946-3948)tacfs p.Y1316fs LAML 6 79735852 79735852 + Missense_Mutation SNP C C A TCGA-AB-2897-03A-01W-0733-08 TCGA-AB-2897-11A-01W-0732-08 g.chr6:79735852C>A c.630G>T c.(628-630)tgG>tgT p.W210C LGG 6 79650981 79650981 + Nonsense_Mutation SNP G G C TCGA-CS-5390-01A-02D-1468-08 TCGA-CS-5390-10A-01D-1468-08 g.chr6:79650981G>C c.4895C>G c.(4894-4896)tCa>tGa p.S1632* LGG 6 79650991 79650991 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79650991C>A c.4885G>T c.(4885-4887)Gga>Tga p.G1629* LGG 6 79655810 79655810 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79655810A>G c.4538T>C c.(4537-4539)gTa>gCa p.V1513A LGG 6 79657341 79657341 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79657341C>A c.4205G>T c.(4204-4206)aGg>aTg p.R1402M LGG 6 79688363 79688363 + Missense_Mutation SNP C C G TCGA-DU-A5TU-01A-11D-A289-08 TCGA-DU-A5TU-10A-01D-A289-08 g.chr6:79688363C>G c.2835G>C c.(2833-2835)tgG>tgC p.W945C LGG 6 79700587 79700587 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:79700587T>C c.2317A>G c.(2317-2319)Aag>Gag p.K773E LGG 6 79770432 79770432 + Missense_Mutation SNP T T G TCGA-P5-A737-01A-11D-A32B-08 TCGA-P5-A737-10A-01D-A329-08 g.chr6:79770432T>G c.293A>C c.(292-294)cAa>cCa p.Q98P LIHC 6 79679818 79679818 + Missense_Mutation SNP C C G TCGA-DD-AADS-01A-11D-A40R-10 TCGA-DD-AADS-10A-01D-A40U-10 g.chr6:79679818C>G c.3070G>C c.(3070-3072)Gct>Cct p.A1024P LIHC 6 79679863 79679863 + Missense_Mutation SNP T T C TCGA-DD-AACK-01A-11D-A40R-10 TCGA-DD-AACK-10A-01D-A40U-10 g.chr6:79679863T>C c.3025A>G c.(3025-3027)Ata>Gta p.I1009V LIHC 6 79688417 79688417 + Silent SNP C C G TCGA-LG-A6GG-01A-11D-A30V-10 TCGA-LG-A6GG-10A-01D-A30V-10 g.chr6:79688417C>G c.2781G>C c.(2779-2781)gtG>gtC p.V927V LIHC 6 79688429 79688429 + Splice_Site SNP C C A TCGA-DD-A1EB-01A-11D-A12Z-10 TCGA-DD-A1EB-10A-01D-A12Z-10 g.chr6:79688429C>A c.e24-1 LIHC 6 79692616 79692616 + Missense_Mutation SNP T T A TCGA-WJ-A86L-01A-12D-A45V-10 TCGA-WJ-A86L-10A-01D-A38X-10 g.chr6:79692616T>A c.2756A>T c.(2755-2757)gAa>gTa p.E919V LIHC 6 79692705 79692705 + Silent SNP T T C TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr6:79692705T>C c.2667A>G c.(2665-2667)aaA>aaG p.K889K LIHC 6 79727210 79727210 + Missense_Mutation SNP T T A TCGA-WJ-A86L-01A-12D-A45V-10 TCGA-WJ-A86L-10A-01D-A38X-10 g.chr6:79727210T>A c.1085A>T c.(1084-1086)gAg>gTg p.E362V LIHC 6 79727292 79727292 + Missense_Mutation SNP A A G TCGA-2Y-A9GV-01A-11D-A382-10 TCGA-2Y-A9GV-10A-01D-A385-10 g.chr6:79727292A>G c.1003T>C c.(1003-1005)Ttt>Ctt p.F335L LIHC 6 79752610 79752610 + Missense_Mutation SNP A A T TCGA-DD-A4NO-01A-11D-A28X-10 TCGA-DD-A4NO-10A-01D-A28X-10 g.chr6:79752610A>T c.550T>A c.(550-552)Tca>Aca p.S184T LIHC 6 79770201 79770201 + Missense_Mutation SNP T T A TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr6:79770201T>A c.433A>T c.(433-435)Agc>Tgc p.S145C LUAD 6 79650459 79650459 + Missense_Mutation SNP C C A TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr6:79650459C>A c.5417G>T c.(5416-5418)cGa>cTa p.R1806L LUAD 6 79650952 79650952 + Nonsense_Mutation SNP T T A TCGA-MP-A4SV-01A-11D-A24P-08 TCGA-MP-A4SV-10A-01D-A24P-08 g.chr6:79650952T>A c.4924A>T c.(4924-4926)Aaa>Taa p.K1642* LUAD 6 79655879 79655879 + Missense_Mutation SNP T T C TCGA-55-6971-01A-11D-1945-08 TCGA-55-6971-11A-01D-1945-08 g.chr6:79655879T>C c.4469A>G c.(4468-4470)aAt>aGt p.N1490S LUAD 6 79655973 79655973 + Missense_Mutation SNP C C T TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr6:79655973C>T c.4375G>A c.(4375-4377)Gaa>Aaa p.E1459K LUAD 6 79671407 79671407 + Splice_Site SNP C C A TCGA-MP-A4T7-01A-11D-A24P-08 TCGA-MP-A4T7-10A-01D-A24P-08 g.chr6:79671407C>A c.3656G>T c.(3655-3657)aGg>aTg p.R1219M LUAD 6 79695070 79695070 + Splice_Site SNP T T A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr6:79695070T>A c.2536A>T c.(2536-2538)Agt>Tgt p.S846C LUAD 6 79697925 79697925 + Splice_Site SNP C C T TCGA-05-4415-01A-22D-1855-08 TCGA-05-4415-10A-01D-1855-08 g.chr6:79697925C>T c.e21+1 LUAD 6 79726270 79726270 + Missense_Mutation SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr6:79726270C>A c.1226G>T c.(1225-1227)cGt>cTt p.R409L LUAD 6 79726319 79726319 + Nonsense_Mutation SNP G G A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr6:79726319G>A c.1177C>T c.(1177-1179)Caa>Taa p.Q393* LUAD 6 79735767 79735767 + Missense_Mutation SNP T T C TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr6:79735767T>C c.715A>G c.(715-717)Atg>Gtg p.M239V LUAD 6 79770483 79770483 + Missense_Mutation SNP C C A TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr6:79770483C>A c.242G>T c.(241-243)cGa>cTa p.R81L LUSC 6 79650528 79650528 + Missense_Mutation SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr6:79650528G>T c.5348C>A c.(5347-5349)tCt>tAt p.S1783Y LUSC 6 79650830 79650830 + Missense_Mutation SNP G G C TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr6:79650830G>C c.5046C>G c.(5044-5046)atC>atG p.I1682M LUSC 6 79650830 79650830 + Missense_Mutation SNP G G C TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr6:79650830G>C c.5046C>G c.(5044-5046)atC>atG p.I1682M LUSC 6 79655828 79655828 + Missense_Mutation SNP C C T TCGA-39-5022-01A-21D-1817-08 TCGA-39-5022-11A-01D-1817-08 g.chr6:79655828C>T c.4520G>A c.(4519-4521)aGa>aAa p.R1507K LUSC 6 79672829 79672829 + Missense_Mutation SNP G G T TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr6:79672829G>T c.3520C>A c.(3520-3522)Cag>Aag p.Q1174K LUSC 6 79672925 79672925 + Missense_Mutation SNP C C A TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr6:79672925C>A c.3424G>T c.(3424-3426)Ggt>Tgt p.G1142C LUSC 6 79688325 79688325 + Missense_Mutation SNP G G T TCGA-66-2744-01A-01D-0983-08 TCGA-66-2744-11A-01D-0983-08 g.chr6:79688325G>T c.2873C>A c.(2872-2874)cCa>cAa p.P958Q LUSC 6 79707136 79707136 + Silent SNP T T A TCGA-60-2723-01A-01D-1522-08 TCGA-60-2723-11A-01D-1522-08 g.chr6:79707136T>A c.2196A>T c.(2194-2196)gtA>gtT p.V732V LUSC 6 79725400 79725400 + Missense_Mutation SNP T T C TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr6:79725400T>C c.1336A>G c.(1336-1338)Atg>Gtg p.M446V LUSC 6 79752705 79752705 + Missense_Mutation SNP G G A TCGA-46-6026-01A-11D-1817-08 TCGA-46-6026-10A-01D-1817-08 g.chr6:79752705G>A c.455C>T c.(454-456)tCa>tTa p.S152L OV 6 79650905 79650905 + Silent SNP C C T TCGA-61-1725-01A-01W-0639-09 TCGA-61-1725-11A-01W-0639-09 g.chr6:79650905C>T c.4971G>A c.(4969-4971)aaG>aaA p.K1657K OV 6 79655099 79655099 + Silent SNP T T C TCGA-24-1544-01A-01W-0615-10 TCGA-24-1544-10A-01W-0615-10 g.chr6:79655099T>C c.4746A>G c.(4744-4746)gaA>gaG p.E1582E OV 6 79665394 79665394 + Missense_Mutation SNP T T A TCGA-61-1910-01A-01W-0639-09 TCGA-61-1910-11A-01W-0640-09 g.chr6:79665394T>A c.3788A>T c.(3787-3789)cAg>cTg p.Q1263L OV 6 79700592 79700592 + Missense_Mutation SNP A A G TCGA-20-1685-01A-01W-0633-09 TCGA-20-1685-10A-01W-0633-09 g.chr6:79700592A>G c.2312T>C c.(2311-2313)gTc>gCc p.V771A PAAD 6 79650542 79650542 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:79650542A>G c.5334T>C c.(5332-5334)taT>taC p.Y1778Y PAAD 6 79655783 79655783 + Missense_Mutation SNP G G A TCGA-2J-AABE-01A-12D-A40W-08 TCGA-2J-AABE-10A-01D-A40W-08 g.chr6:79655783G>A c.4565C>T c.(4564-4566)tCt>tTt p.S1522F PAAD 6 79655961 79655961 + Frame_Shift_Del DEL T T - TCGA-3A-A9IH-01A-12D-A397-08 TCGA-3A-A9IH-10A-01D-A39A-08 g.chr6:79655961delT c.4387delA c.(4387-4389)aggfs p.R1463fs PAAD 6 79655961 79655961 + Frame_Shift_Del DEL T T - TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr6:79655961delT c.4387delA c.(4387-4389)aggfs p.R1463fs PAAD 6 79655961 79655961 + Frame_Shift_Del DEL T T - TCGA-IB-7885-01A-11D-2154-08 TCGA-IB-7885-10A-01D-2154-08 g.chr6:79655961delT c.4387delA c.(4387-4389)aggfs p.R1463fs PAAD 6 79655978 79655978 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:79655978C>A c.e38-1 PAAD 6 79657339 79657339 + Splice_Site DEL C C - TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:79657339delC c.e36+1 PAAD 6 79668316 79668316 + Splice_Site SNP G G A TCGA-FB-AAQ3-01A-11D-A40W-08 TCGA-FB-AAQ3-11A-11D-A40W-08 g.chr6:79668316G>A c.3658C>T c.(3658-3660)Cgg>Tgg p.R1220W PAAD 6 79671415 79671415 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:79671415C>T c.3648G>A c.(3646-3648)agG>agA p.R1216R PAAD 6 79692681 79692681 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:79692681C>T c.2691G>A c.(2689-2691)aaG>aaA p.K897K PAAD 6 79711802 79711802 + Missense_Mutation SNP G G A TCGA-YY-A8LH-01A-11D-A36O-08 TCGA-YY-A8LH-10A-01D-A367-08 g.chr6:79711802G>A c.1693C>T c.(1693-1695)Ctt>Ttt p.L565F PAAD 6 79724895 79724895 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:79724895C>T c.1428G>A c.(1426-1428)ccG>ccA p.P476P PCPG 6 79675671 79675671 + Missense_Mutation SNP T T C TCGA-RW-A688-01A-11D-A35D-08 TCGA-RW-A688-10B-01D-A35B-08 g.chr6:79675671T>C c.3308A>G c.(3307-3309)tAc>tGc p.Y1103C PRAD 6 79672824 79672824 + Silent SNP C C T TCGA-KK-A8IC-01A-11D-A364-08 TCGA-KK-A8IC-11A-12D-A362-08 g.chr6:79672824C>T c.3525G>A c.(3523-3525)ttG>ttA p.L1175L PRAD 6 79692791 79692791 + Missense_Mutation SNP T T A TCGA-HC-A6AO-01A-11D-A30E-08 TCGA-HC-A6AO-10A-01D-A30H-08 g.chr6:79692791T>A c.2581A>T c.(2581-2583)Att>Ttt p.I861F PRAD 6 79713461 79713461 + Missense_Mutation SNP T T C TCGA-KC-A4BV-01A-31D-A26M-08 TCGA-KC-A4BV-10A-01D-A26K-08 g.chr6:79713461T>C c.1639A>G c.(1639-1641)Agc>Ggc p.S547G PRAD 6 79770385 79770385 + Splice_Site SNP T T A TCGA-QU-A6IM-01A-11D-A31L-08 TCGA-QU-A6IM-10A-01D-A31J-08 g.chr6:79770385T>A c.340A>T c.(340-342)Agc>Tgc p.S114C READ 6 79650577 79650577 + Missense_Mutation SNP T T C TCGA-DC-6155-01A-11D-1657-10 TCGA-DC-6155-10A-01D-1657-10 g.chr6:79650577T>C c.5299A>G c.(5299-5301)Aga>Gga p.R1767G READ 6 79650763 79650763 + Missense_Mutation SNP A A C TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr6:79650763A>C c.5113T>G c.(5113-5115)Ttg>Gtg p.L1705V READ 6 79655100 79655100 + Missense_Mutation SNP T T C TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr6:79655100T>C c.4745A>G c.(4744-4746)gAa>gGa p.E1582G READ 6 79655764 79655764 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:79655764C>A c.4584G>T c.(4582-4584)aaG>aaT p.K1528N READ 6 79657465 79657465 + Missense_Mutation SNP T T C TCGA-DC-6158-01A-11D-1657-10 TCGA-DC-6158-10A-01D-1657-10 g.chr6:79657465T>C c.4081A>G c.(4081-4083)Atg>Gtg p.M1361V READ 6 79675473 79675473 + Missense_Mutation SNP T T G TCGA-AG-4007-01A-01W-1073-09 TCGA-AG-4007-10A-01W-1073-09 g.chr6:79675473T>G c.3326A>C c.(3325-3327)aAt>aCt p.N1109T READ 6 79680570 79680570 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:79680570G>A c.2925C>T c.(2923-2925)gtC>gtT p.V975V READ 6 79692787 79692787 + Missense_Mutation SNP T T C TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr6:79692787T>C c.2585A>G c.(2584-2586)aAt>aGt p.N862S READ 6 79707220 79707220 + Silent SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr6:79707220G>A c.2112C>T c.(2110-2112)aaC>aaT p.N704N READ 6 79726343 79726343 + Missense_Mutation SNP G G A TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr6:79726343G>A c.1153C>T c.(1153-1155)Cgt>Tgt p.R385C READ 6 79728820 79728820 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:79728820G>T c.980C>A c.(979-981)tCt>tAt p.S327Y SARC 6 79707142 79707142 + Silent SNP A A G TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr6:79707142A>G c.2190T>C c.(2188-2190)gcT>gcC p.A730A SARC 6 79752576 79752576 + Missense_Mutation SNP C C T TCGA-DX-A8BQ-01A-11D-A37C-09 TCGA-DX-A8BQ-10A-01D-A37F-09 g.chr6:79752576C>T c.584G>A c.(583-585)gGc>gAc p.G195D SKCM 6 79650681 79650681 + Missense_Mutation SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr6:79650681G>A c.5195C>T c.(5194-5196)cCt>cTt p.P1732L SKCM 6 79650682 79650682 + Missense_Mutation SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr6:79650682G>A c.5194C>T c.(5194-5196)Cct>Tct p.P1732S SKCM 6 79655836 79655836 + Frame_Shift_Del DEL A A - TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr6:79655836delA c.4512delT c.(4510-4512)gttfs p.V1504fs SKCM 6 79664553 79664553 + Missense_Mutation SNP G G A TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr6:79664553G>A c.4031C>T c.(4030-4032)cCg>cTg p.P1344L SKCM 6 79664602 79664602 + Silent SNP A A G TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr6:79664602A>G c.3982T>C c.(3982-3984)Ttg>Ctg p.L1328L SKCM 6 79668244 79668244 + Missense_Mutation SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr6:79668244G>A c.3730C>T c.(3730-3732)Cct>Tct p.P1244S SKCM 6 79668245 79668245 + Silent SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr6:79668245G>A c.3729C>T c.(3727-3729)agC>agT p.S1243S SKCM 6 79671440 79671440 + Missense_Mutation SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr6:79671440G>A c.3623C>T c.(3622-3624)aCa>aTa p.T1208I SKCM 6 79708059 79708060 + Frame_Shift_Ins INS - - A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr6:79708059_79708060insA c.1928_1929insT c.(1927-1929)ctgfs p.L643fs SKCM 6 79725486 79725486 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:79725486C>T c.1250G>A c.(1249-1251)gGa>gAa p.G417E SKCM 6 79787191 79787191 + Missense_Mutation SNP C C T TCGA-ER-A19M-06A-61D-A23B-08 TCGA-ER-A19M-10A-01D-A23B-08 g.chr6:79787191C>T c.163G>A c.(163-165)Gag>Aag p.E55K SKCM 6 79787588 79787588 + Missense_Mutation SNP C C T TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr6:79787588C>T c.83G>A c.(82-84)tGt>tAt p.C28Y

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 6 79713493 79713493 single base substitution C G missense_variant G536A 1607G>C BLCA-US 6 79650578 79650578 single base substitution C G exon_variant BLCA-US 6 79650578 79650578 single base substitution C G missense_variant M1766I 5298G>C BLCA-US 6 79655145 79655145 single base substitution C G exon_variant BLCA-US 6 79655145 79655145 single base substitution C G missense_variant S1567T 4700G>C BLCA-US 6 79727268 79727268 single base substitution G A missense_variant H343Y 1027C>T BOCA-FR 6 79668268 79668268 single base substitution G A exon_variant BOCA-FR 6 79668268 79668268 single base substitution G A stop_gained R1236* 3706C>T BOCA-FR 6 79697970 79697970 single base substitution G A missense_variant P806S 2416C>T BOCA-FR 6 79737516 79737516 single base substitution C T intron_variant BRCA-EU 6 79640635 79640635 single base substitution G C downstream_gene_variant BRCA-EU 6 79643049 79643049 single base substitution A G downstream_gene_variant BRCA-EU 6 79644864 79644864 single base substitution C A downstream_gene_variant BRCA-EU 6 79647022 79647022 single base substitution T C 3_prime_UTR_variant BRCA-EU 6 79647022 79647022 single base substitution T C downstream_gene_variant BRCA-EU 6 79647613 79647613 single base substitution A G 3_prime_UTR_variant BRCA-EU 6 79647613 79647613 single base substitution A G downstream_gene_variant BRCA-EU 6 79648157 79648157 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 6 79648157 79648157 deletion of <=200bp T - downstream_gene_variant BRCA-EU 6 79649555 79649555 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 6 79649555 79649555 insertion of <=200bp - A downstream_gene_variant BRCA-EU 6 79650037 79650037 single base substitution C G 3_prime_UTR_variant BRCA-EU 6 79650037 79650037 single base substitution C G downstream_gene_variant BRCA-EU 6 79657108 79657108 single base substitution C G intron_variant BRCA-EU 6 79658186 79658186 deletion of <=200bp T - intron_variant BRCA-EU 6 79658763 79658763 single base substitution C T intron_variant BRCA-EU 6 79659616 79659616 single base substitution G A intron_variant BRCA-EU 6 79659690 79659690 single base substitution G A intron_variant BRCA-EU 6 79659730 79659730 single base substitution T A intron_variant BRCA-EU 6 79659918 79659918 single base substitution A G intron_variant BRCA-EU 6 79661029 79661029 single base substitution G A intron_variant BRCA-EU 6 79661065 79661065 single base substitution G C intron_variant BRCA-EU 6 79662076 79662076 single base substitution T C intron_variant BRCA-EU 6 79662361 79662361 single base substitution T A intron_variant BRCA-EU 6 79664656 79664656 single base substitution G A exon_variant BRCA-EU 6 79664656 79664656 single base substitution G A missense_variant R1310C 3928C>T BRCA-EU 6 79665306 79665308 deletion of <=200bp TAA - intron_variant BRCA-EU 6 79666103 79666103 single base substitution C A exon_variant BRCA-EU 6 79666103 79666103 single base substitution C A intron_variant BRCA-EU 6 79666897 79666897 single base substitution G C exon_variant BRCA-EU 6 79666897 79666897 single base substitution G C intron_variant BRCA-EU 6 79667176 79667179 deletion of <=200bp ATTA - exon_variant BRCA-EU 6 79667176 79667179 deletion of <=200bp ATTA - intron_variant BRCA-EU 6 79667844 79667844 single base substitution G A exon_variant BRCA-EU 6 79667844 79667844 single base substitution G A intron_variant BRCA-EU 6 79670724 79670724 single base substitution G A intron_variant BRCA-EU 6 79670901 79670901 single base substitution C T intron_variant BRCA-EU 6 79672245 79672245 single base substitution C T intron_variant BRCA-EU 6 79673746 79673746 single base substitution A T intron_variant BRCA-EU 6 79673941 79673941 deletion of <=200bp A - intron_variant BRCA-EU 6 79673941 79673941 insertion of <=200bp - A intron_variant BRCA-EU 6 79675024 79675024 deletion of <=200bp A - intron_variant BRCA-EU 6 79675202 79675202 single base substitution A G intron_variant BRCA-EU 6 79675477 79675477 single base substitution C T exon_variant BRCA-EU 6 79675477 79675477 single base substitution C T missense_variant D1108N 3322G>A BRCA-EU 6 79675478 79675478 single base substitution C A exon_variant BRCA-EU 6 79675478 79675478 single base substitution C A missense_variant W1107C 3321G>T BRCA-EU 6 79676127 79676127 single base substitution C A intron_variant BRCA-EU 6 79678444 79678444 single base substitution C T intron_variant BRCA-EU 6 79678600 79678600 deletion of <=200bp T - intron_variant BRCA-EU 6 79678814 79678814 single base substitution G A intron_variant BRCA-EU 6 79678816 79678816 single base substitution G A intron_variant BRCA-EU 6 79679583 79679602 deletion of <=200bp AAATTGTTGTCTCAAGACTA - exon_variant BRCA-EU 6 79679583 79679602 deletion of <=200bp AAATTGTTGTCTCAAGACTA - frameshift_variant LVLRQQF1052 BRCA-EU 6 79680249 79680249 single base substitution T C intron_variant BRCA-EU 6 79680993 79680993 single base substitution T G intron_variant BRCA-EU 6 79681270 79681270 single base substitution G T intron_variant BRCA-EU 6 79681618 79681618 single base substitution C T intron_variant BRCA-EU 6 79682239 79682239 single base substitution G A intron_variant BRCA-EU 6 79682552 79682552 single base substitution A G intron_variant BRCA-EU 6 79684323 79684323 single base substitution C T intron_variant BRCA-EU 6 79685332 79685332 single base substitution C G intron_variant BRCA-EU 6 79687238 79687238 single base substitution A T intron_variant BRCA-EU 6 79688184 79688184 single base substitution A G intron_variant BRCA-EU 6 79688199 79688199 single base substitution G A intron_variant BRCA-EU 6 79688805 79688805 deletion of <=200bp T - intron_variant BRCA-EU 6 79690106 79690106 single base substitution G C intron_variant BRCA-EU 6 79691346 79691346 single base substitution A C intron_variant BRCA-EU 6 79691597 79691597 single base substitution A C intron_variant BRCA-EU 6 79692582 79692582 single base substitution T C intron_variant BRCA-EU 6 79695618 79695618 deletion of <=200bp T - intron_variant BRCA-EU 6 79695618 79695618 deletion of <=200bp T - upstream_gene_variant BRCA-EU 6 79696211 79696211 single base substitution G T intron_variant BRCA-EU 6 79696211 79696211 single base substitution G T upstream_gene_variant BRCA-EU 6 79697875 79697875 insertion of <=200bp - A intron_variant BRCA-EU 6 79698546 79698546 single base substitution G C intron_variant BRCA-EU 6 79700901 79700901 single base substitution G C intron_variant BRCA-EU 6 79701060 79701060 single base substitution G C intron_variant BRCA-EU 6 79702246 79702246 single base substitution A G intron_variant BRCA-EU 6 79702255 79702255 single base substitution T A intron_variant BRCA-EU 6 79703400 79703400 single base substitution G A intron_variant BRCA-EU 6 79709470 79709470 single base substitution A G intron_variant BRCA-EU 6 79709841 79709841 deletion of <=200bp T - intron_variant BRCA-EU 6 79711655 79711655 single base substitution C G missense_variant E614Q 1840G>C BRCA-EU 6 79713942 79713942 single base substitution G A intron_variant BRCA-EU 6 79715358 79715358 single base substitution T G intron_variant BRCA-EU 6 79715499 79715499 single base substitution A T intron_variant BRCA-EU 6 79717419 79717419 single base substitution C T intron_variant BRCA-EU 6 79718397 79718397 single base substitution G A intron_variant BRCA-EU 6 79720720 79720720 single base substitution G C intron_variant BRCA-EU 6 79724192 79724192 single base substitution T A intron_variant BRCA-EU 6 79724784 79724784 single base substitution G A intron_variant BRCA-EU 6 79725451 79725451 single base substitution T C missense_variant M429V 1285A>G BRCA-EU 6 79725883 79725883 single base substitution A G intron_variant BRCA-EU 6 79726053 79726053 deletion of <=200bp A - intron_variant BRCA-EU 6 79726658 79726658 single base substitution G A intron_variant BRCA-EU 6 79726928 79726928 single base substitution C G intron_variant BRCA-EU 6 79727943 79727943 single base substitution A G intron_variant BRCA-EU 6 79728257 79728257 deletion of <=200bp T - intron_variant BRCA-EU 6 79729278 79729278 single base substitution T G intron_variant BRCA-EU 6 79729322 79729322 single base substitution T G intron_variant BRCA-EU 6 79729761 79729761 single base substitution T C intron_variant BRCA-EU 6 79730270 79730270 deletion of <=200bp T - intron_variant BRCA-EU 6 79731656 79731656 single base substitution G C intron_variant BRCA-EU 6 79732697 79732697 insertion of <=200bp - T intron_variant BRCA-EU 6 79733508 79733508 single base substitution G C intron_variant BRCA-EU 6 79735062 79735062 deletion of <=200bp A - intron_variant BRCA-EU 6 79735907 79735907 single base substitution G A intron_variant BRCA-EU 6 79739047 79739047 single base substitution C T intron_variant BRCA-EU 6 79739505 79739505 single base substitution C G intron_variant BRCA-EU 6 79739888 79739888 single base substitution A C intron_variant BRCA-EU 6 79742837 79742837 single base substitution C T intron_variant BRCA-EU 6 79744344 79744344 single base substitution T C intron_variant BRCA-EU 6 79744661 79744661 single base substitution A C intron_variant BRCA-EU 6 79745136 79745136 single base substitution G C intron_variant BRCA-EU 6 79746391 79746391 single base substitution G T intron_variant BRCA-EU 6 79747107 79747107 single base substitution G C intron_variant BRCA-EU 6 79748422 79748422 single base substitution T A intron_variant BRCA-EU 6 79749518 79749518 single base substitution A T intron_variant BRCA-EU 6 79750462 79750462 insertion of <=200bp - A intron_variant BRCA-EU 6 79752329 79752329 single base substitution G A intron_variant BRCA-EU 6 79753155 79753155 single base substitution C G intron_variant BRCA-EU 6 79753471 79753471 single base substitution A C intron_variant BRCA-EU 6 79758117 79758117 single base substitution G T intron_variant BRCA-EU 6 79760187 79760187 single base substitution C G intron_variant BRCA-EU 6 79760524 79760524 single base substitution G A intron_variant BRCA-EU 6 79760918 79760918 single base substitution A G intron_variant BRCA-EU 6 79762266 79762266 single base substitution A C intron_variant BRCA-EU 6 79762416 79762416 single base substitution T A intron_variant BRCA-EU 6 79762510 79762510 single base substitution G C intron_variant BRCA-EU 6 79762882 79762882 single base substitution T A intron_variant BRCA-EU 6 79763166 79763166 single base substitution C G intron_variant BRCA-EU 6 79763724 79763724 deletion of <=200bp T - intron_variant BRCA-EU 6 79763894 79763894 deletion of <=200bp A - intron_variant BRCA-EU 6 79765879 79765879 single base substitution A G intron_variant BRCA-EU 6 79765899 79765899 single base substitution A G intron_variant BRCA-EU 6 79767341 79767341 single base substitution G T intron_variant BRCA-EU 6 79767575 79767575 single base substitution G C intron_variant BRCA-EU 6 79770023 79770023 single base substitution G T intron_variant BRCA-EU 6 79770807 79770807 single base substitution A C intron_variant BRCA-EU 6 79771241 79771241 single base substitution T A intron_variant BRCA-EU 6 79772404 79772404 single base substitution T A intron_variant BRCA-EU 6 79773517 79773517 single base substitution G T intron_variant BRCA-EU 6 79773532 79773532 single base substitution T A intron_variant BRCA-EU 6 79775032 79775032 single base substitution C G intron_variant BRCA-EU 6 79777295 79777295 single base substitution T A intron_variant BRCA-EU 6 79779047 79779047 single base substitution G A intron_variant BRCA-EU 6 79780023 79780023 single base substitution C G intron_variant BRCA-EU 6 79780857 79780857 single base substitution G C intron_variant BRCA-EU 6 79781612 79781612 single base substitution G A intron_variant BRCA-EU 6 79785297 79785297 single base substitution C A intron_variant BRCA-EU 6 79785812 79785812 single base substitution T C intron_variant BRCA-EU 6 79786552 79786552 single base substitution G C intron_variant BRCA-EU 6 79788350 79788350 single base substitution G C upstream_gene_variant BRCA-EU 6 79789207 79789207 single base substitution T G upstream_gene_variant BRCA-EU 6 79790107 79790107 single base substitution A T upstream_gene_variant BRCA-EU 6 79792175 79792175 single base substitution C G upstream_gene_variant BRCA-EU 6 79792923 79792923 single base substitution T A upstream_gene_variant BRCA-FR 6 79640635 79640635 single base substitution G C downstream_gene_variant BRCA-FR 6 79643246 79643246 single base substitution C T downstream_gene_variant BRCA-FR 6 79647613 79647613 single base substitution A G 3_prime_UTR_variant BRCA-FR 6 79647613 79647613 single base substitution A G downstream_gene_variant BRCA-FR 6 79661710 79661710 single base substitution C T intron_variant BRCA-FR 6 79666897 79666897 single base substitution G C exon_variant BRCA-FR 6 79666897 79666897 single base substitution G C intron_variant BRCA-FR 6 79670724 79670724 single base substitution G A intron_variant BRCA-FR 6 79682560 79682560 single base substitution G C intron_variant BRCA-FR 6 79688725 79688725 single base substitution G C intron_variant BRCA-FR 6 79690106 79690106 single base substitution G C intron_variant BRCA-FR 6 79690569 79690569 single base substitution C G intron_variant BRCA-FR 6 79693750 79693750 single base substitution G T intron_variant BRCA-FR 6 79693750 79693750 single base substitution G T upstream_gene_variant BRCA-FR 6 79701060 79701060 single base substitution G C intron_variant BRCA-FR 6 79702134 79702134 single base substitution T C intron_variant BRCA-FR 6 79707802 79707802 single base substitution G A intron_variant BRCA-FR 6 79709470 79709470 single base substitution A G intron_variant BRCA-FR 6 79720720 79720720 single base substitution G C intron_variant BRCA-FR 6 79722304 79722304 single base substitution T G intron_variant BRCA-FR 6 79724784 79724784 single base substitution G A intron_variant BRCA-FR 6 79729761 79729761 single base substitution T C intron_variant BRCA-FR 6 79733508 79733508 single base substitution G C intron_variant BRCA-FR 6 79734250 79734250 single base substitution G A intron_variant BRCA-FR 6 79745635 79745635 single base substitution G A intron_variant BRCA-FR 6 79753275 79753275 single base substitution A G intron_variant BRCA-FR 6 79756392 79756392 single base substitution G A intron_variant BRCA-FR 6 79766608 79766608 single base substitution G A intron_variant BRCA-FR 6 79788350 79788350 single base substitution G C upstream_gene_variant BRCA-UK 6 79650037 79650037 single base substitution C G 3_prime_UTR_variant BRCA-UK 6 79650037 79650037 single base substitution C G downstream_gene_variant BRCA-UK 6 79678444 79678444 single base substitution C T intron_variant BRCA-UK 6 79703872 79703872 single base substitution G C intron_variant BRCA-UK 6 79725451 79725451 single base substitution T C missense_variant M429V 1285A>G BRCA-UK 6 79729278 79729278 single base substitution T G intron_variant BRCA-UK 6 79744906 79744906 single base substitution C T intron_variant BRCA-US 6 79655835 79655835 single base substitution G A exon_variant BRCA-US 6 79655835 79655835 single base substitution G A stop_gained R1505* 4513C>T BRCA-US 6 79665349 79665351 deletion of <=200bp TTC - disruptive_inframe_deletion KK1277K BRCA-US 6 79665349 79665351 deletion of <=200bp TTC - exon_variant BRCA-US 6 79672892 79672892 single base substitution C T exon_variant BRCA-US 6 79672892 79672892 single base substitution C T missense_variant D1153N 3457G>A BRCA-US 6 79675691 79675691 single base substitution A G exon_variant BRCA-US 6 79675691 79675691 single base substitution A G synonymous_variant P1096P 3288T>C BRCA-US 6 79688311 79688311 single base substitution C T missense_variant E963K 2887G>A BRCA-US 6 79688311 79688311 single base substitution C T splice_region_variant BRCA-US 6 79692714 79692716 deletion of <=200bp TTC - inframe_deletion E886 BRCA-US 6 79692714 79692716 deletion of <=200bp TTC - upstream_gene_variant BRCA-US 6 79698009 79698009 deletion of <=200bp G - frameshift_variant Q793 BRCA-US 6 79698011 79698011 single base substitution T A missense_variant N792I 2375A>T BRCA-US 6 79698060 79698060 single base substitution C T missense_variant A776T 2326G>A BRCA-US 6 79725353 79725353 single base substitution G C synonymous_variant V461V 1383C>G BRCA-US 6 79725444 79725444 single base substitution G T missense_variant A431D 1292C>A BTCA-JP 6 79664387 79664387 single base substitution A G intron_variant BTCA-JP 6 79675841 79675841 single base substitution G A intron_variant BTCA-JP 6 79700788 79700788 single base substitution G A intron_variant BTCA-JP 6 79711711 79711711 single base substitution C T missense_variant G595D 1784G>A BTCA-JP 6 79752765 79752765 single base substitution T G intron_variant CESC-US 6 79650622 79650622 single base substitution C T exon_variant CESC-US 6 79650622 79650622 single base substitution C T missense_variant E1752K 5254G>A CESC-US 6 79655921 79655921 single base substitution G A exon_variant CESC-US 6 79655921 79655921 single base substitution G A missense_variant S1476F 4427C>T CLLE-ES 6 79651258 79651258 single base substitution T A intron_variant CLLE-ES 6 79657739 79657739 single base substitution G A intron_variant CLLE-ES 6 79675329 79675329 single base substitution A G intron_variant CLLE-ES 6 79689669 79689669 single base substitution C T intron_variant CLLE-ES 6 79702308 79702308 single base substitution T G intron_variant CLLE-ES 6 79714659 79714659 single base substitution T C intron_variant CLLE-ES 6 79768163 79768163 single base substitution C T intron_variant CLLE-ES 6 79784185 79784185 single base substitution G A intron_variant CLLE-ES 6 79788353 79788353 single base substitution A G upstream_gene_variant CLLE-ES 6 79791653 79791653 single base substitution G A upstream_gene_variant COAD-US 6 79650885 79650885 single base substitution T G exon_variant COAD-US 6 79650885 79650885 single base substitution T G missense_variant K1664T 4991A>C COAD-US 6 79655055 79655055 single base substitution G A exon_variant COAD-US 6 79655055 79655055 single base substitution G A missense_variant A1597V 4790C>T COAD-US 6 79655939 79655939 single base substitution T A exon_variant COAD-US 6 79655939 79655939 single base substitution T A missense_variant K1470I 4409A>T COAD-US 6 79656520 79656520 single base substitution T G exon_variant COAD-US 6 79656520 79656520 single base substitution T G missense_variant K1426N 4278A>C COAD-US 6 79656562 79656562 single base substitution A T exon_variant COAD-US 6 79656562 79656562 single base substitution A T synonymous_variant A1412A 4236T>A COAD-US 6 79656570 79656570 single base substitution G A exon_variant COAD-US 6 79656570 79656570 single base substitution G A synonymous_variant L1410L 4228C>T COAD-US 6 79664655 79664655 single base substitution C T exon_variant COAD-US 6 79664655 79664655 single base substitution C T missense_variant R1310H 3929G>A COAD-US 6 79665401 79665401 single base substitution T C exon_variant COAD-US 6 79665401 79665401 single base substitution T C splice_acceptor_variant COAD-US 6 79668299 79668299 single base substitution C T exon_variant COAD-US 6 79668299 79668299 single base substitution C T missense_variant M1225I 3675G>A COAD-US 6 79668321 79668321 deletion of <=200bp A - splice_region_variant COAD-US 6 79675701 79675701 single base substitution A G exon_variant COAD-US 6 79675701 79675701 single base substitution A G missense_variant L1093P 3278T>C COAD-US 6 79679609 79679609 single base substitution C T exon_variant COAD-US 6 79679609 79679609 single base substitution C T missense_variant D1050N 3148G>A COAD-US 6 79680570 79680570 single base substitution G A exon_variant COAD-US 6 79680570 79680570 single base substitution G A synonymous_variant V975V 2925C>T COAD-US 6 79707219 79707219 single base substitution C T missense_variant A705T 2113G>A COAD-US 6 79707227 79707227 single base substitution T A missense_variant H702L 2105A>T COAD-US 6 79725475 79725475 single base substitution T G missense_variant K421Q 1261A>C COAD-US 6 79735718 79735718 single base substitution C T missense_variant R255Q 764G>A COAD-US 6 79752673 79752673 single base substitution G A stop_gained R163* 487C>T COAD-US 6 79770387 79770387 single base substitution T G missense_variant K113T 338A>C COAD-US 6 79770396 79770396 single base substitution C T missense_variant R110H 329G>A COAD-US 6 79770437 79770437 single base substitution T C synonymous_variant G96G 288A>G COCA-CN 6 79650402 79650402 single base substitution G A 3_prime_UTR_variant COCA-CN 6 79650402 79650402 single base substitution G A exon_variant COCA-CN 6 79650648 79650648 single base substitution C T exon_variant COCA-CN 6 79650648 79650648 single base substitution C T missense_variant R1743Q 5228G>A COCA-CN 6 79651035 79651035 single base substitution T C exon_variant COCA-CN 6 79651035 79651035 single base substitution T C missense_variant N1614S 4841A>G COCA-CN 6 79653285 79653285 single base substitution C A intron_variant COCA-CN 6 79655139 79655139 single base substitution C G exon_variant COCA-CN 6 79655139 79655139 single base substitution C G missense_variant G1569A 4706G>C COCA-CN 6 79664748 79664748 single base substitution T C intron_variant COCA-CN 6 79668157 79668157 single base substitution A C exon_variant COCA-CN 6 79668157 79668157 single base substitution A C intron_variant COCA-CN 6 79668343 79668343 single base substitution T A intron_variant COCA-CN 6 79668903 79668903 single base substitution T C intron_variant COCA-CN 6 79675742 79675742 single base substitution G T exon_variant COCA-CN 6 79675742 79675742 single base substitution G T synonymous_variant A1079A 3237C>A COCA-CN 6 79679577 79679577 single base substitution A G exon_variant COCA-CN 6 79679577 79679577 single base substitution A G synonymous_variant D1060D 3180T>C COCA-CN 6 79681455 79681455 single base substitution T G intron_variant COCA-CN 6 79695139 79695139 single base substitution C T missense_variant E823K 2467G>A COCA-CN 6 79695139 79695139 single base substitution C T upstream_gene_variant COCA-CN 6 79707060 79707060 single base substitution G T intron_variant COCA-CN 6 79707352 79707352 single base substitution G T intron_variant COCA-CN 6 79711522 79711522 single base substitution C T intron_variant COCA-CN 6 79713340 79713340 single base substitution T G intron_variant COCA-CN 6 79726176 79726176 single base substitution T G intron_variant COCA-CN 6 79726309 79726309 single base substitution C T missense_variant R396Q 1187G>A COCA-CN 6 79726310 79726310 single base substitution G A stop_gained R396* 1186C>T COCA-CN 6 79726327 79726327 single base substitution C T missense_variant R390H 1169G>A COCA-CN 6 79726430 79726430 single base substitution G T intron_variant COCA-CN 6 79727178 79727178 single base substitution A C intron_variant COCA-CN 6 79735398 79735398 single base substitution C A intron_variant COCA-CN 6 79741642 79741642 single base substitution C G intron_variant COCA-CN 6 79748386 79748386 single base substitution T C intron_variant COCA-CN 6 79764072 79764072 single base substitution G A intron_variant COCA-CN 6 79782209 79782209 single base substitution C T intron_variant COCA-CN 6 79787127 79787127 single base substitution G A intron_variant EOPC-DE 6 79665631 79665631 single base substitution T C exon_variant EOPC-DE 6 79665631 79665631 single base substitution T C intron_variant ESAD-UK 6 79643806 79643806 single base substitution G A downstream_gene_variant ESAD-UK 6 79643863 79643863 single base substitution T C downstream_gene_variant ESAD-UK 6 79644561 79644561 single base substitution G C downstream_gene_variant ESAD-UK 6 79647234 79647234 single base substitution G A 3_prime_UTR_variant ESAD-UK 6 79647234 79647234 single base substitution G A downstream_gene_variant ESAD-UK 6 79649345 79649345 single base substitution C T 3_prime_UTR_variant ESAD-UK 6 79649345 79649345 single base substitution C T downstream_gene_variant ESAD-UK 6 79649438 79649438 single base substitution A C 3_prime_UTR_variant ESAD-UK 6 79649438 79649438 single base substitution A C downstream_gene_variant ESAD-UK 6 79652734 79652734 single base substitution C A intron_variant ESAD-UK 6 79661803 79661803 single base substitution G T intron_variant ESAD-UK 6 79665208 79665208 single base substitution T A intron_variant ESAD-UK 6 79665209 79665209 single base substitution T A intron_variant ESAD-UK 6 79665897 79665897 single base substitution G T exon_variant ESAD-UK 6 79665897 79665897 single base substitution G T intron_variant ESAD-UK 6 79666005 79666005 single base substitution T C exon_variant ESAD-UK 6 79666005 79666005 single base substitution T C intron_variant ESAD-UK 6 79667083 79667083 single base substitution A G exon_variant ESAD-UK 6 79667083 79667083 single base substitution A G intron_variant ESAD-UK 6 79668428 79668428 single base substitution A T intron_variant ESAD-UK 6 79669442 79669442 single base substitution T C intron_variant ESAD-UK 6 79671674 79671674 single base substitution G C intron_variant ESAD-UK 6 79673077 79673077 single base substitution G T intron_variant ESAD-UK 6 79674760 79674760 single base substitution T C intron_variant ESAD-UK 6 79674793 79674793 single base substitution C T intron_variant ESAD-UK 6 79677395 79677395 single base substitution C G intron_variant ESAD-UK 6 79678484 79678484 single base substitution T A intron_variant ESAD-UK 6 79680294 79680294 single base substitution T A intron_variant ESAD-UK 6 79688611 79688611 single base substitution C T intron_variant ESAD-UK 6 79689505 79689505 single base substitution T A intron_variant ESAD-UK 6 79689913 79689913 single base substitution C T intron_variant ESAD-UK 6 79690518 79690518 single base substitution T G intron_variant ESAD-UK 6 79694410 79694410 single base substitution G T intron_variant ESAD-UK 6 79694410 79694410 single base substitution G T upstream_gene_variant ESAD-UK 6 79695368 79695368 single base substitution G A intron_variant ESAD-UK 6 79695368 79695368 single base substitution G A upstream_gene_variant ESAD-UK 6 79695451 79695451 single base substitution T C intron_variant ESAD-UK 6 79695451 79695451 single base substitution T C upstream_gene_variant ESAD-UK 6 79695921 79695921 single base substitution C G intron_variant ESAD-UK 6 79695921 79695921 single base substitution C G upstream_gene_variant ESAD-UK 6 79696216 79696216 insertion of <=200bp - T intron_variant ESAD-UK 6 79696216 79696216 insertion of <=200bp - T upstream_gene_variant ESAD-UK 6 79698221 79698221 single base substitution G A intron_variant ESAD-UK 6 79698803 79698803 insertion of <=200bp - A intron_variant ESAD-UK 6 79699326 79699326 single base substitution C T intron_variant ESAD-UK 6 79703249 79703249 single base substitution A C intron_variant ESAD-UK 6 79703862 79703862 single base substitution C T intron_variant ESAD-UK 6 79703897 79703897 single base substitution G A intron_variant ESAD-UK 6 79704044 79704044 single base substitution C T intron_variant ESAD-UK 6 79705199 79705199 single base substitution C A intron_variant ESAD-UK 6 79705282 79705282 single base substitution G C intron_variant ESAD-UK 6 79708442 79708442 single base substitution A G intron_variant ESAD-UK 6 79709696 79709696 deletion of <=200bp A - intron_variant ESAD-UK 6 79709750 79709750 single base substitution T G intron_variant ESAD-UK 6 79709854 79709854 single base substitution G C intron_variant ESAD-UK 6 79710080 79710080 single base substitution T G intron_variant ESAD-UK 6 79711301 79711301 single base substitution G A intron_variant ESAD-UK 6 79711554 79711554 single base substitution A C intron_variant ESAD-UK 6 79713335 79713335 single base substitution G T intron_variant ESAD-UK 6 79713607 79713607 single base substitution T G intron_variant ESAD-UK 6 79714111 79714111 single base substitution C G intron_variant ESAD-UK 6 79715546 79715546 single base substitution G A intron_variant ESAD-UK 6 79721097 79721097 single base substitution T G intron_variant ESAD-UK 6 79725167 79725167 single base substitution A G intron_variant ESAD-UK 6 79725361 79725361 single base substitution T C missense_variant I459V 1375A>G ESAD-UK 6 79726946 79726946 single base substitution G C intron_variant ESAD-UK 6 79732548 79732548 single base substitution C A intron_variant ESAD-UK 6 79737361 79737361 single base substitution T G intron_variant ESAD-UK 6 79737574 79737574 single base substitution T C intron_variant ESAD-UK 6 79738792 79738792 single base substitution C A intron_variant ESAD-UK 6 79739756 79739756 single base substitution A T intron_variant ESAD-UK 6 79740010 79740010 single base substitution C T intron_variant ESAD-UK 6 79741687 79741687 single base substitution A G intron_variant ESAD-UK 6 79741994 79741994 single base substitution A T intron_variant ESAD-UK 6 79742799 79742799 single base substitution T A intron_variant ESAD-UK 6 79744331 79744331 single base substitution C T intron_variant ESAD-UK 6 79744862 79744862 single base substitution G C intron_variant ESAD-UK 6 79747492 79747492 single base substitution G C intron_variant ESAD-UK 6 79748657 79748657 single base substitution A G intron_variant ESAD-UK 6 79749273 79749273 single base substitution C A intron_variant ESAD-UK 6 79752541 79752541 single base substitution T A intron_variant ESAD-UK 6 79754588 79754588 single base substitution G A intron_variant ESAD-UK 6 79755472 79755472 single base substitution G T intron_variant ESAD-UK 6 79759666 79759666 single base substitution G A intron_variant ESAD-UK 6 79760673 79760673 single base substitution A T intron_variant ESAD-UK 6 79762191 79762191 single base substitution A G intron_variant ESAD-UK 6 79762526 79762526 single base substitution G A intron_variant ESAD-UK 6 79763724 79763724 deletion of <=200bp T - intron_variant ESAD-UK 6 79763894 79763894 deletion of <=200bp A - intron_variant ESAD-UK 6 79764024 79764024 deletion of <=200bp A - intron_variant ESAD-UK 6 79764106 79764106 single base substitution G A intron_variant ESAD-UK 6 79764385 79764385 deletion of <=200bp A - intron_variant ESAD-UK 6 79767335 79767335 single base substitution T C intron_variant ESAD-UK 6 79771861 79771861 single base substitution T C intron_variant ESAD-UK 6 79775712 79775712 single base substitution T C intron_variant ESAD-UK 6 79775768 79775768 single base substitution T A intron_variant ESAD-UK 6 79778519 79778519 single base substitution G C intron_variant ESAD-UK 6 79780631 79780631 single base substitution G A intron_variant ESAD-UK 6 79784831 79784831 single base substitution A G intron_variant ESAD-UK 6 79787647 79787647 single base substitution G A intron_variant ESAD-UK 6 79788672 79788672 single base substitution G A upstream_gene_variant ESAD-UK 6 79789556 79789556 single base substitution G C upstream_gene_variant ESAD-UK 6 79791716 79791716 single base substitution C T upstream_gene_variant ESCA-CN 6 79657357 79657357 single base substitution G C exon_variant ESCA-CN 6 79657357 79657357 single base substitution G C missense_variant P1397A 4189C>G ESCA-CN 6 79735722 79735722 single base substitution G C missense_variant L254V 760C>G ESCA-CN 6 79752440 79752440 single base substitution C A intron_variant KIRC-US 6 79650693 79650693 single base substitution T G exon_variant KIRC-US 6 79650693 79650693 single base substitution T G missense_variant D1728A 5183A>C KIRC-US 6 79708068 79708068 single base substitution G A synonymous_variant I640I 1920C>T KIRP-US 6 79724879 79724879 single base substitution G A missense_variant L482F 1444C>T LAML-KR 6 79670184 79670184 single base substitution C T intron_variant LAML-KR 6 79672881 79672881 single base substitution C T exon_variant LAML-KR 6 79672881 79672881 single base substitution C T stop_gained W1156* 3468G>A LAML-KR 6 79675701 79675701 single base substitution A G exon_variant LAML-KR 6 79675701 79675701 single base substitution A G missense_variant L1093P 3278T>C LAML-KR 6 79707051 79707051 single base substitution A G intron_variant LAML-KR 6 79735773 79735773 single base substitution T A missense_variant N237Y 709A>T LGG-US 6 79650981 79650981 single base substitution G C exon_variant LGG-US 6 79650981 79650981 single base substitution G C stop_gained S1632* 4895C>G LICA-CN 6 79650765 79650765 single base substitution T C exon_variant LICA-CN 6 79650765 79650765 single base substitution T C missense_variant D1704G 5111A>G LICA-CN 6 79735800 79735800 single base substitution T G missense_variant I228L 682A>C LICA-FR 6 79652840 79652840 single base substitution T A intron_variant LICA-FR 6 79671446 79671446 single base substitution A G exon_variant LICA-FR 6 79671446 79671446 single base substitution A G missense_variant L1206P 3617T>C LICA-FR 6 79673585 79673585 single base substitution A T intron_variant LICA-FR 6 79684891 79684891 single base substitution C G intron_variant LICA-FR 6 79687966 79687966 deletion of <=200bp T - intron_variant LICA-FR 6 79696984 79696984 single base substitution T C intron_variant LICA-FR 6 79696984 79696984 single base substitution T C upstream_gene_variant LIHC-US 6 79657378 79657378 single base substitution T A exon_variant LIHC-US 6 79657378 79657378 single base substitution T A missense_variant S1390C 4168A>T LIHC-US 6 79688417 79688417 single base substitution C G exon_variant LIHC-US 6 79688417 79688417 single base substitution C G synonymous_variant V927V 2781G>C LIHC-US 6 79688429 79688429 single base substitution C A splice_acceptor_variant LIHC-US 6 79692705 79692705 single base substitution T C synonymous_variant K889K 2667A>G LIHC-US 6 79692705 79692705 single base substitution T C upstream_gene_variant LIHC-US 6 79770201 79770201 single base substitution T A missense_variant S145C 433A>T LINC-JP 6 79641785 79641785 single base substitution G A downstream_gene_variant LINC-JP 6 79649385 79649385 single base substitution C G 3_prime_UTR_variant LINC-JP 6 79649385 79649385 single base substitution C G downstream_gene_variant LINC-JP 6 79654996 79654996 single base substitution A C intron_variant LINC-JP 6 79655202 79655202 single base substitution G C exon_variant LINC-JP 6 79655202 79655202 single base substitution G C missense_variant S1548C 4643C>G LINC-JP 6 79655932 79655932 single base substitution T A exon_variant LINC-JP 6 79655932 79655932 single base substitution T A missense_variant E1472D 4416A>T LINC-JP 6 79663060 79663060 single base substitution A G intron_variant LINC-JP 6 79675606 79675606 deletion of <=200bp A - intron_variant LINC-JP 6 79679747 79679747 single base substitution C T intron_variant LINC-JP 6 79681167 79681167 single base substitution T C intron_variant LINC-JP 6 79692484 79692484 single base substitution T A intron_variant LINC-JP 6 79692884 79692884 single base substitution G A intron_variant LINC-JP 6 79692884 79692884 single base substitution G A upstream_gene_variant LINC-JP 6 79693855 79693855 single base substitution C T intron_variant LINC-JP 6 79693855 79693855 single base substitution C T upstream_gene_variant LINC-JP 6 79693856 79693856 single base substitution A G intron_variant LINC-JP 6 79693856 79693856 single base substitution A G upstream_gene_variant LINC-JP 6 79697876 79697876 single base substitution A C intron_variant LINC-JP 6 79698453 79698454 deletion of <=200bp TT - intron_variant LINC-JP 6 79711666 79711666 single base substitution T A missense_variant E610V 1829A>T LINC-JP 6 79716672 79716672 single base substitution T C intron_variant LINC-JP 6 79718483 79718483 single base substitution C A intron_variant LINC-JP 6 79721547 79721547 insertion of <=200bp - A intron_variant LINC-JP 6 79735380 79735380 single base substitution C T intron_variant LINC-JP 6 79749355 79749355 single base substitution T C intron_variant LINC-JP 6 79782209 79782209 single base substitution C T intron_variant LINC-JP 6 79786403 79786403 single base substitution A C intron_variant LINC-JP 6 79786962 79786962 single base substitution C T intron_variant LINC-JP 6 79788384 79788384 single base substitution G T upstream_gene_variant LINC-JP 6 79789473 79789473 single base substitution T A upstream_gene_variant LIRI-JP 6 79641235 79641235 single base substitution T C downstream_gene_variant LIRI-JP 6 79642915 79642915 single base substitution G T downstream_gene_variant LIRI-JP 6 79649453 79649453 single base substitution C A 3_prime_UTR_variant LIRI-JP 6 79649453 79649453 single base substitution C A downstream_gene_variant LIRI-JP 6 79649855 79649858 deletion of <=200bp TAAT - 3_prime_UTR_variant LIRI-JP 6 79649855 79649858 deletion of <=200bp TAAT - downstream_gene_variant LIRI-JP 6 79650704 79650704 single base substitution T C exon_variant LIRI-JP 6 79650704 79650704 single base substitution T C synonymous_variant K1724K 5172A>G LIRI-JP 6 79651468 79651468 single base substitution T A intron_variant LIRI-JP 6 79653125 79653125 single base substitution A C intron_variant LIRI-JP 6 79654068 79654068 single base substitution G C intron_variant LIRI-JP 6 79657987 79657987 single base substitution T C intron_variant LIRI-JP 6 79660789 79660789 single base substitution A C intron_variant LIRI-JP 6 79662906 79662906 single base substitution C A intron_variant LIRI-JP 6 79663569 79663569 single base substitution C T intron_variant LIRI-JP 6 79664655 79664655 single base substitution C T exon_variant LIRI-JP 6 79664655 79664655 single base substitution C T missense_variant R1310H 3929G>A LIRI-JP 6 79667777 79667777 single base substitution A G exon_variant LIRI-JP 6 79667777 79667777 single base substitution A G intron_variant LIRI-JP 6 79668075 79668075 single base substitution A G exon_variant LIRI-JP 6 79668075 79668075 single base substitution A G intron_variant LIRI-JP 6 79668124 79668124 single base substitution T C exon_variant LIRI-JP 6 79668124 79668124 single base substitution T C intron_variant LIRI-JP 6 79670648 79670648 single base substitution T C intron_variant LIRI-JP 6 79674244 79674244 single base substitution C G intron_variant LIRI-JP 6 79674518 79674518 single base substitution T C intron_variant LIRI-JP 6 79681282 79681282 single base substitution C G intron_variant LIRI-JP 6 79688217 79688217 single base substitution G C intron_variant LIRI-JP 6 79689780 79689780 single base substitution G A intron_variant LIRI-JP 6 79692519 79692519 insertion of <=200bp - T intron_variant LIRI-JP 6 79692872 79692872 single base substitution A T intron_variant LIRI-JP 6 79692872 79692872 single base substitution A T upstream_gene_variant LIRI-JP 6 79693965 79693965 single base substitution T C intron_variant LIRI-JP 6 79693965 79693965 single base substitution T C upstream_gene_variant LIRI-JP 6 79695666 79695666 single base substitution T C intron_variant LIRI-JP 6 79695666 79695666 single base substitution T C upstream_gene_variant LIRI-JP 6 79697684 79697684 single base substitution A G intron_variant LIRI-JP 6 79699945 79699945 single base substitution T C intron_variant LIRI-JP 6 79700157 79700157 single base substitution T C intron_variant LIRI-JP 6 79700923 79700923 single base substitution T A intron_variant LIRI-JP 6 79701294 79701294 single base substitution T A intron_variant LIRI-JP 6 79707079 79707079 single base substitution C T intron_variant LIRI-JP 6 79708070 79708070 single base substitution T C missense_variant I640V 1918A>G LIRI-JP 6 79711679 79711679 single base substitution C G missense_variant V606L 1816G>C LIRI-JP 6 79712362 79712362 single base substitution T C intron_variant LIRI-JP 6 79712367 79712367 single base substitution A T intron_variant LIRI-JP 6 79713246 79713246 single base substitution T C intron_variant LIRI-JP 6 79713940 79713940 single base substitution A G intron_variant LIRI-JP 6 79714485 79714485 single base substitution T C intron_variant LIRI-JP 6 79715086 79715086 single base substitution G C intron_variant LIRI-JP 6 79718094 79718094 single base substitution T C intron_variant LIRI-JP 6 79718902 79718902 single base substitution T C intron_variant LIRI-JP 6 79719105 79719105 single base substitution T C intron_variant LIRI-JP 6 79719178 79719178 single base substitution A G intron_variant LIRI-JP 6 79722780 79722780 single base substitution T C intron_variant LIRI-JP 6 79725162 79725162 single base substitution A G intron_variant LIRI-JP 6 79725589 79725589 single base substitution C A intron_variant LIRI-JP 6 79728429 79728429 single base substitution T C intron_variant LIRI-JP 6 79730255 79730255 single base substitution C A intron_variant LIRI-JP 6 79731691 79731691 single base substitution T A intron_variant LIRI-JP 6 79732888 79732888 single base substitution T C intron_variant LIRI-JP 6 79733344 79733344 single base substitution T C intron_variant LIRI-JP 6 79735395 79735395 single base substitution C T intron_variant LIRI-JP 6 79737363 79737363 single base substitution T C intron_variant LIRI-JP 6 79737881 79737881 single base substitution G A intron_variant LIRI-JP 6 79738708 79738708 single base substitution G C intron_variant LIRI-JP 6 79738873 79738873 single base substitution A T intron_variant LIRI-JP 6 79740343 79740343 single base substitution C G intron_variant LIRI-JP 6 79740715 79740715 single base substitution T C intron_variant LIRI-JP 6 79741181 79741181 single base substitution T A intron_variant LIRI-JP 6 79741191 79741191 single base substitution C A intron_variant LIRI-JP 6 79742301 79742301 single base substitution T C intron_variant LIRI-JP 6 79743359 79743359 single base substitution T C intron_variant LIRI-JP 6 79744457 79744457 single base substitution G T intron_variant LIRI-JP 6 79746307 79746307 single base substitution A G intron_variant LIRI-JP 6 79747588 79747588 single base substitution T A intron_variant LIRI-JP 6 79748871 79748871 single base substitution T C intron_variant LIRI-JP 6 79749631 79749631 single base substitution T C intron_variant LIRI-JP 6 79750331 79750331 single base substitution C T intron_variant LIRI-JP 6 79750972 79750972 single base substitution C T intron_variant LIRI-JP 6 79753944 79753944 single base substitution T C intron_variant LIRI-JP 6 79754424 79754424 single base substitution C T intron_variant LIRI-JP 6 79759144 79759144 single base substitution T C intron_variant LIRI-JP 6 79760697 79760697 single base substitution A G intron_variant LIRI-JP 6 79760720 79760720 insertion of <=200bp - AC intron_variant LIRI-JP 6 79765387 79765387 single base substitution C T intron_variant LIRI-JP 6 79768934 79768934 single base substitution A G intron_variant LIRI-JP 6 79770063 79770063 single base substitution T C intron_variant LIRI-JP 6 79771503 79771503 single base substitution C T intron_variant LIRI-JP 6 79771639 79771639 single base substitution T C intron_variant LIRI-JP 6 79776555 79776555 single base substitution G C intron_variant LIRI-JP 6 79777623 79777623 single base substitution G A intron_variant LIRI-JP 6 79777779 79777779 single base substitution T C intron_variant LIRI-JP 6 79780340 79780340 single base substitution G C intron_variant LIRI-JP 6 79781128 79781128 single base substitution T C intron_variant LIRI-JP 6 79784510 79784510 single base substitution C T intron_variant LIRI-JP 6 79785245 79785245 single base substitution C T intron_variant LIRI-JP 6 79786668 79786668 single base substitution A G intron_variant LIRI-JP 6 79787081 79787081 single base substitution T C intron_variant LIRI-JP 6 79790412 79790412 single base substitution C G upstream_gene_variant LIRI-JP 6 79792615 79792615 single base substitution T C upstream_gene_variant LUSC-KR 6 79642156 79642156 single base substitution G T downstream_gene_variant LUSC-KR 6 79642954 79642954 single base substitution C T downstream_gene_variant LUSC-KR 6 79649564 79649564 single base substitution T A 3_prime_UTR_variant LUSC-KR 6 79649564 79649564 single base substitution T A downstream_gene_variant LUSC-KR 6 79650779 79650779 single base substitution A G exon_variant LUSC-KR 6 79650779 79650779 single base substitution A G synonymous_variant N1699N 5097T>C LUSC-KR 6 79657797 79657797 single base substitution C A intron_variant LUSC-KR 6 79675275 79675275 single base substitution A G intron_variant LUSC-KR 6 79685645 79685645 single base substitution T A intron_variant LUSC-KR 6 79686757 79686757 single base substitution G T intron_variant LUSC-KR 6 79686853 79686853 single base substitution A G intron_variant LUSC-KR 6 79686912 79686912 single base substitution T C intron_variant LUSC-KR 6 79688652 79688652 single base substitution G T intron_variant LUSC-KR 6 79716823 79716823 single base substitution T G intron_variant LUSC-KR 6 79722730 79722730 single base substitution C T intron_variant LUSC-KR 6 79725667 79725667 single base substitution G A intron_variant LUSC-KR 6 79742348 79742348 single base substitution A G intron_variant LUSC-KR 6 79750128 79750128 single base substitution A G intron_variant LUSC-KR 6 79755890 79755890 single base substitution C A intron_variant LUSC-KR 6 79756351 79756351 single base substitution T A intron_variant LUSC-KR 6 79756360 79756360 single base substitution G T intron_variant LUSC-KR 6 79759942 79759942 single base substitution C T intron_variant LUSC-KR 6 79760057 79760057 single base substitution G C intron_variant LUSC-KR 6 79760963 79760963 single base substitution A G intron_variant LUSC-KR 6 79768496 79768496 single base substitution C G intron_variant LUSC-KR 6 79769893 79769893 single base substitution G T intron_variant LUSC-KR 6 79771223 79771223 single base substitution C G intron_variant LUSC-KR 6 79782762 79782762 single base substitution C G intron_variant LUSC-KR 6 79787760 79787760 single base substitution G A missense_variant S9L 26C>T LUSC-KR 6 79789379 79789379 single base substitution T C upstream_gene_variant LUSC-US 6 79650528 79650528 single base substitution G T exon_variant LUSC-US 6 79650528 79650528 single base substitution G T missense_variant S1783Y 5348C>A LUSC-US 6 79650830 79650830 single base substitution G C exon_variant LUSC-US 6 79650830 79650830 single base substitution G C missense_variant I1682M 5046C>G LUSC-US 6 79655828 79655828 single base substitution C T exon_variant LUSC-US 6 79655828 79655828 single base substitution C T missense_variant R1507K 4520G>A LUSC-US 6 79672829 79672829 single base substitution G T exon_variant LUSC-US 6 79672829 79672829 single base substitution G T missense_variant Q1174K 3520C>A LUSC-US 6 79672925 79672925 single base substitution C A exon_variant LUSC-US 6 79672925 79672925 single base substitution C A missense_variant G1142C 3424G>T LUSC-US 6 79688325 79688325 single base substitution G T exon_variant LUSC-US 6 79688325 79688325 single base substitution G T missense_variant P958Q 2873C>A LUSC-US 6 79707136 79707136 single base substitution T A synonymous_variant V732V 2196A>T LUSC-US 6 79725400 79725400 single base substitution T C missense_variant M446V 1336A>G LUSC-US 6 79752705 79752705 single base substitution G A missense_variant S152L 455C>T MALY-DE 6 79646081 79646081 single base substitution G A 3_prime_UTR_variant MALY-DE 6 79646081 79646081 single base substitution G A downstream_gene_variant MALY-DE 6 79657722 79657722 single base substitution T G intron_variant MALY-DE 6 79663520 79663520 single base substitution C G intron_variant MALY-DE 6 79669123 79669123 single base substitution T A intron_variant MALY-DE 6 79675483 79675483 single base substitution T A splice_acceptor_variant MALY-DE 6 79676569 79676569 single base substitution T G intron_variant MALY-DE 6 79679519 79679519 single base substitution C A intron_variant MALY-DE 6 79688924 79688924 single base substitution A G intron_variant MALY-DE 6 79693046 79693046 single base substitution T G intron_variant MALY-DE 6 79693046 79693046 single base substitution T G upstream_gene_variant MALY-DE 6 79697751 79697751 single base substitution T C intron_variant MALY-DE 6 79704581 79704581 single base substitution C T intron_variant MALY-DE 6 79712501 79712501 single base substitution T C intron_variant MALY-DE 6 79715963 79715963 single base substitution T A intron_variant MALY-DE 6 79717337 79717337 single base substitution T C intron_variant MALY-DE 6 79721847 79721847 single base substitution T C intron_variant MALY-DE 6 79726604 79726604 single base substitution A C intron_variant MALY-DE 6 79734480 79734480 single base substitution A G intron_variant MALY-DE 6 79735637 79735637 single base substitution T A intron_variant MALY-DE 6 79735873 79735873 single base substitution A C missense_variant D203E 609T>G MALY-DE 6 79746354 79746354 single base substitution G A intron_variant MALY-DE 6 79746474 79746474 single base substitution T C intron_variant MALY-DE 6 79751509 79751509 single base substitution G A intron_variant MALY-DE 6 79752557 79752557 single base substitution T A splice_region_variant MALY-DE 6 79752558 79752558 single base substitution A T splice_donor_variant MALY-DE 6 79753178 79753178 single base substitution A C intron_variant MALY-DE 6 79753539 79753539 single base substitution A G intron_variant MALY-DE 6 79756955 79756955 single base substitution A G intron_variant MALY-DE 6 79757083 79757083 single base substitution A T intron_variant MALY-DE 6 79757904 79757904 single base substitution A C intron_variant MALY-DE 6 79758032 79758032 single base substitution A C intron_variant MALY-DE 6 79758089 79758089 single base substitution A T intron_variant MALY-DE 6 79763133 79763133 single base substitution A C intron_variant MALY-DE 6 79770414 79770414 single base substitution C A missense_variant G104V 311G>T MALY-DE 6 79775408 79775408 single base substitution A T intron_variant MALY-DE 6 79779344 79779344 single base substitution T C intron_variant MALY-DE 6 79779862 79779862 single base substitution A C intron_variant MALY-DE 6 79780564 79780564 single base substitution A T intron_variant MALY-DE 6 79788752 79788752 single base substitution C G upstream_gene_variant MALY-DE 6 79788766 79788766 single base substitution T A upstream_gene_variant MALY-DE 6 79789492 79789492 insertion of <=200bp - A upstream_gene_variant MALY-DE 6 79791249 79791249 single base substitution A G upstream_gene_variant MELA-AU 6 79640688 79640688 single base substitution A T downstream_gene_variant MELA-AU 6 79640828 79640828 single base substitution T C downstream_gene_variant MELA-AU 6 79641334 79641334 single base substitution A G downstream_gene_variant MELA-AU 6 79641576 79641576 single base substitution G A downstream_gene_variant MELA-AU 6 79642188 79642188 single base substitution G A downstream_gene_variant MELA-AU 6 79642306 79642306 single base substitution T C downstream_gene_variant MELA-AU 6 79642914 79642914 single base substitution G A downstream_gene_variant MELA-AU 6 79643722 79643722 single base substitution A G downstream_gene_variant MELA-AU 6 79644452 79644452 single base substitution A G downstream_gene_variant MELA-AU 6 79644990 79644990 single base substitution G C downstream_gene_variant MELA-AU 6 79645036 79645036 single base substitution G A downstream_gene_variant MELA-AU 6 79645128 79645128 single base substitution T C downstream_gene_variant MELA-AU 6 79645530 79645530 single base substitution T C downstream_gene_variant MELA-AU 6 79646613 79646613 single base substitution G A 3_prime_UTR_variant MELA-AU 6 79646613 79646613 single base substitution G A downstream_gene_variant MELA-AU 6 79647174 79647174 single base substitution T G 3_prime_UTR_variant MELA-AU 6 79647174 79647174 single base substitution T G downstream_gene_variant MELA-AU 6 79649276 79649276 single base substitution A T 3_prime_UTR_variant MELA-AU 6 79649276 79649276 single base substitution A T downstream_gene_variant MELA-AU 6 79649776 79649776 single base substitution A T 3_prime_UTR_variant MELA-AU 6 79649776 79649776 single base substitution A T downstream_gene_variant MELA-AU 6 79649792 79649792 single base substitution T C 3_prime_UTR_variant MELA-AU 6 79649792 79649792 single base substitution T C downstream_gene_variant MELA-AU 6 79649891 79649891 single base substitution G A 3_prime_UTR_variant MELA-AU 6 79649891 79649891 single base substitution G A downstream_gene_variant MELA-AU 6 79650562 79650562 single base substitution C T exon_variant MELA-AU 6 79650562 79650562 single base substitution C T missense_variant G1772S 5314G>A MELA-AU 6 79650872 79650872 single base substitution A G exon_variant MELA-AU 6 79650872 79650872 single base substitution A G synonymous_variant Y1668Y 5004T>C MELA-AU 6 79652021 79652021 single base substitution G A intron_variant MELA-AU 6 79652066 79652066 single base substitution G A intron_variant MELA-AU 6 79652096 79652096 single base substitution G A intron_variant MELA-AU 6 79652731 79652731 single base substitution G A intron_variant MELA-AU 6 79652808 79652808 single base substitution A G intron_variant MELA-AU 6 79653345 79653345 single base substitution G A intron_variant MELA-AU 6 79654718 79654718 single base substitution T C intron_variant MELA-AU 6 79654859 79654859 single base substitution G A intron_variant MELA-AU 6 79655180 79655180 single base substitution C G exon_variant MELA-AU 6 79655180 79655180 single base substitution C G missense_variant L1555F 4665G>C MELA-AU 6 79655834 79655834 single base substitution C T exon_variant MELA-AU 6 79655834 79655834 single base substitution C T missense_variant R1505Q 4514G>A MELA-AU 6 79656107 79656107 single base substitution T A intron_variant MELA-AU 6 79656179 79656179 single base substitution G A intron_variant MELA-AU 6 79656948 79656948 single base substitution G A intron_variant MELA-AU 6 79657839 79657839 single base substitution T C intron_variant MELA-AU 6 79658113 79658113 single base substitution C T intron_variant MELA-AU 6 79659108 79659108 single base substitution A G intron_variant MELA-AU 6 79659314 79659314 single base substitution G A intron_variant MELA-AU 6 79660235 79660235 single base substitution T C intron_variant MELA-AU 6 79660782 79660782 single base substitution T C intron_variant MELA-AU 6 79661021 79661021 single base substitution T A intron_variant MELA-AU 6 79661260 79661260 single base substitution C T intron_variant MELA-AU 6 79661933 79661933 single base substitution T G intron_variant MELA-AU 6 79663222 79663222 single base substitution G A intron_variant MELA-AU 6 79663976 79663976 single base substitution G A intron_variant MELA-AU 6 79665159 79665159 single base substitution A T intron_variant MELA-AU 6 79666379 79666379 single base substitution C T exon_variant MELA-AU 6 79666379 79666379 single base substitution C T intron_variant MELA-AU 6 79667595 79667595 single base substitution G T exon_variant MELA-AU 6 79667595 79667595 single base substitution G T intron_variant MELA-AU 6 79667650 79667650 single base substitution G A exon_variant MELA-AU 6 79667650 79667650 single base substitution G A intron_variant MELA-AU 6 79668014 79668014 single base substitution G A exon_variant MELA-AU 6 79668014 79668014 single base substitution G A intron_variant MELA-AU 6 79668177 79668177 single base substitution G A exon_variant MELA-AU 6 79668177 79668177 single base substitution G A intron_variant MELA-AU 6 79668882 79668882 single base substitution A T intron_variant MELA-AU 6 79669321 79669346 deletion of <=200bp AATACATTGAAGTCATCATTGTATTG - intron_variant MELA-AU 6 79669584 79669584 single base substitution A G intron_variant MELA-AU 6 79669637 79669637 single base substitution C T intron_variant MELA-AU 6 79669938 79669938 single base substitution T C intron_variant MELA-AU 6 79670198 79670198 single base substitution A G intron_variant MELA-AU 6 79670484 79670484 single base substitution C T intron_variant MELA-AU 6 79671145 79671145 single base substitution G A intron_variant MELA-AU 6 79671503 79671503 single base substitution G A exon_variant MELA-AU 6 79671503 79671503 single base substitution G A missense_variant P1187L 3560C>T MELA-AU 6 79671883 79671883 single base substitution A G intron_variant MELA-AU 6 79671895 79671895 single base substitution T G intron_variant MELA-AU 6 79671976 79671976 single base substitution G A intron_variant MELA-AU 6 79672725 79672725 single base substitution A G intron_variant MELA-AU 6 79672936 79672936 single base substitution G A exon_variant MELA-AU 6 79672936 79672936 single base substitution G A missense_variant P1138L 3413C>T MELA-AU 6 79673408 79673408 single base substitution A T intron_variant MELA-AU 6 79673842 79673842 single base substitution A G intron_variant MELA-AU 6 79673896 79673896 single base substitution T C intron_variant MELA-AU 6 79674940 79674940 single base substitution G A intron_variant MELA-AU 6 79675041 79675041 single base substitution G A intron_variant MELA-AU 6 79677668 79677669 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 79678912 79678912 single base substitution A T intron_variant MELA-AU 6 79679171 79679177 deletion of <=200bp AATAGGA - intron_variant MELA-AU 6 79679226 79679226 single base substitution C T intron_variant MELA-AU 6 79680223 79680223 single base substitution G A intron_variant MELA-AU 6 79680232 79680232 single base substitution G A intron_variant MELA-AU 6 79681574 79681574 single base substitution G A intron_variant MELA-AU 6 79681657 79681657 single base substitution G A intron_variant MELA-AU 6 79682217 79682217 single base substitution C T intron_variant MELA-AU 6 79682283 79682283 single base substitution G A intron_variant MELA-AU 6 79683718 79683718 single base substitution G T intron_variant MELA-AU 6 79684279 79684279 single base substitution C A intron_variant MELA-AU 6 79687905 79687905 single base substitution G A intron_variant MELA-AU 6 79688316 79688317 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 6 79688316 79688317 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant G961N 2881GG>AA MELA-AU 6 79688708 79688708 single base substitution G A intron_variant MELA-AU 6 79689189 79689189 single base substitution A G intron_variant MELA-AU 6 79690604 79690604 single base substitution G A intron_variant MELA-AU 6 79691750 79691750 single base substitution G A intron_variant MELA-AU 6 79692851 79692851 single base substitution G A intron_variant MELA-AU 6 79692851 79692851 single base substitution G A upstream_gene_variant MELA-AU 6 79692902 79692902 single base substitution G A intron_variant MELA-AU 6 79692902 79692902 single base substitution G A upstream_gene_variant MELA-AU 6 79693170 79693170 single base substitution G A intron_variant MELA-AU 6 79693170 79693170 single base substitution G A upstream_gene_variant MELA-AU 6 79693245 79693245 single base substitution G A intron_variant MELA-AU 6 79693245 79693245 single base substitution G A upstream_gene_variant MELA-AU 6 79693689 79693689 single base substitution A G intron_variant MELA-AU 6 79693689 79693689 single base substitution A G upstream_gene_variant MELA-AU 6 79693982 79693982 single base substitution G A intron_variant MELA-AU 6 79693982 79693982 single base substitution G A upstream_gene_variant MELA-AU 6 79694698 79694698 single base substitution T A intron_variant MELA-AU 6 79694698 79694698 single base substitution T A upstream_gene_variant MELA-AU 6 79695020 79695020 single base substitution T A intron_variant MELA-AU 6 79695020 79695020 single base substitution T A upstream_gene_variant MELA-AU 6 79695900 79695900 single base substitution A T intron_variant MELA-AU 6 79695900 79695900 single base substitution A T upstream_gene_variant MELA-AU 6 79696502 79696502 single base substitution G A intron_variant MELA-AU 6 79696502 79696502 single base substitution G A upstream_gene_variant MELA-AU 6 79696831 79696831 single base substitution T C intron_variant MELA-AU 6 79696831 79696831 single base substitution T C upstream_gene_variant MELA-AU 6 79696897 79696897 single base substitution C T intron_variant MELA-AU 6 79696897 79696897 single base substitution C T upstream_gene_variant MELA-AU 6 79698347 79698347 single base substitution G A intron_variant MELA-AU 6 79699236 79699236 single base substitution G A intron_variant MELA-AU 6 79699560 79699560 single base substitution T C intron_variant MELA-AU 6 79699616 79699616 single base substitution G C intron_variant MELA-AU 6 79699733 79699733 single base substitution G A intron_variant MELA-AU 6 79699875 79699875 single base substitution G A intron_variant MELA-AU 6 79699887 79699887 single base substitution G A intron_variant MELA-AU 6 79699978 79699978 single base substitution G A intron_variant MELA-AU 6 79700060 79700060 single base substitution G A intron_variant MELA-AU 6 79700161 79700161 single base substitution G A intron_variant MELA-AU 6 79700169 79700169 single base substitution G C intron_variant MELA-AU 6 79700825 79700825 single base substitution G A intron_variant MELA-AU 6 79700831 79700831 single base substitution G A intron_variant MELA-AU 6 79701269 79701269 single base substitution G A intron_variant MELA-AU 6 79701277 79701277 single base substitution G A intron_variant MELA-AU 6 79701365 79701365 single base substitution G C intron_variant MELA-AU 6 79701378 79701378 single base substitution G T intron_variant MELA-AU 6 79701740 79701740 single base substitution A G intron_variant MELA-AU 6 79701957 79701957 single base substitution G A intron_variant MELA-AU 6 79702698 79702698 single base substitution G A intron_variant MELA-AU 6 79702983 79702983 single base substitution G C intron_variant MELA-AU 6 79703002 79703002 single base substitution G A intron_variant MELA-AU 6 79703043 79703043 single base substitution G C intron_variant MELA-AU 6 79703928 79703928 single base substitution G C intron_variant MELA-AU 6 79704152 79704152 single base substitution G A intron_variant MELA-AU 6 79704368 79704368 single base substitution G C intron_variant MELA-AU 6 79705383 79705383 single base substitution C T intron_variant MELA-AU 6 79705567 79705567 single base substitution G C intron_variant MELA-AU 6 79706475 79706475 single base substitution C G intron_variant MELA-AU 6 79706851 79706851 single base substitution G C intron_variant MELA-AU 6 79707321 79707321 single base substitution G A splice_region_variant MELA-AU 6 79707449 79707449 single base substitution G A intron_variant MELA-AU 6 79707510 79707510 single base substitution G C intron_variant MELA-AU 6 79707552 79707552 single base substitution G A intron_variant MELA-AU 6 79707751 79707751 single base substitution G A intron_variant MELA-AU 6 79707754 79707754 single base substitution G A intron_variant MELA-AU 6 79707772 79707772 single base substitution C T intron_variant MELA-AU 6 79708587 79708587 single base substitution A G intron_variant MELA-AU 6 79708838 79708838 single base substitution T C intron_variant MELA-AU 6 79710640 79710640 single base substitution G A intron_variant MELA-AU 6 79711372 79711372 single base substitution G A intron_variant MELA-AU 6 79711476 79711476 single base substitution C T intron_variant MELA-AU 6 79711705 79711705 single base substitution G C missense_variant P597R 1790C>G MELA-AU 6 79711794 79711794 single base substitution A G synonymous_variant R567R 1701T>C MELA-AU 6 79712354 79712354 single base substitution G A intron_variant MELA-AU 6 79713475 79713475 single base substitution C G missense_variant G542A 1625G>C MELA-AU 6 79713601 79713601 single base substitution G C intron_variant MELA-AU 6 79715286 79715286 single base substitution G A intron_variant MELA-AU 6 79715841 79715841 single base substitution G A intron_variant MELA-AU 6 79716324 79716324 single base substitution A T intron_variant MELA-AU 6 79716717 79716717 single base substitution G A intron_variant MELA-AU 6 79716866 79716866 single base substitution G A intron_variant MELA-AU 6 79717560 79717560 single base substitution G A intron_variant MELA-AU 6 79717615 79717615 single base substitution G A intron_variant MELA-AU 6 79717724 79717724 single base substitution G A intron_variant MELA-AU 6 79717802 79717802 single base substitution G A intron_variant MELA-AU 6 79719819 79719819 single base substitution G A intron_variant MELA-AU 6 79719834 79719834 single base substitution G A intron_variant MELA-AU 6 79721403 79721403 single base substitution T C intron_variant MELA-AU 6 79722451 79722451 single base substitution G A intron_variant MELA-AU 6 79722821 79722821 single base substitution A C intron_variant MELA-AU 6 79724155 79724155 single base substitution G A intron_variant MELA-AU 6 79724930 79724930 single base substitution G A missense_variant H465Y 1393C>T MELA-AU 6 79726314 79726314 single base substitution A T missense_variant F394L 1182T>A MELA-AU 6 79726619 79726620 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 79726631 79726631 single base substitution G A intron_variant MELA-AU 6 79726717 79726717 single base substitution G A intron_variant MELA-AU 6 79727141 79727141 single base substitution A G intron_variant MELA-AU 6 79728040 79728040 single base substitution G C intron_variant MELA-AU 6 79728150 79728150 single base substitution G A intron_variant MELA-AU 6 79728916 79728916 single base substitution G A intron_variant MELA-AU 6 79729195 79729195 single base substitution G T intron_variant MELA-AU 6 79729388 79729388 single base substitution G A intron_variant MELA-AU 6 79730789 79730789 single base substitution T C intron_variant MELA-AU 6 79731823 79731823 single base substitution G A intron_variant MELA-AU 6 79732057 79732057 single base substitution T C intron_variant MELA-AU 6 79732120 79732120 single base substitution G A intron_variant MELA-AU 6 79734379 79734379 single base substitution G A intron_variant MELA-AU 6 79734419 79734419 single base substitution G A intron_variant MELA-AU 6 79735112 79735112 single base substitution G A intron_variant MELA-AU 6 79735277 79735277 single base substitution A G synonymous_variant T294T 882T>C MELA-AU 6 79735498 79735498 single base substitution G A intron_variant MELA-AU 6 79736536 79736536 single base substitution G A intron_variant MELA-AU 6 79736771 79736771 single base substitution G A intron_variant MELA-AU 6 79736839 79736840 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 79739571 79739571 single base substitution G A intron_variant MELA-AU 6 79739747 79739747 single base substitution G A intron_variant MELA-AU 6 79740499 79740499 single base substitution G A intron_variant MELA-AU 6 79742264 79742264 single base substitution G A intron_variant MELA-AU 6 79742940 79742940 single base substitution G A intron_variant MELA-AU 6 79743364 79743364 single base substitution G A intron_variant MELA-AU 6 79746461 79746461 single base substitution A G intron_variant MELA-AU 6 79748853 79748853 single base substitution G A intron_variant MELA-AU 6 79748873 79748873 single base substitution C T intron_variant MELA-AU 6 79749250 79749250 single base substitution T A intron_variant MELA-AU 6 79749415 79749415 single base substitution G A intron_variant MELA-AU 6 79750424 79750433 deletion of <=200bp CACTTGAAGT - intron_variant MELA-AU 6 79750469 79750469 single base substitution T C intron_variant MELA-AU 6 79751080 79751080 single base substitution G T intron_variant MELA-AU 6 79751222 79751222 single base substitution G A intron_variant MELA-AU 6 79751543 79751543 single base substitution G A intron_variant MELA-AU 6 79751680 79751680 single base substitution C T intron_variant MELA-AU 6 79751886 79751886 single base substitution G A intron_variant MELA-AU 6 79751991 79751991 single base substitution A G intron_variant MELA-AU 6 79752120 79752120 single base substitution G A intron_variant MELA-AU 6 79752690 79752691 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant G157K 469GG>AA MELA-AU 6 79753704 79753704 single base substitution C T intron_variant MELA-AU 6 79754245 79754245 single base substitution G A intron_variant MELA-AU 6 79754966 79754966 single base substitution T C intron_variant MELA-AU 6 79756486 79756486 single base substitution G A intron_variant MELA-AU 6 79756568 79756568 single base substitution G A intron_variant MELA-AU 6 79756610 79756610 single base substitution G A intron_variant MELA-AU 6 79757055 79757055 single base substitution C T intron_variant MELA-AU 6 79757462 79757462 single base substitution C A intron_variant MELA-AU 6 79758874 79758875 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 79758959 79758959 single base substitution A G intron_variant MELA-AU 6 79759033 79759033 single base substitution C A intron_variant MELA-AU 6 79759305 79759305 single base substitution G A intron_variant MELA-AU 6 79760762 79760762 single base substitution G A intron_variant MELA-AU 6 79761157 79761157 single base substitution A G intron_variant MELA-AU 6 79761294 79761294 single base substitution T C intron_variant MELA-AU 6 79761623 79761623 single base substitution T A intron_variant MELA-AU 6 79761694 79761694 single base substitution G A intron_variant MELA-AU 6 79761958 79761958 single base substitution G A intron_variant MELA-AU 6 79762173 79762174 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 6 79762310 79762310 single base substitution G A intron_variant MELA-AU 6 79764673 79764673 single base substitution T A intron_variant MELA-AU 6 79765412 79765412 single base substitution C G intron_variant MELA-AU 6 79765477 79765477 single base substitution G A intron_variant MELA-AU 6 79765852 79765852 single base substitution A G intron_variant MELA-AU 6 79766396 79766396 single base substitution G T intron_variant MELA-AU 6 79767732 79767732 single base substitution A G intron_variant MELA-AU 6 79769708 79769708 single base substitution A T intron_variant MELA-AU 6 79769816 79769816 single base substitution A T intron_variant MELA-AU 6 79770072 79770072 single base substitution C T intron_variant MELA-AU 6 79770235 79770235 single base substitution T C synonymous_variant P133P 399A>G MELA-AU 6 79770483 79770483 single base substitution C T missense_variant R81Q 242G>A MELA-AU 6 79770716 79770716 single base substitution G A intron_variant MELA-AU 6 79771371 79771371 single base substitution C T intron_variant MELA-AU 6 79772023 79772023 single base substitution G A intron_variant MELA-AU 6 79773756 79773756 single base substitution G A intron_variant MELA-AU 6 79774386 79774386 single base substitution A G intron_variant MELA-AU 6 79776634 79776634 single base substitution G A intron_variant MELA-AU 6 79777296 79777296 single base substitution A G intron_variant MELA-AU 6 79778212 79778212 single base substitution G A intron_variant MELA-AU 6 79778979 79778979 single base substitution A G intron_variant MELA-AU 6 79779023 79779023 single base substitution T C intron_variant MELA-AU 6 79781426 79781426 single base substitution G A intron_variant MELA-AU 6 79781730 79781730 single base substitution C T intron_variant MELA-AU 6 79782114 79782114 single base substitution A C intron_variant MELA-AU 6 79782867 79782867 deletion of <=200bp A - intron_variant MELA-AU 6 79783478 79783478 single base substitution T G intron_variant MELA-AU 6 79783949 79783949 single base substitution C G intron_variant MELA-AU 6 79784477 79784488 deletion of <=200bp CTTTTAAAACTG - intron_variant MELA-AU 6 79788147 79788148 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 6 79788892 79788892 single base substitution C T upstream_gene_variant MELA-AU 6 79789714 79789714 single base substitution C T upstream_gene_variant MELA-AU 6 79790573 79790573 single base substitution C T upstream_gene_variant MELA-AU 6 79790966 79790967 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 6 79791135 79791135 insertion of <=200bp - A upstream_gene_variant MELA-AU 6 79791437 79791437 single base substitution C T upstream_gene_variant MELA-AU 6 79791538 79791538 single base substitution C T upstream_gene_variant MELA-AU 6 79791973 79791973 single base substitution G A upstream_gene_variant MELA-AU 6 79792152 79792152 single base substitution C T upstream_gene_variant MELA-AU 6 79792292 79792292 single base substitution G A upstream_gene_variant MELA-AU 6 79792372 79792372 single base substitution C T upstream_gene_variant MELA-AU 6 79792607 79792607 single base substitution G A upstream_gene_variant MELA-AU 6 79792701 79792701 single base substitution T A upstream_gene_variant MELA-AU 6 79792742 79792742 single base substitution T G upstream_gene_variant MELA-AU 6 79792936 79792936 single base substitution C T upstream_gene_variant ORCA-IN 6 79664632 79664632 single base substitution T C exon_variant ORCA-IN 6 79664632 79664632 single base substitution T C missense_variant I1318V 3952A>G ORCA-IN 6 79668221 79668221 single base substitution G A exon_variant ORCA-IN 6 79668221 79668221 single base substitution G A synonymous_variant F1251F 3753C>T ORCA-IN 6 79673326 79673326 single base substitution A T intron_variant ORCA-IN 6 79680572 79680572 single base substitution C T exon_variant ORCA-IN 6 79680572 79680572 single base substitution C T missense_variant V975I 2923G>A ORCA-IN 6 79700618 79700618 single base substitution A T synonymous_variant V762V 2286T>A ORCA-IN 6 79734337 79734337 single base substitution C T intron_variant ORCA-IN 6 79737773 79737773 single base substitution G C intron_variant ORCA-IN 6 79760924 79760924 single base substitution C A intron_variant ORCA-IN 6 79769696 79769696 single base substitution G A intron_variant ORCA-IN 6 79770258 79770258 single base substitution C A missense_variant A126S 376G>T OV-AU 6 79642743 79642743 single base substitution G T downstream_gene_variant OV-AU 6 79643751 79643751 single base substitution A G downstream_gene_variant OV-AU 6 79645609 79645609 single base substitution T C 3_prime_UTR_variant OV-AU 6 79645609 79645609 single base substitution T C downstream_gene_variant OV-AU 6 79656010 79656010 single base substitution A G intron_variant OV-AU 6 79657941 79657941 single base substitution A T intron_variant OV-AU 6 79664252 79664252 single base substitution A T intron_variant OV-AU 6 79669219 79669219 single base substitution G A intron_variant OV-AU 6 79675334 79675334 single base substitution A T intron_variant OV-AU 6 79675338 79675338 single base substitution G T intron_variant OV-AU 6 79682091 79682091 single base substitution C A intron_variant OV-AU 6 79683691 79683691 single base substitution G C intron_variant OV-AU 6 79689305 79689305 single base substitution C T intron_variant OV-AU 6 79691093 79691093 single base substitution C T intron_variant OV-AU 6 79692950 79692950 single base substitution T A intron_variant OV-AU 6 79692950 79692950 single base substitution T A upstream_gene_variant OV-AU 6 79720904 79720904 single base substitution G C intron_variant OV-AU 6 79734622 79734622 single base substitution T G intron_variant OV-AU 6 79739534 79739534 single base substitution G A intron_variant OV-AU 6 79743139 79743139 single base substitution G A intron_variant OV-AU 6 79746011 79746011 single base substitution A G intron_variant OV-AU 6 79746446 79746446 single base substitution G C intron_variant OV-AU 6 79756684 79756684 single base substitution G C intron_variant OV-AU 6 79757444 79757444 single base substitution T C intron_variant OV-AU 6 79761840 79761840 single base substitution G C intron_variant OV-AU 6 79766281 79766281 single base substitution G A intron_variant OV-AU 6 79766735 79766735 single base substitution G A intron_variant OV-AU 6 79769128 79769128 single base substitution A G intron_variant OV-AU 6 79772667 79772667 single base substitution C A intron_variant OV-AU 6 79776268 79776268 single base substitution G A intron_variant OV-AU 6 79779460 79779460 single base substitution C A intron_variant OV-AU 6 79785001 79785001 single base substitution C A intron_variant OV-AU 6 79787987 79787987 single base substitution T G upstream_gene_variant OV-AU 6 79792281 79792281 single base substitution A C upstream_gene_variant PACA-AU 6 79665211 79665211 insertion of <=200bp - A intron_variant PACA-AU 6 79668989 79668989 single base substitution A G intron_variant PACA-AU 6 79671863 79671865 deletion of <=200bp TAT - intron_variant PACA-AU 6 79672627 79672627 single base substitution A C intron_variant PACA-AU 6 79672660 79672660 single base substitution T A intron_variant PACA-AU 6 79675510 79675510 single base substitution A G intron_variant PACA-AU 6 79676307 79676307 single base substitution A C intron_variant PACA-AU 6 79680762 79680762 single base substitution C T intron_variant PACA-AU 6 79681241 79681241 single base substitution G A intron_variant PACA-AU 6 79688266 79688268 deletion of <=200bp AAC - intron_variant PACA-AU 6 79689242 79689242 single base substitution G A intron_variant PACA-AU 6 79692529 79692529 single base substitution C G intron_variant PACA-AU 6 79702930 79702930 single base substitution A G intron_variant PACA-AU 6 79713953 79713953 single base substitution T C intron_variant PACA-AU 6 79715257 79715257 single base substitution G T intron_variant PACA-AU 6 79723939 79723939 single base substitution G A intron_variant PACA-AU 6 79724895 79724895 single base substitution C T synonymous_variant P476P 1428G>A PACA-AU 6 79727378 79727378 single base substitution C T intron_variant PACA-AU 6 79729838 79729838 single base substitution T G intron_variant PACA-AU 6 79733632 79733632 single base substitution G T intron_variant PACA-AU 6 79733822 79733822 single base substitution A G intron_variant PACA-AU 6 79734560 79734560 single base substitution A G intron_variant PACA-AU 6 79737229 79737229 single base substitution G A intron_variant PACA-AU 6 79741468 79741468 single base substitution A C intron_variant PACA-AU 6 79741474 79741474 single base substitution A G intron_variant PACA-AU 6 79751840 79751842 deletion of <=200bp ATC - intron_variant PACA-AU 6 79752036 79752049 deletion of <=200bp AAGAATGAACTGTT - intron_variant PACA-AU 6 79759649 79759649 single base substitution T C intron_variant PACA-AU 6 79764673 79764673 single base substitution T A intron_variant PACA-AU 6 79771709 79771709 single base substitution A C intron_variant PACA-AU 6 79772995 79772995 single base substitution A G intron_variant PACA-AU 6 79780687 79780687 single base substitution A C intron_variant PACA-AU 6 79789601 79789601 single base substitution T G upstream_gene_variant PACA-CA 6 79644186 79644186 single base substitution A C downstream_gene_variant PACA-CA 6 79644801 79644801 single base substitution T C downstream_gene_variant PACA-CA 6 79645434 79645434 single base substitution C T downstream_gene_variant PACA-CA 6 79648062 79648062 single base substitution G C 3_prime_UTR_variant PACA-CA 6 79648062 79648062 single base substitution G C downstream_gene_variant PACA-CA 6 79650877 79650877 single base substitution G A exon_variant PACA-CA 6 79650877 79650877 single base substitution G A stop_gained Q1667* 4999C>T PACA-CA 6 79654795 79654795 single base substitution A C intron_variant PACA-CA 6 79658176 79658176 single base substitution G A intron_variant PACA-CA 6 79670815 79670815 single base substitution T A intron_variant PACA-CA 6 79672347 79672347 single base substitution G A intron_variant PACA-CA 6 79673787 79673787 single base substitution C T intron_variant PACA-CA 6 79674405 79674405 single base substitution T A intron_variant PACA-CA 6 79674406 79674406 single base substitution C G intron_variant PACA-CA 6 79675549 79675549 single base substitution T G intron_variant PACA-CA 6 79680999 79680999 single base substitution T C intron_variant PACA-CA 6 79694133 79694133 single base substitution G T intron_variant PACA-CA 6 79694133 79694133 single base substitution G T upstream_gene_variant PACA-CA 6 79695223 79695223 single base substitution A G intron_variant PACA-CA 6 79695223 79695223 single base substitution A G upstream_gene_variant PACA-CA 6 79695417 79695417 single base substitution G T intron_variant PACA-CA 6 79695417 79695417 single base substitution G T upstream_gene_variant PACA-CA 6 79697960 79697960 single base substitution G A missense_variant S809L 2426C>T PACA-CA 6 79700897 79700897 single base substitution G T intron_variant PACA-CA 6 79701920 79701920 single base substitution C T intron_variant PACA-CA 6 79703844 79703844 single base substitution C T intron_variant PACA-CA 6 79709730 79709730 single base substitution A G intron_variant PACA-CA 6 79711300 79711300 single base substitution A C intron_variant PACA-CA 6 79718054 79718054 single base substitution G A intron_variant PACA-CA 6 79722716 79722716 single base substitution A G intron_variant PACA-CA 6 79723660 79723660 deletion of <=200bp T - intron_variant PACA-CA 6 79725685 79725685 single base substitution T C intron_variant PACA-CA 6 79726271 79726271 single base substitution G C missense_variant R409G 1225C>G PACA-CA 6 79728592 79728592 single base substitution A T intron_variant PACA-CA 6 79730467 79730467 single base substitution G T intron_variant PACA-CA 6 79734163 79734163 single base substitution C A intron_variant PACA-CA 6 79734724 79734724 single base substitution A G intron_variant PACA-CA 6 79735479 79735479 single base substitution T C intron_variant PACA-CA 6 79740654 79740654 single base substitution T G intron_variant PACA-CA 6 79745223 79745223 single base substitution G T intron_variant PACA-CA 6 79745806 79745806 single base substitution A G intron_variant PACA-CA 6 79747444 79747444 single base substitution A G intron_variant PACA-CA 6 79750374 79750374 single base substitution C T intron_variant PACA-CA 6 79751149 79751149 single base substitution C T intron_variant PACA-CA 6 79752943 79752943 single base substitution G T intron_variant PACA-CA 6 79755392 79755392 single base substitution G C intron_variant PACA-CA 6 79761626 79761626 single base substitution T C intron_variant PACA-CA 6 79761637 79761637 insertion of <=200bp - T intron_variant PACA-CA 6 79763724 79763724 deletion of <=200bp T - intron_variant PACA-CA 6 79764296 79764296 single base substitution C A intron_variant PACA-CA 6 79768298 79768299 deletion of <=200bp GC - intron_variant PACA-CA 6 79777947 79777947 single base substitution A G intron_variant PACA-CA 6 79785853 79785853 single base substitution C G intron_variant PACA-CA 6 79789239 79789239 single base substitution T C upstream_gene_variant PACA-CA 6 79791049 79791049 single base substitution C T upstream_gene_variant PACA-CA 6 79791083 79791083 single base substitution A C upstream_gene_variant PACA-CA 6 79791503 79791503 single base substitution A G upstream_gene_variant PACA-CA 6 79792423 79792423 single base substitution A G upstream_gene_variant PAEN-AU 6 79644345 79644345 single base substitution T A downstream_gene_variant PAEN-AU 6 79707436 79707436 single base substitution A T intron_variant PAEN-AU 6 79716448 79716448 single base substitution G A intron_variant PAEN-AU 6 79733102 79733102 single base substitution C A intron_variant PBCA-DE 6 79656601 79656601 deletion of <=200bp A - intron_variant PBCA-DE 6 79665714 79665717 deletion of <=200bp TCTT - exon_variant PBCA-DE 6 79665714 79665717 deletion of <=200bp TCTT - intron_variant PBCA-DE 6 79670184 79670184 single base substitution C T intron_variant PBCA-DE 6 79675879 79675879 single base substitution G A intron_variant PBCA-DE 6 79678341 79678341 single base substitution T C intron_variant PBCA-DE 6 79684816 79684819 deletion of <=200bp ATGA - intron_variant PBCA-DE 6 79695944 79695944 single base substitution G T intron_variant PBCA-DE 6 79695944 79695944 single base substitution G T upstream_gene_variant PBCA-DE 6 79701713 79701713 insertion of <=200bp - CT intron_variant PBCA-DE 6 79717471 79717471 single base substitution A T intron_variant PBCA-DE 6 79729990 79729990 single base substitution A G intron_variant PBCA-DE 6 79731021 79731021 single base substitution G A intron_variant PBCA-DE 6 79740429 79740429 single base substitution C T intron_variant PBCA-DE 6 79746960 79746960 single base substitution G A intron_variant PBCA-DE 6 79751202 79751202 insertion of <=200bp - TAACTT intron_variant PBCA-DE 6 79760231 79760231 single base substitution A G intron_variant PBCA-DE 6 79760377 79760377 insertion of <=200bp - A intron_variant PBCA-DE 6 79761099 79761099 insertion of <=200bp - A intron_variant PBCA-DE 6 79780688 79780688 insertion of <=200bp - C intron_variant PBCA-DE 6 79782897 79782897 single base substitution T C intron_variant PBCA-DE 6 79785305 79785305 single base substitution A C intron_variant PRAD-CA 6 79643109 79643109 single base substitution C T downstream_gene_variant PRAD-CA 6 79654814 79654814 single base substitution C T intron_variant PRAD-CA 6 79657391 79657391 single base substitution G A exon_variant PRAD-CA 6 79657391 79657391 single base substitution G A synonymous_variant V1385V 4155C>T PRAD-CA 6 79662145 79662145 single base substitution G A intron_variant PRAD-CA 6 79662158 79662158 single base substitution G A intron_variant PRAD-CA 6 79678211 79678211 single base substitution G A intron_variant PRAD-CA 6 79679577 79679577 single base substitution A G exon_variant PRAD-CA 6 79679577 79679577 single base substitution A G synonymous_variant D1060D 3180T>C PRAD-CA 6 79690290 79690290 single base substitution G A intron_variant PRAD-CA 6 79700980 79700980 single base substitution T C intron_variant PRAD-CA 6 79701972 79701972 single base substitution G A intron_variant PRAD-CA 6 79702521 79702521 single base substitution T C intron_variant PRAD-CA 6 79711379 79711379 single base substitution C A intron_variant PRAD-CA 6 79727006 79727006 single base substitution A G intron_variant PRAD-CA 6 79729887 79729887 single base substitution T A intron_variant PRAD-CA 6 79759133 79759133 single base substitution C A intron_variant PRAD-CA 6 79769056 79769056 single base substitution A T intron_variant PRAD-CA 6 79782209 79782209 single base substitution C T intron_variant PRAD-CA 6 79785607 79785607 single base substitution C T intron_variant PRAD-CA 6 79790982 79790982 single base substitution A G upstream_gene_variant PRAD-CA 6 79792554 79792554 single base substitution G T upstream_gene_variant PRAD-UK 6 79653249 79653249 single base substitution G T intron_variant PRAD-UK 6 79657269 79657269 single base substitution G A intron_variant PRAD-UK 6 79658734 79658734 single base substitution C G intron_variant PRAD-UK 6 79662769 79662769 single base substitution T A intron_variant PRAD-UK 6 79682324 79682324 single base substitution G C intron_variant PRAD-UK 6 79700275 79700275 single base substitution G C intron_variant PRAD-UK 6 79709747 79709747 single base substitution T C intron_variant PRAD-UK 6 79720943 79720943 single base substitution T G intron_variant PRAD-UK 6 79754329 79754329 single base substitution A G intron_variant PRAD-UK 6 79754676 79754676 insertion of <=200bp - A intron_variant PRAD-UK 6 79778753 79778753 single base substitution G A intron_variant PRAD-US 6 79692791 79692791 single base substitution T A missense_variant I861F 2581A>T PRAD-US 6 79692791 79692791 single base substitution T A upstream_gene_variant PRAD-US 6 79770385 79770385 single base substitution T A missense_variant S114C 340A>T READ-US 6 79650763 79650763 single base substitution A C exon_variant READ-US 6 79650763 79650763 single base substitution A C missense_variant L1705V 5113T>G READ-US 6 79657465 79657465 single base substitution T C exon_variant READ-US 6 79657465 79657465 single base substitution T C missense_variant M1361V 4081A>G READ-US 6 79664635 79664635 single base substitution C T exon_variant READ-US 6 79664635 79664635 single base substitution C T missense_variant D1317N 3949G>A READ-US 6 79664656 79664656 single base substitution G A exon_variant READ-US 6 79664656 79664656 single base substitution G A missense_variant R1310C 3928C>T READ-US 6 79668267 79668267 single base substitution C T exon_variant READ-US 6 79668267 79668267 single base substitution C T missense_variant R1236Q 3707G>A READ-US 6 79692787 79692787 single base substitution T C missense_variant N862S 2585A>G READ-US 6 79692787 79692787 single base substitution T C upstream_gene_variant READ-US 6 79724815 79724815 single base substitution C T missense_variant R503Q 1508G>A READ-US 6 79726270 79726270 single base substitution C T missense_variant R409H 1226G>A READ-US 6 79726309 79726309 single base substitution C T missense_variant R396Q 1187G>A READ-US 6 79726343 79726343 single base substitution G A missense_variant R385C 1153C>T RECA-EU 6 79648916 79648916 single base substitution C A 3_prime_UTR_variant RECA-EU 6 79648916 79648916 single base substitution C A downstream_gene_variant RECA-EU 6 79650814 79650814 single base substitution G C exon_variant RECA-EU 6 79650814 79650814 single base substitution G C missense_variant P1688A 5062C>G RECA-EU 6 79660575 79660575 single base substitution A G intron_variant RECA-EU 6 79672218 79672218 single base substitution G A intron_variant RECA-EU 6 79672219 79672219 single base substitution C A intron_variant RECA-EU 6 79673616 79673616 single base substitution C T intron_variant RECA-EU 6 79674684 79674684 single base substitution A G intron_variant RECA-EU 6 79701007 79701007 single base substitution A C intron_variant RECA-EU 6 79709732 79709732 single base substitution T C intron_variant RECA-EU 6 79710275 79710275 single base substitution A G intron_variant RECA-EU 6 79714829 79714829 single base substitution A T intron_variant RECA-EU 6 79727614 79727614 single base substitution G A intron_variant RECA-EU 6 79758128 79758128 single base substitution A T intron_variant RECA-EU 6 79766185 79766185 single base substitution A T intron_variant SKCA-BR 6 79642581 79642581 single base substitution T C downstream_gene_variant SKCA-BR 6 79654238 79654238 single base substitution G A intron_variant SKCA-BR 6 79656918 79656918 single base substitution C G intron_variant SKCA-BR 6 79669185 79669185 single base substitution C G intron_variant SKCA-BR 6 79674267 79674267 single base substitution T C intron_variant SKCA-BR 6 79675380 79675380 single base substitution A T intron_variant SKCA-BR 6 79675381 79675381 single base substitution C T intron_variant SKCA-BR 6 79679604 79679604 single base substitution G A exon_variant SKCA-BR 6 79679604 79679604 single base substitution G A synonymous_variant F1051F 3153C>T SKCA-BR 6 79681462 79681462 single base substitution C T intron_variant SKCA-BR 6 79681881 79681881 single base substitution T C intron_variant SKCA-BR 6 79681883 79681883 single base substitution C T intron_variant SKCA-BR 6 79681979 79681979 single base substitution G A intron_variant SKCA-BR 6 79681995 79681995 single base substitution C T intron_variant SKCA-BR 6 79686172 79686172 single base substitution A G intron_variant SKCA-BR 6 79688335 79688335 single base substitution G A exon_variant SKCA-BR 6 79688335 79688335 single base substitution G A missense_variant P955S 2863C>T SKCA-BR 6 79689361 79689361 single base substitution A T intron_variant SKCA-BR 6 79689828 79689828 single base substitution C A intron_variant SKCA-BR 6 79689852 79689852 single base substitution A C intron_variant SKCA-BR 6 79693272 79693272 single base substitution G A intron_variant SKCA-BR 6 79693272 79693272 single base substitution G A upstream_gene_variant SKCA-BR 6 79698634 79698634 single base substitution A C intron_variant SKCA-BR 6 79701570 79701571 deletion of <=200bp AT - intron_variant SKCA-BR 6 79701681 79701681 single base substitution C T intron_variant SKCA-BR 6 79705984 79705984 single base substitution G A intron_variant SKCA-BR 6 79706412 79706412 single base substitution G A intron_variant SKCA-BR 6 79707912 79707912 single base substitution G A intron_variant SKCA-BR 6 79715928 79715928 single base substitution A G intron_variant SKCA-BR 6 79727498 79727498 single base substitution G A intron_variant SKCA-BR 6 79755841 79755841 single base substitution A C intron_variant SKCA-BR 6 79755867 79755867 single base substitution T C intron_variant SKCA-BR 6 79757113 79757113 single base substitution A C intron_variant SKCA-BR 6 79758791 79758791 insertion of <=200bp - CT intron_variant SKCA-BR 6 79759465 79759466 deletion of <=200bp AT - intron_variant SKCA-BR 6 79759483 79759483 single base substitution G A intron_variant SKCA-BR 6 79761192 79761192 single base substitution A C intron_variant SKCA-BR 6 79766085 79766085 single base substitution T C intron_variant SKCA-BR 6 79771340 79771340 single base substitution G A intron_variant SKCA-BR 6 79773094 79773094 single base substitution T G intron_variant SKCA-BR 6 79775481 79775485 deletion of <=200bp CCACA - intron_variant SKCA-BR 6 79776627 79776627 single base substitution G A intron_variant SKCA-BR 6 79783036 79783041 deletion of <=200bp CGCCTA - intron_variant SKCA-BR 6 79783044 79783044 single base substitution A C intron_variant SKCA-BR 6 79785294 79785294 single base substitution A C intron_variant SKCA-BR 6 79786805 79786805 single base substitution T C intron_variant SKCA-BR 6 79786821 79786821 single base substitution T C intron_variant SKCA-BR 6 79787277 79787277 single base substitution T C intron_variant SKCA-BR 6 79787282 79787282 single base substitution T C intron_variant SKCA-BR 6 79788266 79788266 single base substitution A G upstream_gene_variant SKCA-BR 6 79789717 79789717 single base substitution G C upstream_gene_variant SKCA-BR 6 79789740 79789740 single base substitution G A upstream_gene_variant SKCA-BR 6 79790656 79790656 single base substitution A G upstream_gene_variant SKCA-BR 6 79791537 79791537 single base substitution C T upstream_gene_variant SKCM-US 6 79655836 79655836 deletion of <=200bp A - exon_variant SKCM-US 6 79655836 79655836 deletion of <=200bp A - frameshift_variant V1504 SKCM-US 6 79664553 79664553 single base substitution G A exon_variant SKCM-US 6 79664553 79664553 single base substitution G A missense_variant P1344L 4031C>T SKCM-US 6 79664602 79664602 single base substitution A G exon_variant SKCM-US 6 79664602 79664602 single base substitution A G synonymous_variant L1328L 3982T>C SKCM-US 6 79671440 79671440 single base substitution G A exon_variant SKCM-US 6 79671440 79671440 single base substitution G A missense_variant T1208I 3623C>T SKCM-US 6 79708059 79708059 insertion of <=200bp - A frameshift_variant L643L? SKCM-US 6 79725486 79725486 single base substitution C T missense_variant G417E 1250G>A SKCM-US 6 79787191 79787191 single base substitution C T missense_variant E55K 163G>A SKCM-US 6 79787588 79787588 single base substitution C T missense_variant C28Y 83G>A STAD-US 6 79655139 79655139 single base substitution C T exon_variant STAD-US 6 79655139 79655139 single base substitution C T missense_variant G1569D 4706G>A STAD-US 6 79655834 79655834 single base substitution C T exon_variant STAD-US 6 79655834 79655834 single base substitution C T missense_variant R1505Q 4514G>A STAD-US 6 79655835 79655835 single base substitution G C exon_variant STAD-US 6 79655835 79655835 single base substitution G C missense_variant R1505G 4513C>G STAD-US 6 79656535 79656535 single base substitution A C exon_variant STAD-US 6 79656535 79656535 single base substitution A C synonymous_variant V1421V 4263T>G STAD-US 6 79664656 79664656 single base substitution G A exon_variant STAD-US 6 79664656 79664656 single base substitution G A missense_variant R1310C 3928C>T STAD-US 6 79668246 79668246 single base substitution C T exon_variant STAD-US 6 79668246 79668246 single base substitution C T missense_variant S1243N 3728G>A STAD-US 6 79675723 79675723 single base substitution C T exon_variant STAD-US 6 79675723 79675723 single base substitution C T missense_variant E1086K 3256G>A STAD-US 6 79695140 79695140 single base substitution G A synonymous_variant G822G 2466C>T STAD-US 6 79695140 79695140 single base substitution G A upstream_gene_variant STAD-US 6 79700597 79700597 single base substitution G T synonymous_variant P769P 2307C>A STAD-US 6 79707231 79707231 single base substitution T A missense_variant M701L 2101A>T STAD-US 6 79708078 79708078 single base substitution T G missense_variant N637T 1910A>C STAD-US 6 79711671 79711671 single base substitution G A synonymous_variant G608G 1824C>T STAD-US 6 79724917 79724917 single base substitution A G missense_variant V469A 1406T>C STAD-US 6 79726328 79726328 single base substitution G A missense_variant R390C 1168C>T STAD-US 6 79726343 79726343 single base substitution G A missense_variant R385C 1153C>T STAD-US 6 79752650 79752650 single base substitution A G synonymous_variant Y170Y 510T>C STAD-US 6 79770253 79770253 single base substitution C T synonymous_variant A127A 381G>A THCA-SA 6 79647363 79647363 single base substitution G A 3_prime_UTR_variant THCA-SA 6 79647363 79647363 single base substitution G A downstream_gene_variant THCA-US 6 79707237 79707237 single base substitution G A missense_variant R699W 2095C>T UCEC-US 6 79650576 79650576 single base substitution C T exon_variant UCEC-US 6 79650576 79650576 single base substitution C T missense_variant R1767K 5300G>A UCEC-US 6 79650691 79650691 single base substitution G T exon_variant UCEC-US 6 79650691 79650691 single base substitution G T missense_variant L1729I 5185C>A UCEC-US 6 79650975 79650975 single base substitution A C exon_variant UCEC-US 6 79650975 79650975 single base substitution A C missense_variant L1634R 4901T>G UCEC-US 6 79651023 79651023 single base substitution A G exon_variant UCEC-US 6 79651023 79651023 single base substitution A G missense_variant V1618A 4853T>C UCEC-US 6 79655035 79655035 single base substitution A G exon_variant UCEC-US 6 79655035 79655035 single base substitution A G missense_variant S1604P 4810T>C UCEC-US 6 79655055 79655055 single base substitution G A exon_variant UCEC-US 6 79655055 79655055 single base substitution G A missense_variant A1597V 4790C>T UCEC-US 6 79655764 79655764 single base substitution C A exon_variant UCEC-US 6 79655764 79655764 single base substitution C A missense_variant K1528N 4584G>T UCEC-US 6 79655853 79655853 single base substitution C A exon_variant UCEC-US 6 79655853 79655853 single base substitution C A stop_gained E1499* 4495G>T UCEC-US 6 79655900 79655900 single base substitution C T exon_variant UCEC-US 6 79655900 79655900 single base substitution C T missense_variant R1483Q 4448G>A UCEC-US 6 79655966 79655966 single base substitution T G exon_variant UCEC-US 6 79655966 79655966 single base substitution T G missense_variant K1461T 4382A>C UCEC-US 6 79664566 79664566 single base substitution G A exon_variant UCEC-US 6 79664566 79664566 single base substitution G A missense_variant P1340S 4018C>T UCEC-US 6 79664991 79664991 single base substitution C A exon_variant UCEC-US 6 79664991 79664991 single base substitution C A missense_variant E1287D 3861G>T UCEC-US 6 79665344 79665344 single base substitution A C exon_variant UCEC-US 6 79665344 79665344 single base substitution A C missense_variant L1280V 3838T>G UCEC-US 6 79668220 79668220 single base substitution C T exon_variant UCEC-US 6 79668220 79668220 single base substitution C T missense_variant V1252M 3754G>A UCEC-US 6 79668221 79668221 single base substitution G A exon_variant UCEC-US 6 79668221 79668221 single base substitution G A synonymous_variant F1251F 3753C>T UCEC-US 6 79668241 79668241 single base substitution T C exon_variant UCEC-US 6 79668241 79668241 single base substitution T C missense_variant I1245V 3733A>G UCEC-US 6 79668288 79668288 single base substitution C T exon_variant UCEC-US 6 79668288 79668288 single base substitution C T missense_variant R1229Q 3686G>A UCEC-US 6 79672846 79672846 single base substitution A C exon_variant UCEC-US 6 79672846 79672846 single base substitution A C missense_variant I1168S 3503T>G UCEC-US 6 79672943 79672943 single base substitution T C exon_variant UCEC-US 6 79672943 79672943 single base substitution T C missense_variant S1136G 3406A>G UCEC-US 6 79675690 79675690 single base substitution C G exon_variant UCEC-US 6 79675690 79675690 single base substitution C G missense_variant D1097H 3289G>C UCEC-US 6 79679564 79679564 single base substitution G A exon_variant UCEC-US 6 79679564 79679564 single base substitution G A stop_gained R1065* 3193C>T UCEC-US 6 79680569 79680569 single base substitution C T exon_variant UCEC-US 6 79680569 79680569 single base substitution C T missense_variant E976K 2926G>A UCEC-US 6 79707306 79707306 single base substitution T G missense_variant S676R 2026A>C UCEC-US 6 79708099 79708099 single base substitution T G missense_variant Q630P 1889A>C UCEC-US 6 79713458 79713458 single base substitution T C missense_variant K548E 1642A>G UCEC-US 6 79725406 79725406 single base substitution T G missense_variant N444H 1330A>C UCEC-US 6 79726309 79726309 single base substitution C T missense_variant R396Q 1187G>A UCEC-US 6 79727063 79727063 single base substitution C A missense_variant R379M 1136G>T UCEC-US 6 79727227 79727227 single base substitution C A missense_variant E356D 1068G>T UCEC-US 6 79735285 79735285 single base substitution C A missense_variant D292Y 874G>T UCEC-US 6 79735659 79735659 single base substitution C T splice_donor_variant UCEC-US 6 79735718 79735718 single base substitution C T missense_variant R255Q 764G>A UCEC-US 6 79770485 79770485 single base substitution A G synonymous_variant H80H 240T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCC2998 COSM1672580 c.1378C>A p.H460N Substitution - Missense 6:79015641-79015641 - CN-AML-NR-08-Dx COSM3762194 c.3278T>C p.L1093P Substitution - Missense 6:78965984-78965984 - TCGA-B0-5707-01 COSM484379 c.4792T>C p.S1598P Substitution - Missense 6:78945336-78945336 - TCGA-E2-A56Z-01 COSM5835268 c.2377delC p.Q793fs*20 Deletion - Frameshift 6:78988292-78988292 - TCGA-EI-6917-01 COSM3430898 c.3949G>A p.D1317N Substitution - Missense 6:78954918-78954918 - tumor_4139696 COSM3358051 c.311G>T p.G104V Substitution - Missense 6:79060697-79060697 - 304_T COSM3949487 c.5147C>T p.P1716L Substitution - Missense 6:78941012-78941012 - CN-AML-NR-15-Dx COSM5427326 c.3468G>A p.W1156* Substitution - Nonsense 6:78963164-78963164 - sysucc-274T COSM5476711 c.1169G>A p.R390H Substitution - Missense 6:79016610-79016610 - PCSI_0547_Pa_P_526 COSM5032130 c.1225C>G p.R409G Substitution - Missense 6:79016554-79016554 - LC_C9 COSM1187092 c.1712A>G p.N571S Substitution - Missense 6:79002066-79002066 - 587342 COSM1220395 c.2537G>T p.S846I Substitution - Missense 6:78985352-78985352 - LS411 COSM3175988 c.2306C>A p.P769H Substitution - Missense 6:78990881-78990881 - TCGA-A8-A09Z-01 COSM5202444 c.2656_2658delGAA p.E886delE Deletion - In frame 6:78982997-78982999 - CRC-8 COSM304495 c.2897A>G p.Y966C Substitution - Missense 6:78970881-78970881 - TCGA-AX-A05Z-01 COSM1081854 c.3733A>G p.I1245V Substitution - Missense 6:78958524-78958524 - PD4194a COSM219580 c.1285A>G p.M429V Substitution - Missense 6:79015734-79015734 - 388 COSM98117 c.3301C>G p.Q1101E Substitution - Missense 6:78965961-78965961 - TCGA-CG-5733-01 COSM3176019 c.381G>A p.A127A Substitution - coding silent 6:79060536-79060536 - MO_1232 COSM5564627 c.4910G>C p.R1637T Substitution - Missense 6:78941249-78941249 - LUAD-E00443 COSM364043 c.4360G>T p.A1454S Substitution - Missense 6:78946721-78946721 - TCGA-DC-6158-01 COSM1568251 c.4081A>G p.M1361V Substitution - Missense 6:78947748-78947748 - TCGA-AD-5900-01 COSM1446061 c.329G>A p.R110H Substitution - Missense 6:79060679-79060679 - TCGA-D1-A15X-01 COSM1081842 c.4853T>C p.V1618A Substitution - Missense 6:78941306-78941306 - TCGA-Q1-A6DT-01 COSM4850889 c.4427C>T p.S1476F Substitution - Missense 6:78946204-78946204 - S00946 COSM196940 c.2113G>A p.A705T Substitution - Missense 6:78997502-78997502 - CSCC-56-T COSM4571616 c.5020T>A p.L1674I Substitution - Missense 6:78941139-78941139 - RMS85_ COSM4988896 c.5284T>C p.S1762P Substitution - Missense 6:78940875-78940875 - TCGA-AA-A00N-01 COSM276733 c.1036C>T p.R346W Substitution - Missense 6:79017542-79017542 - sysucc-657T COSM4880462 c.3180T>C p.D1060D Substitution - coding silent 6:78969860-78969860 - SJHGG034_D COSM4970520 c.5227C>T p.R1743* Substitution - Nonsense 6:78940932-78940932 - 229 COSM4426335 c.5052T>C p.D1684D Substitution - coding silent 6:78941107-78941107 - PT37 COSM5919067 c.1083G>C p.L361F Substitution - Missense 6:79017495-79017495 - NPC15F COSM3175995 c.1934G>A p.S645N Substitution - Missense 6:78998337-78998337 - TCGA-FW-A3R5-06 COSM3922200 c.1250G>A p.G417E Substitution - Missense 6:79015769-79015769 - TCGA-AP-A0LM-01 COSM1081851 c.3861G>T p.E1287D Substitution - Missense 6:78955274-78955274 - WSU-HN12 COSM4601317 c.4061G>C p.R1354T Substitution - Missense 6:78947768-78947768 - TCGA-FS-A4F5-06 COSM39331 c.4031C>T p.P1344L Substitution - Missense 6:78954836-78954836 - TCGA-D1-A16N-01 COSM1081856 c.3561C>A p.P1187P Substitution - coding silent 6:78961785-78961785 - TCGA-DD-A1EB-01 COSM4928762 c.2770-1G>T p.? Unknown 6:78978712-78978712 - CSCC-55-T COSM4540876 c.2903G>A p.R968Q Substitution - Missense 6:78970875-78970875 - TCGA-B5-A0JY-01 COSM1081871 c.1068G>T p.E356D Substitution - Missense 6:79017510-79017510 - TCGA-AZ-4315-01 COSM170748 c.2925C>T p.V975V Substitution - coding silent 6:78970853-78970853 - NPC41F COSM4996758 c.5066C>G p.S1689C Substitution - Missense 6:78941093-78941093 - Sample_1 COSM4997675 c.341G>A p.S114N Substitution - Missense 6:79060576-79060576 - PT36 COSM5915567 c.2440A>T p.N814Y Substitution - Missense 6:78988229-78988229 - TCGA-85-6561-01 COSM743059 c.5348C>A p.S1783Y Substitution - Missense 6:78940811-78940811 - TCGA-EI-6917-01 COSM3175967 c.3707G>A p.R1236Q Substitution - Missense 6:78958550-78958550 - Au2 COSM5600203 c.5235G>A p.K1745K Substitution - coding silent 6:78940924-78940924 - TCGA-E2-A56Z-01 COSM3831102 c.2375A>T p.N792I Substitution - Missense 6:78988294-78988294 - TCGA-A4-8098-01 COSM3995130 c.1444C>T p.L482F Substitution - Missense 6:79015162-79015162 - YUKAT COSM5405869 c.3877C>T p.P1293S Substitution - Missense 6:78955258-78955258 - SNUH_G10_S1 COSM4004130 c.2621C>T p.T874I Substitution - Missense 6:78983034-78983034 - TCGA-EI-6513-01 COSM3430899 c.3928C>T p.R1310C Substitution - Missense 6:78954939-78954939 - 388 COSM98117 c.3301C>G p.Q1101E Substitution - Missense 6:78965961-78965961 - MO_1277 COSM5564101 c.3212G>A p.R1071H Substitution - Missense 6:78966050-78966050 - TCGA-G4-6628-01 COSM1446052 c.3675G>A p.M1225I Substitution - Missense 6:78958582-78958582 - TCGA-AA-A010-01 COSM283996 c.5131C>T p.R1711C Substitution - Missense 6:78941028-78941028 - TCGA-AN-A046-01 COSM3831101 c.4513C>T p.R1505* Substitution - Nonsense 6:78946118-78946118 - 2250155 COSM5029832 c.3706C>T p.R1236* Substitution - Nonsense 6:78958551-78958551 - CPCG0203-F1 COSM4880462 c.3180T>C p.D1060D Substitution - coding silent 6:78969860-78969860 - PD24204a COSM3430899 c.3928C>T p.R1310C Substitution - Missense 6:78954939-78954939 - TCGA-AD-6889-01 COSM1081844 c.4790C>T p.A1597V Substitution - Missense 6:78945338-78945338 - PD8621a COSM5802370 c.3155_3174del20 p.L1052fs*2 Deletion - Frameshift 6:78969866-78969885 - 587226 COSM1220393 c.1421C>T p.P474L Substitution - Missense 6:79015185-79015185 - ESO-887 COSM1262074 c.1133A>G p.N378S Substitution - Missense 6:79017349-79017349 - HT115 COSM3175975 c.3148G>T p.D1050Y Substitution - Missense 6:78969892-78969892 - PR-09-5094 COSM246568 c.5054A>C p.E1685A Substitution - Missense 6:78941105-78941105 - TCGA-B5-A0JY-01 COSM1081853 c.3753C>T p.F1251F Substitution - coding silent 6:78958504-78958504 - TCGA-AM-5820-01 COSM3762192 c.4236T>A p.A1412A Substitution - coding silent 6:78946845-78946845 - 35M COSM5582104 c.4021T>A p.F1341I Substitution - Missense 6:78954846-78954846 - Pat_06_B COSM5871143 c.2536A>G p.S846G Substitution - Missense 6:78985353-78985353 - TCGA-AA-A00N-01 COSM276731 c.3838T>G p.L1280V Substitution - Missense 6:78955627-78955627 - TCGA-BS-A0UL-01 COSM1081875 c.240T>C p.H80H Substitution - coding silent 6:79060768-79060768 - 2492701 COSM5600203 c.5235G>A p.K1745K Substitution - coding silent 6:78940924-78940924 - BD124T COSM5492107 c.1784G>A p.G595D Substitution - Missense 6:79001994-79001994 - TCGA-CA-6717-01 COSM1446044 c.4991A>C p.K1664T Substitution - Missense 6:78941168-78941168 - HCC171T COSM3662731 c.1829A>T p.E610V Substitution - Missense 6:79001949-79001949 - Gp5D COSM3175978 c.2959A>G p.N987D Substitution - Missense 6:78970819-78970819 - TCGA-D5-6928-01 COSM196940 c.2113G>A p.A705T Substitution - Missense 6:78997502-78997502 - HDC54 COSM4636497 c.1833T>C p.N611N Substitution - coding silent 6:79001945-79001945 - LUAD-F00368 COSM391756 c.2270_2297del28 p.R757fs*47 Deletion - Frameshift TCGA-46-6026-01 COSM743048 c.455C>T p.S152L Substitution - Missense 6:79042988-79042988 - UM-SCC-47 COSM3875670 c.3728G>A p.S1243N Substitution - Missense 6:78958529-78958529 - TCGA-BR-4184-01 COSM3875672 c.2466C>T p.G822G Substitution - coding silent 6:78985423-78985423 - CHC2216T COSM4805896 c.3617T>C p.L1206P Substitution - Missense 6:78961729-78961729 - TCGA-AG-4007-01 COSM289477 c.3326A>C p.N1109T Substitution - Missense 6:78965756-78965756 - T2269 COSM4714044 c.5436A>C p.E1812D Substitution - Missense 6:78940723-78940723 - tumor_4144951 COSM5948915 c.600+2T>A p.? Unknown 6:79042841-79042841 - ESCC_47 COSM5630796 c.2192G>C p.G731A Substitution - Missense 6:78997423-78997423 - TCGA-B2-5633-01 COSM484381 c.200A>G p.Y67C Substitution - Missense 6:79060808-79060808 - T3021 COSM4714053 c.190G>A p.V64M Substitution - Missense 6:79060818-79060818 - ME009T COSM223111 c.3560C>T p.P1187L Substitution - Missense 6:78961786-78961786 - TCGA-BP-5196-01 COSM484380 c.1920C>T p.I640I Substitution - coding silent 6:78998351-78998351 - TCGA-CJ-4905-01 COSM484378 c.5183A>C p.D1728A Substitution - Missense 6:78940976-78940976 - TCGA-A3-3316-01 COSM1496424 c.695C>G p.A232G Substitution - Missense 6:79026070-79026070 - TCGA-DM-A1DA-01 COSM1446062 c.288A>G p.G96G Substitution - coding silent 6:79060720-79060720 - 2292379 COSM4609928 c.1911C>A p.N637K Substitution - Missense 6:78998360-78998360 - TCGA-F5-6814-01 COSM3430901 c.1226G>A p.R409H Substitution - Missense 6:79016553-79016553 - LUAD-RT-S01702 COSM379390 c.2517G>T p.W839C Substitution - Missense 6:78985372-78985372 - sysucc-311T COSM5466926 c.2467G>A p.E823K Substitution - Missense 6:78985422-78985422 - TCGA-AA-A010-01 COSM283998 c.2390G>A p.R797H Substitution - Missense 6:78988279-78988279 - TCGA-B5-A11E-01 COSM1081839 c.5300G>A p.R1767K Substitution - Missense 6:78940859-78940859 - pfg143T COSM4758021 c.3893G>A p.R1298Q Substitution - Missense 6:78955242-78955242 - B88 COSM1754937 c.1607G>C p.G536A Substitution - Missense 6:79003776-79003776 - TCGA-D1-A17Q-01 COSM1081869 c.1187G>A p.R396Q Substitution - Missense 6:79016592-79016592 - E55 COSM1717591 c.2137G>T p.E713* Substitution - Nonsense 6:78997478-78997478 - HCT8 COSM4635435 c.1613T>C p.L538P Substitution - Missense 6:79003770-79003770 - 2474086 COSM5880233 c.4381A>G p.K1461E Substitution - Missense 6:78946250-78946250 - MEL-Ma-Mel-103b COSM1167850 c.1928_1929insT p.D644fs*18 Insertion - Frameshift 6:78998342-78998343 - HCC137T COSM5811285 c.5111A>G p.D1704G Substitution - Missense 6:78941048-78941048 - TCGA-60-2723-01 COSM743051 c.2196A>T p.V732V Substitution - coding silent 6:78997419-78997419 - HCC2998 COSM3175955 c.4602T>G p.A1534A Substitution - coding silent 6:78946029-78946029 - TCGA-ER-A19M-06 COSM3630088 c.163G>A p.E55K Substitution - Missense 6:79077474-79077474 - TCGA-66-2795-01 COSM743054 c.3424G>T p.G1142C Substitution - Missense 6:78963208-78963208 - HCC105 COSM1621963 c.4416A>T p.E1472D Substitution - Missense 6:78946215-78946215 - LUAD-F00368 COSM341452 c.3023G>T p.G1008V Substitution - Missense 6:78970148-78970148 - TCGA-33-6737-01 COSM743058 c.5046C>G p.I1682M Substitution - Missense 6:78941113-78941113 - TCGA-F4-6460-01 COSM1446050 c.3929G>A p.R1310H Substitution - Missense 6:78954938-78954938 - TCGA-BH-A18G-01 COSM3831103 c.2326G>A p.A776T Substitution - Missense 6:78988343-78988343 - RK029_C01 COSM1634944 c.1816G>C p.V606L Substitution - Missense 6:79001962-79001962 - TCGA-AA-A00N-01 COSM276732 c.2742A>C p.K914N Substitution - Missense 6:78982913-78982913 - TCGA-AP-A059-01 COSM1081840 c.5185C>A p.L1729I Substitution - Missense 6:78940974-78940974 - ESCC_57 COSM5632437 c.2905C>T p.Q969* Substitution - Nonsense 6:78970873-78970873 - pfg008T COSM1643149 c.4055A>G p.D1352G Substitution - Missense 6:78947774-78947774 - CSCC-20-T COSM4488586 c.3350C>T p.P1117L Substitution - Missense 6:78965732-78965732 - I2L-P7-Tumor-Organoid COSM5357762 c.441G>A p.A147A Substitution - coding silent 6:79043002-79043002 - 2011-2370:2012-1299-T COSM4604244 c.1301G>A p.R434Q Substitution - Missense 6:79015718-79015718 - TCGA-66-2770-01 COSM743050 c.1336A>G p.M446V Substitution - Missense 6:79015683-79015683 - TCGA-CD-8527-01 COSM3875676 c.1824C>T p.G608G Substitution - coding silent 6:79001954-79001954 - YULAN COSM1697565 c.2348T>G p.L783R Substitution - Missense 6:78988321-78988321 - 19M COSM5579314 c.4682C>T p.P1561L Substitution - Missense 6:78945446-78945446 - LUAD_E00565 COSM389580 c.1987G>T p.V663F Substitution - Missense 6:78998284-78998284 - TCGA-AA-3697-01 COSM1446046 c.4409A>T p.K1470I Substitution - Missense 6:78946222-78946222 - LS180 COSM3176006 c.1112T>C p.I371T Substitution - Missense 6:79017370-79017370 - TCGA-BR-8078-01 COSM3875673 c.2307C>A p.P769P Substitution - coding silent 6:78990880-78990880 - Pat_22_B COSM5871144 c.2288C>T p.P763L Substitution - Missense 6:78990899-78990899 - HT115 COSM3176004 c.1202G>A p.S401N Substitution - Missense 6:79016577-79016577 - RMS1_ COSM4985617 c.3418A>C p.T1140P Substitution - Missense 6:78963214-78963214 - TCGA-B5-A11N-01 COSM1081868 c.1330A>C p.N444H Substitution - Missense 6:79015689-79015689 - TCGA-EE-A3AF-06 COSM3630087 c.3623C>T p.T1208I Substitution - Missense 6:78961723-78961723 - CLN2 COSM5024783 c.1571C>A p.P524H Substitution - Missense 6:79003812-79003812 - SJRHB036A COSM3737224 c.610_611insACTA p.C205fs*1 Insertion - Frameshift 6:79026154-79026155 - 2_RESISTANT COSM1723222 c.4207-10delT p.? Unknown 6:78946884-78946884 - TCGA-AX-A0J1-01 COSM1081844 c.4790C>T p.A1597V Substitution - Missense 6:78945338-78945338 - GCT27 COSM5749394 c.2759G>C p.R920T Substitution - Missense 6:78982896-78982896 - TCGA-CA-6718-01 COSM1446047 c.4278A>C p.K1426N Substitution - Missense 6:78946803-78946803 - OSCC-GB_00680111 COSM1081853 c.3753C>T p.F1251F Substitution - coding silent 6:78958504-78958504 - 46M COSM5588631 c.2169G>T p.V723V Substitution - coding silent 6:78997446-78997446 - CN-AML-06-T COSM5428677 c.709A>T p.N237Y Substitution - Missense 6:79026056-79026056 - TCGA-DC-5337-01 COSM1568249 c.1153C>T p.R385C Substitution - Missense 6:79016626-79016626 - TCGA-CG-4442-01 COSM3875671 c.3256G>A p.E1086K Substitution - Missense 6:78966006-78966006 - 2474085 COSM5880233 c.4381A>G p.K1461E Substitution - Missense 6:78946250-78946250 - 587350 COSM1220394 c.1186C>T p.R396* Substitution - Nonsense 6:79016593-79016593 - TCGA-F1-6874-01 COSM3875674 c.2101A>T p.M701L Substitution - Missense 6:78997514-78997514 - 2250188 COSM4357132 c.2416C>T p.P806S Substitution - Missense 6:78988253-78988253 - TCGA-AX-A05Z-01 COSM1081845 c.4495G>T p.E1499* Substitution - Nonsense 6:78946136-78946136 - TCGA-AP-A059-01 COSM1081870 c.1136G>T p.R379M Substitution - Missense 6:79017346-79017346 - SC_9032 COSM5571848 c.2285T>A p.V762D Substitution - Missense 6:78990902-78990902 - pfg121T COSM4747540 c.1504delA p.I502fs*7 Deletion - Frameshift 6:79015102-79015102 - TCGA-RP-A694-06 COSM4894542 c.83G>A p.C28Y Substitution - Missense 6:79077871-79077871 - RK029_C COSM1634944 c.1816G>C p.V606L Substitution - Missense 6:79001962-79001962 - LCH-3 COSM5031133 c.380C>T p.A127V Substitution - Missense 6:79060537-79060537 - ASHPC_0010_Pa_P COSM4964777 c.2426C>T p.S809L Substitution - Missense 6:78988243-78988243 - TCGA-B5-A0K9-01 COSM1081866 c.1851C>A p.L617L Substitution - coding silent 6:79001927-79001927 - TCGA-QU-A6IM-01 COSM4393179 c.340A>T p.S114C Substitution - Missense 6:79060668-79060668 - OSCC-GB_01060111 COSM4882465 c.376G>T p.A126S Substitution - Missense 6:79060541-79060541 - TCGA-61-1910-01 COSM1329537 c.3788A>T p.Q1263L Substitution - Missense 6:78955677-78955677 - TCGA-CG-5721-01 COSM3875677 c.1406T>C p.V469A Substitution - Missense 6:79015200-79015200 - T2269 COSM283996 c.5131C>T p.R1711C Substitution - Missense 6:78941028-78941028 - 06-P036 COSM4586943 c.3423T>C p.D1141D Substitution - coding silent 6:78963209-78963209 - TCGA-66-2785-01 COSM743058 c.5046C>G p.I1682M Substitution - Missense 6:78941113-78941113 - TCGA-B5-A11N-01 COSM1081847 c.4448G>A p.R1483Q Substitution - Missense 6:78946183-78946183 - HCC2998 COSM1672580 c.1378C>A p.H460N Substitution - Missense 6:79015641-79015641 - SNU-175 COSM3176003 c.1382T>C p.V461A Substitution - Missense 6:79015637-79015637 - sysucc-1397T COSM1220394 c.1186C>T p.R396* Substitution - Nonsense 6:79016593-79016593 - TCGA-BR-8081-01 COSM3875679 c.510T>C p.Y170Y Substitution - coding silent 6:79042933-79042933 - TCGA-AB-2967-03 COSM1319061 c.3947_3948insA p.Y1316fs*1 Insertion - Frameshift 6:78954919-78954920 - Co79 COSM33476 c.5300G>T p.R1767I Substitution - Missense 6:78940859-78940859 - SC_9028 COSM5564705 c.5142G>A p.R1714R Substitution - coding silent 6:78941017-78941017 - TCGA-D1-A163-01 COSM1081846 c.4486G>A p.G1496S Substitution - Missense 6:78946145-78946145 - Gp2D COSM3175978 c.2959A>G p.N987D Substitution - Missense 6:78970819-78970819 - TCGA-CS-5390-01 COSM3928620 c.4895C>G p.S1632* Substitution - Nonsense 6:78941264-78941264 - TCGA-AZ-4315-01 COSM1446056 c.1261A>C p.K421Q Substitution - Missense 6:79015758-79015758 - TCGA-D1-A16X-01 COSM176342 c.4584G>T p.K1528N Substitution - Missense 6:78946047-78946047 - PT40 COSM4473799 c.1874C>T p.S625F Substitution - Missense 6:79001904-79001904 - PT37 COSM5919068 c.1819C>T p.P607S Substitution - Missense 6:79001959-79001959 - LUAD-D02185 COSM338824 c.2970A>G p.K990K Substitution - coding silent 6:78970808-78970808 - TCGA-24-1544-01 COSM82288 c.4746A>G p.E1582E Substitution - coding silent 6:78945382-78945382 - TCGA-EL-A3CZ-01 COSM3374386 c.2095C>T p.R699W Substitution - Missense 6:78997520-78997520 - TCGA-BR-4184-01 COSM3875675 c.1910A>C p.N637T Substitution - Missense 6:78998361-78998361 - LUAD-D01751 COSM338368 c.375G>T p.L125L Substitution - coding silent 6:79060542-79060542 - LAU165 COSM235195 c.2964C>T p.P988P Substitution - coding silent 6:78970814-78970814 - TCGA-BR-8372-01 COSM3875678 c.1168C>T p.R390C Substitution - Missense 6:79016611-79016611 - ESO-H01 COSM1262075 c.3363G>A p.E1121E Substitution - coding silent 6:78965719-78965719 - RK135_C01 COSM1446050 c.3929G>A p.R1310H Substitution - Missense 6:78954938-78954938 - TCGA-E9-A1RF-01 COSM1487942 c.1292C>A p.A431D Substitution - Missense 6:79015727-79015727 - LPJ108 COSM1316292 c.2033C>T p.T678I Substitution - Missense 6:78997582-78997582 - Mx41 COSM32396 c.1405G>A p.V469I Substitution - Missense 6:79015201-79015201 - CSCC-40-T COSM4482455 c.2609C>T p.P870L Substitution - Missense 6:78983046-78983046 - 51 COSM5734595 c.1511C>G p.S504C Substitution - Missense 6:79015095-79015095 - T3094 COSM4714052 c.444T>C p.D148D Substitution - coding silent 6:79042999-79042999 - Br04X COSM39331 c.4031C>T p.P1344L Substitution - Missense 6:78954836-78954836 - tumor_4144951 COSM5948939 c.600+3A>T p.? Unknown 6:79042840-79042840 - TCGA-AX-A05Z-01 COSM1081857 c.3503T>G p.I1168S Substitution - Missense 6:78963129-78963129 - HN_63021 COSM125342 c.5401A>G p.T1801A Substitution - Missense 6:78940758-78940758 - TCGA-AB-2897-03 COSM1319060 c.630G>T p.W210C Substitution - Missense 6:79026135-79026135 - TCGA-AZ-6598-01 COSM1446059 c.487C>T p.R163* Substitution - Nonsense 6:79042956-79042956 - TCGA-BS-A0UM-01 COSM1081850 c.3874G>A p.V1292M Substitution - Missense 6:78955261-78955261 - CHC2216T COSM4805896 c.3617T>C p.L1206P Substitution - Missense 6:78961729-78961729 - CSCC-60-T COSM4473799 c.1874C>T p.S625F Substitution - Missense 6:79001904-79001904 - T3262 COSM4714051 c.1050delT p.F350fs*32 Deletion - Frameshift 6:79017528-79017528 - Gp5D COSM3175972 c.3209A>G p.D1070G Substitution - Missense 6:78966053-78966053 - CRC-02T COSM5455523 c.3237C>A p.A1079A Substitution - coding silent 6:78966025-78966025 - MO_1012 COSM5571863 c.2313C>T p.V771V Substitution - coding silent 6:78990874-78990874 - TCGA-AM-5820-01 COSM3762194 c.3278T>C p.L1093P Substitution - Missense 6:78965984-78965984 - MOLT-4 COSM1672579 c.4136T>C p.M1379T Substitution - Missense 6:78947693-78947693 - TCGA-D1-A17D-01 COSM1081852 c.3754G>A p.V1252M Substitution - Missense 6:78958503-78958503 - PCSI_0121_Pa_P COSM3381670 c.4999C>T p.Q1667* Substitution - Nonsense 6:78941160-78941160 - ESO-250 COSM1262073 c.14G>A p.R5K Substitution - Missense 6:79078055-79078055 - TCGA-LG-A6GG-01 COSM4939508 c.2781G>C p.V927V Substitution - coding silent 6:78978700-78978700 - TCGA-D1-A177-01 COSM1081841 c.4901T>G p.L1634R Substitution - Missense 6:78941258-78941258 - 193 COSM1741812 c.3088A>G p.T1030A Substitution - Missense 6:78970083-78970083 - TCGA-BS-A0TC-01 COSM1081849 c.4018C>T p.P1340S Substitution - Missense 6:78954849-78954849 - TCGA-F5-6814-01 COSM3430900 c.1508G>A p.R503Q Substitution - Missense 6:79015098-79015098 - 587342 COSM1220396 c.995-1G>A p.? Unknown 6:79017584-79017584 - CN-AML-15-T COSM5427326 c.3468G>A p.W1156* Substitution - Nonsense 6:78963164-78963164 - CN-AML-NR-06-Dx COSM5428677 c.709A>T p.N237Y Substitution - Missense 6:79026056-79026056 - 2492702 COSM5600203 c.5235G>A p.K1745K Substitution - coding silent 6:78940924-78940924 - TCGA-EI-6917-01 COSM1081869 c.1187G>A p.R396Q Substitution - Missense 6:79016592-79016592 - TCGA-BS-A0UV-01 COSM1081860 c.3193C>T p.R1065* Substitution - Nonsense 6:78969847-78969847 - LUAD-E01278 COSM394329 c.62G>T p.R21L Substitution - Missense 6:79077892-79077892 - TCGA-AA-A010-01 COSM283997 c.2755G>T p.E919* Substitution - Nonsense 6:78982900-78982900 - TCGA-UB-A7MB-01 COSM4932502 c.4168A>T p.S1390C Substitution - Missense 6:78947661-78947661 - TCGA-E2-A1B1-01 COSM451824 c.3831_3833delGAA p.K1278delK Deletion - In frame 6:78955632-78955634 - TCGA-D8-A1J8-01 COSM3831104 c.1383C>G p.V461V Substitution - coding silent 6:79015636-79015636 - Gp2D COSM3175972 c.3209A>G p.D1070G Substitution - Missense 6:78966053-78966053 - 478 COSM4438985 c.1013C>T p.T338M Substitution - Missense 6:79017565-79017565 - TCGA-D1-A174-01 COSM1081861 c.3182C>T p.A1061V Substitution - Missense 6:78969858-78969858 - TCGA-AA-3715-01 COSM269879 c.3288T>C p.P1096P Substitution - coding silent 6:78965974-78965974 - CSCC-44-T COSM4473510 c.1855C>T p.P619S Substitution - Missense 6:79001923-79001923 - NPCPR15 COSM4996757 c.5279A>G p.K1760R Substitution - Missense 6:78940880-78940880 - OSCC-GB_00890111 COSM4887500 c.3952A>G p.I1318V Substitution - Missense 6:78954915-78954915 - TCGA-CG-5733-01 COSM3875667 c.4514G>A p.R1505Q Substitution - Missense 6:78946117-78946117 - 2492703 COSM5600203 c.5235G>A p.K1745K Substitution - coding silent 6:78940924-78940924 - YUPROST COSM1697564 c.5146C>T p.P1716S Substitution - Missense 6:78941013-78941013 - TCGA-B5-A11E-01 COSM1081853 c.3753C>T p.F1251F Substitution - coding silent 6:78958504-78958504 - SNU-175 COSM3176010 c.721G>A p.A241T Substitution - Missense 6:79026044-79026044 - TCGA-AX-A05Z-01 COSM1081858 c.3406A>G p.S1136G Substitution - Missense 6:78963226-78963226 - sysucc-1317T COSM5450284 c.4706G>C p.G1569A Substitution - Missense 6:78945422-78945422 - TCGA-B5-A11E-01 COSM1081872 c.874G>T p.D292Y Substitution - Missense 6:79025568-79025568 - TCGA-DD-A39Z-01 COSM4915923 c.2667A>G p.K889K Substitution - coding silent 6:78982988-78982988 - LS174T COSM3176006 c.1112T>C p.I371T Substitution - Missense 6:79017370-79017370 - SNUH_G45_S1 COSM4004130 c.2621C>T p.T874I Substitution - Missense 6:78983034-78983034 - 2324292 COSM3762194 c.3278T>C p.L1093P Substitution - Missense 6:78965984-78965984 - 2492700 COSM5600203 c.5235G>A p.K1745K Substitution - coding silent 6:78940924-78940924 - CSCC-20-T COSM4498378 c.5194C>T p.P1732S Substitution - Missense 6:78940965-78940965 - TCGA-HC-A6AO-01 COSM4392294 c.2581A>T p.I861F Substitution - Missense 6:78983074-78983074 - YUROC COSM5405870 c.3444C>T p.I1148I Substitution - coding silent 6:78963188-78963188 - ICGC_0059 COSM1159395 c.1428G>A p.P476P Substitution - coding silent 6:79015178-79015178 - SJDES007-R1 COSM4586941 c.4639A>C p.N1547H Substitution - Missense 6:78945489-78945489 - RK187_C01 COSM3745369 c.5172A>G p.K1724K Substitution - coding silent 6:78940987-78940987 - TCGA-66-2744-01 COSM743053 c.2873C>A p.P958Q Substitution - Missense 6:78978608-78978608 - T14 COSM5617858 c.4786A>G p.K1596E Substitution - Missense 6:78945342-78945342 - TCGA-BS-A0UV-01 COSM1081874 c.764G>A p.R255Q Substitution - Missense 6:79026001-79026001 - TCGA-B5-A0JY-01 COSM1081848 c.4382A>C p.K1461T Substitution - Missense 6:78946249-78946249 - TCGA-B5-A11E-01 COSM1081862 c.2926G>A p.E976K Substitution - Missense 6:78970852-78970852 - T2940 COSM4714049 c.1687C>T p.R563W Substitution - Missense 6:79002091-79002091 - PD6650a COSM3719982 c.1606G>T p.G536* Substitution - Nonsense 6:79003777-79003777 - QC2-34-T2 COSM5654762 c.153G>C p.W51C Substitution - Missense 6:79077484-79077484 - LS411 COSM196940 c.2113G>A p.A705T Substitution - Missense 6:78997502-78997502 - 046T COSM1729799 c.1136+1G>A p.? Unknown 6:79017345-79017345 - HX36T COSM1621962 c.4643C>G p.S1548C Substitution - Missense 6:78945485-78945485 - SC_9047 COSM5557366 c.1698T>C p.I566I Substitution - coding silent 6:79002080-79002080 - TCGA-AP-A0LM-01 COSM1081873 c.822+1G>A p.? Unknown 6:79025942-79025942 - 9210_T COSM5040730 c.4264T>G p.L1422V Substitution - Missense 6:78946817-78946817 - TCGA-BR-4362-01 COSM3875666 c.4706G>A p.G1569D Substitution - Missense 6:78945422-78945422 - 49M COSM5592505 c.2020T>C p.S674P Substitution - Missense 6:78997595-78997595 - EGC15 COSM283998 c.2390G>A p.R797H Substitution - Missense 6:78988279-78988279 - TCGA-BH-A0HP-01 COSM451825 c.3457G>A p.D1153N Substitution - Missense 6:78963175-78963175 - TCGA-UB-A7MB-01 COSM4931429 c.433A>T p.S145C Substitution - Missense 6:79060484-79060484 - TCGA-BR-4361-01 COSM1568249 c.1153C>T p.R385C Substitution - Missense 6:79016626-79016626 - TCGA-BR-8680-01 COSM3875669 c.4263T>G p.V1421V Substitution - coding silent 6:78946818-78946818 - TCGA-B5-A11R-01 COSM1081859 c.3289G>C p.D1097H Substitution - Missense 6:78965973-78965973 - 8030340 COSM1159395 c.1428G>A p.P476P Substitution - coding silent 6:79015178-79015178 - OSCC-GB_00960111 COSM4885608 c.2286T>A p.V762V Substitution - coding silent 6:78990901-78990901 - RK027_C01 COSM1634943 c.1918A>G p.I640V Substitution - Missense 6:78998353-78998353 - ZZUFHECRKL-G038T COSM5442545 c.760C>G p.L254V Substitution - Missense 6:79026005-79026005 - TCGA-EE-A29D-06 COSM3630086 c.3982T>C p.L1328L Substitution - coding silent 6:78954885-78954885 - T2950 COSM4714045 c.5255A>G p.E1752G Substitution - Missense 6:78940904-78940904 - YURAY COSM5405868 c.4715A>T p.N1572I Substitution - Missense 6:78945413-78945413 - TCGA-B5-A0JY-01 COSM1081865 c.1889A>C p.Q630P Substitution - Missense 6:78998382-78998382 - tumor_4190495 COSM1161640 c.609T>G p.D203E Substitution - Missense 6:79026156-79026156 - TCGA-BR-7197-01 COSM3430899 c.3928C>T p.R1310C Substitution - Missense 6:78954939-78954939 - PT34 COSM3430899 c.3928C>T p.R1310C Substitution - Missense 6:78954939-78954939 - TCGA-18-3419-01 COSM743055 c.3520C>A p.Q1174K Substitution - Missense 6:78963112-78963112 - SC_9032 COSM5563251 c.3940C>T p.Q1314* Substitution - Nonsense 6:78954927-78954927 - TCGA-AX-A0J0-01 COSM276731 c.3838T>G p.L1280V Substitution - Missense 6:78955627-78955627 - TCGA-EI-6508-01 COSM1568252 c.5113T>G p.L1705V Substitution - Missense 6:78941046-78941046 - BL4 COSM1161640 c.609T>G p.D203E Substitution - Missense 6:79026156-79026156 - TCGA-BR-4184-01 COSM3875670 c.3728G>A p.S1243N Substitution - Missense 6:78958529-78958529 - TCGA-20-1685-01 COSM1329536 c.2312T>C p.V771A Substitution - Missense 6:78990875-78990875 - CN-AML-08-T COSM3762194 c.3278T>C p.L1093P Substitution - Missense 6:78965984-78965984 - CSCC-44-T COSM4546956 c.4111G>C p.E1371Q Substitution - Missense 6:78947718-78947718 - PT48 COSM5931872 c.2044C>T p.H682Y Substitution - Missense 6:78997571-78997571 - TCGA-CD-8526-01 COSM3875668 c.4513C>G p.R1505G Substitution - Missense 6:78946118-78946118 - TCGA-AD-6964-01 COSM3686351 c.3657-4delT p.? Unknown 6:78958604-78958604 - 229 COSM4426334 c.5362A>G p.R1788G Substitution - Missense 6:78940797-78940797 - HCC105T COSM1621963 c.4416A>T p.E1472D Substitution - Missense 6:78946215-78946215 - PD7437a COSM3720216 c.3677G>A p.W1226* Substitution - Nonsense 6:78958580-78958580 - 15145 COSM743052 c.2202-3C>T p.? Unknown 6:78990988-78990988 - TCGA-D5-6540-01 COSM1446055 c.2105A>T p.H702L Substitution - Missense 6:78997510-78997510 - C0020T COSM4155298 c.5062C>G p.P1688A Substitution - Missense 6:78941097-78941097 - TCGA-C4-A0F1-01 COSM421227 c.1027C>T p.H343Y Substitution - Missense 6:79017551-79017551 - T3064 COSM4714046 c.3383T>C p.V1128A Substitution - Missense 6:78963249-78963249 - GCT57 COSM5749868 c.3059G>A p.C1020Y Substitution - Missense 6:78970112-78970112 - TCGA-A5-A0GH-01 COSM1081867 c.1642A>G p.K548E Substitution - Missense 6:79003741-79003741 - MO_1012 COSM5555350 c.1058G>A p.G353D Substitution - Missense 6:79017520-79017520 - HCC171 COSM3662731 c.1829A>T p.E610V Substitution - Missense 6:79001949-79001949 - TCGA-C8-A12T-01 COSM451826 c.2887G>A p.E963K Substitution - Missense 6:78978594-78978594 - CPCG0203-F1 COSM4880444 c.4155C>T p.V1385V Substitution - coding silent 6:78947674-78947674 - TCGA-CA-6717-01 COSM3698011 c.338A>C p.K113T Substitution - Missense 6:79060670-79060670 - TCGA-DK-A1A7-01 COSM421228 c.4700G>C p.S1567T Substitution - Missense 6:78945428-78945428 - TCGA-AA-3492-01 COSM1446053 c.3148G>A p.D1050N Substitution - Missense 6:78969892-78969892 - TCGA-AA-3510-01 COSM1081874 c.764G>A p.R255Q Substitution - Missense 6:79026001-79026001 - 2171751 COSM1081868 c.1330A>C p.N444H Substitution - Missense 6:79015689-79015689 - TCGA-AD-6964-01 COSM1446051 c.3783-2A>G p.? Unknown 6:78955684-78955684 - B88-Tumor COSM1754937 c.1607G>C p.G536A Substitution - Missense 6:79003776-79003776 - T55 COSM4714050 c.1545C>T p.G515G Substitution - coding silent 6:79003838-79003838 - T3724 COSM4714047 c.3264G>A p.Q1088Q Substitution - coding silent 6:78965998-78965998 - 2011-2318:2012-356-T COSM4604000 c.1041T>G p.V347V Substitution - coding silent 6:79017537-79017537 - TCGA-AM-5820-01 COSM3762193 c.4228C>T p.L1410L Substitution - coding silent 6:78946853-78946853 - TCGA-AG-3742-01 COSM1568250 c.2585A>G p.N862S Substitution - Missense 6:78983070-78983070 - RKO COSM4649020 c.2430A>G p.E810E Substitution - coding silent 6:78988239-78988239 - CHEWS007 COSM4586942 c.3805A>G p.I1269V Substitution - Missense 6:78955660-78955660 - Br09P COSM39640 c.737A>G p.D246G Substitution - Missense 6:79026028-79026028 - TCGA-A8-A09Z-01 COSM269879 c.3288T>C p.P1096P Substitution - coding silent 6:78965974-78965974 - TCGA-B5-A0JY-01 COSM1081864 c.2026A>C p.S676R Substitution - Missense 6:78997589-78997589 - MO_1012 COSM3686351 c.3657-4delT p.? Unknown 6:78958604-78958604 - HCC027T COSM5811707 c.682A>C p.I228L Substitution - Missense 6:79026083-79026083 - TCGA-BT-A20N-01 COSM421229 c.5298G>C p.M1766I Substitution - Missense 6:78940861-78940861 - PR-04-3347 COSM246567 c.2258C>A p.S753* Substitution - Nonsense 6:78990929-78990929 - BK0019 COSM4186138 c.1937T>C p.M646T Substitution - Missense 6:78998334-78998334 - TCGA-BS-A0UJ-01 COSM1081843 c.4810T>C p.S1604P Substitution - Missense 6:78945318-78945318 - LUAD-S00499 COSM385374 c.3981A>C p.E1327D Substitution - Missense 6:78954886-78954886 - 4 COSM5732101 c.275A>G p.Q92R Substitution - Missense 6:79060733-79060733 - T3021 COSM4714048 c.2569G>A p.A857T Substitution - Missense 6:78983086-78983086 - C037 COSM5524455 c.863C>T p.S288F Substitution - Missense 6:79025579-79025579 - LIM1215 COSM1159395 c.1428G>A p.P476P Substitution - coding silent 6:79015178-79015178 - ESCC-185T COSM3941849 c.4189C>G p.P1397A Substitution - Missense 6:78947640-78947640 - pfg008T COSM1643149 c.4055A>G p.D1352G Substitution - Missense 6:78947774-78947774 - RMS88_ COSM4988896 c.5284T>C p.S1762P Substitution - Missense 6:78940875-78940875 - TCGA-AP-A0LM-01 COSM1081855 c.3686G>A p.R1229Q Substitution - Missense 6:78958571-78958571 - SNUH_G10_S1 COSM3762194 c.3278T>C p.L1093P Substitution - Missense 6:78965984-78965984 - 10T COSM3430899 c.3928C>T p.R1310C Substitution - Missense 6:78954939-78954939 - HCC29T COSM1621962 c.4643C>G p.S1548C Substitution - Missense 6:78945485-78945485 - TCGA-BK-A0C9-01 COSM1081863 c.2093T>A p.V698E Substitution - Missense 6:78997522-78997522 - PD4194a COSM219580 c.1285A>G p.M429V Substitution - Missense 6:79015734-79015734 - 1N66-VS-1T66 COSM4978221 c.1402G>T p.E468* Substitution - Nonsense 6:79015204-79015204 - TCGA-61-1725-01 COSM1329538 c.4971G>A p.K1657K Substitution - coding silent 6:78941188-78941188 - TCGA-B5-A11E-01 COSM1081869 c.1187G>A p.R396Q Substitution - Missense 6:79016592-79016592 - TCGA-39-5022-01 COSM743056 c.4520G>A p.R1507K Substitution - Missense 6:78946111-78946111 - HCC29 COSM1621962 c.4643C>G p.S1548C Substitution - Missense 6:78945485-78945485 - OSCC-GB_00670111 COSM4883931 c.2923G>A p.V975I Substitution - Missense 6:78970855-78970855 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.511817 6q14 612870 Hs.606356 6q14 612870

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.D203E c.609T>G 6 79735873 DLBCL A C Missense p.L1634R c.4901T>G 6 79650975 UCEC - A Frameshift p.D644Gfs*18 c.1928dupT 6 79708060 CM A G Missense p.D246G c.737A>G 6 79735745 GBM A G Synonymous p.H80H c.240T>C 6 79770485 UCEC C A Missense p.A1061S c.3181G>T 6 79679576 HNSC C A Missense p.G1142C c.3424G>T 6 79672925 LUSC C A Missense p.G215W c.643G>T 6 79735839 STAD C A Missense p.R81L c.242G>T 6 79770483 LUAD C A Missense p.W210C c.630G>T 6 79735852 AML C G Missense p.D1097H c.3289G>C 6 79675690 UCEC C G Missense p.M1766I c.5298G>C 6 79650578 BLCA C G Missense p.S1567T c.4700G>C 6 79655145 BLCA C G Missense p.V606L c.1816G>C 6 79711679 HC C T IntronicSNV . c.2770-1241G>A 6 79689669 CLL C T Missense p.A705T c.2113G>A 6 79707219 SCLC C T Missense p.D1153N c.3457G>A 6 79672892 BRCA C T Missense p.E963K c.2887G>A 6 79688311 BRCA C T Missense p.P1344L c.4031C>T 6 79664553 GBM C T Missense p.R1505Q c.4514G>A 6 79655834 STAD C T Missense p.R1507K c.4520G>A 6 79655828 LUSC C T Missense p.R5K c.14G>A 6 79787772 ESCA C T Missense p.R797H c.2390G>A 6 79697996 HNSC C T Missense p.V1252M c.3754G>A 6 79668220 UCEC C T SpliceDonorSNV . c.2460+1G>A 6 79697925 LUAD C T Synonymous p.A127A c.381G>A 6 79770253 STAD C T Synonymous p.E1121E c.3363G>A 6 79675436 ESCA C T Synonymous p.P476P c.1428G>A 6 79724895 PAAD G A IntronicSNV . c.2202-3C>T 6 79700705 NSCLC G A Missense p.H343Y c.1027C>T 6 79727268 BLCA G A Missense p.P1187L c.3560C>T 6 79671503 CM G A Missense p.P1340S c.4018C>T 6 79664566 UCEC G A Missense p.R699W c.2095C>T 6 79707237 THCA G A Missense p.S152L c.455C>T 6 79752705 LUSC G A Missense p.T1208I c.3623C>T 6 79671440 CM G A Missense p.T59I c.176C>T 6 79787178 HNSC G A Missense p.V469I c.1405G>A 6 79724918 COREAD G A Nonsense p.R1229* c.3685C>T 6 79668289 HNSC G A Nonsense p.R1773* c.5317C>T 6 79650559 COREAD G A Synonymous p.I640I c.1920C>T 6 79708068 RCCC G A Synonymous p.S832S c.2496C>T 6 79695110 STAD G C IntronicSNV . c.4371-59C>G 6 79656036 ESCA G C Missense p.I1682M c.5046C>G 6 79650830 LUSC G C Missense p.Q1493E c.4477C>G 6 79655871 HNSC G C Nonsense p.S1632* c.4895C>G 6 79650981 LGG G C Synonymous p.L299L c.897C>G 6 79735262 LUAD GG AA Missense p.P1244S c.3729_3730delinsTT 6 79668244 CM GG AA Missense p.P1732F c.5194_5195delinsTT 6 79650681 CM G T Missense p.A431D c.1292C>A 6 79725444 BRCA G T Missense p.P958Q c.2873C>A 6 79688325 LUSC G T Missense p.Q1174K c.3520C>A 6 79672829 CM G T Missense p.Q1174K c.3520C>A 6 79672829 LUSC G T Missense p.R110S c.328C>A 6 79770397 HNSC G T Missense p.R1767I c.5300G>T 6 79650576 COREAD G T Missense p.S1783Y c.5348C>A 6 79650528 LUSC G T Synonymous p.G511G c.1533C>A 6 79713567 STAD G T Synonymous p.R1808R c.5422C>A 6 79650454 CM T A Missense p.I861F c.2581A>T 6 79692791 PRAD T A Missense p.M621L c.1861A>T 6 79711634 HNSC T A Missense p.M701L c.2101A>T 6 79707231 STAD T A Missense p.S114C c.340A>T 6 79770385 PRAD T A Synonymous p.V732V c.2196A>T 6 79707136 LUSC T C IntronicSNV . c.3782+68A>G 6 79668124 HC T C Missense p.D1352G c.4055A>G 6 79657491 STAD T C Missense p.I640V c.1918A>G 6 79708070 HC T C Missense p.K548E c.1642A>G 6 79713458 UCEC T C Missense p.M446V c.1336A>G 6 79725400 LUSC T C Missense p.N378S c.1133A>G 6 79727066 ESCA T C Missense p.S547G c.1639A>G 6 79713461 PRAD T C Missense p.T1801A c.5401A>G 6 79650475 HNSC T C Synonymous p.E1582E c.4746A>G 6 79655099 OV T G Missense p.D1728A c.5183A>C 6 79650693 RCCC T G Missense p.N1109T c.3326A>C 6 79675473 COREAD - T Nonsense p.Y1316*fs*1 c.3947dupA 6 79664637 AML TTC - InFrameDeletion p.K1278delK c.3831_3833delGAA 6 79665349 BRCA