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 3 101370486 101370486 + Missense_Mutation SNP C C T TCGA-BT-A20P-01A-11D-A14W-08 TCGA-BT-A20P-11A-11D-A14W-08 g.chr3:101370486C>T c.2686G>A c.(2686-2688)Gct>Act p.A896T BLCA 3 101373573 101373573 + Missense_Mutation SNP C C T TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr3:101373573C>T c.2284G>A c.(2284-2286)Gag>Aag p.E762K BLCA 3 101378715 101378715 + Missense_Mutation SNP C C T TCGA-GD-A2C5-01A-12D-A17V-08 TCGA-GD-A2C5-10A-01D-A17V-08 g.chr3:101378715C>T c.1958G>A c.(1957-1959)tGt>tAt p.C653Y BLCA 3 101378760 101378760 + Missense_Mutation SNP G G A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr3:101378760G>A c.1913C>T c.(1912-1914)tCg>tTg p.S638L BLCA 3 101383486 101383486 + Missense_Mutation SNP C C T TCGA-GU-AATO-01A-11D-A391-08 TCGA-GU-AATO-10A-01D-A394-08 g.chr3:101383486C>T c.1696G>A c.(1696-1698)Gaa>Aaa p.E566K BLCA 3 101384254 101384254 + Missense_Mutation SNP C C T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr3:101384254C>T c.1177G>A c.(1177-1179)Gaa>Aaa p.E393K BLCA 3 101390034 101390034 + Nonsense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr3:101390034G>A c.718C>T c.(718-720)Cga>Tga p.R240* BLCA 3 101390113 101390113 + Silent SNP G G A TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr3:101390113G>A c.639C>T c.(637-639)ttC>ttT p.F213F BLCA 3 101391041 101391041 + Silent SNP G G C TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr3:101391041G>C c.327C>G c.(325-327)gtC>gtG p.V109V BLCA 3 101395550 101395550 + Missense_Mutation SNP C C T TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr3:101395550C>T c.209G>A c.(208-210)cGa>cAa p.R70Q BRCA 3 101370304 101370304 + Silent SNP G G A TCGA-D8-A1JK-01A-11D-A13L-09 TCGA-D8-A1JK-10A-01D-A13O-09 g.chr3:101370304G>A c.2868C>T c.(2866-2868)aaC>aaT p.N956N BRCA 3 101370349 101370349 + Silent SNP C C T TCGA-D8-A1XW-01A-11D-A14K-09 TCGA-D8-A1XW-10A-01D-A14K-09 g.chr3:101370349C>T c.2823G>A c.(2821-2823)gtG>gtA p.V941V BRCA 3 101370392 101370392 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr3:101370392C>T c.2780G>A c.(2779-2781)cGa>cAa p.R927Q BRCA 3 101375072 101375072 + Missense_Mutation SNP G G C TCGA-B6-A1KN-01A-11D-A13L-09 TCGA-B6-A1KN-10A-01D-A188-09 g.chr3:101375072G>C c.2067C>G c.(2065-2067)atC>atG p.I689M BRCA 3 101378855 101378855 + Missense_Mutation SNP A A C TCGA-A1-A0SJ-01A-11D-A099-09 TCGA-A1-A0SJ-10A-02D-A099-09 g.chr3:101378855A>C c.1818T>G c.(1816-1818)ttT>ttG p.F606L CESC 3 101374961 101374961 + Missense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr3:101374961C>G c.2178G>C c.(2176-2178)atG>atC p.M726I CESC 3 101383876 101383876 + Nonsense_Mutation SNP G G A TCGA-FU-A3YQ-01A-11D-A22X-09 TCGA-FU-A3YQ-10A-01D-A22X-09 g.chr3:101383876G>A c.1555C>T c.(1555-1557)Cga>Tga p.R519* CESC 3 101384145 101384145 + Missense_Mutation SNP C C G TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr3:101384145C>G c.1286G>C c.(1285-1287)aGa>aCa p.R429T CHOL 3 101395620 101395620 + Missense_Mutation SNP G G C TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr3:101395620G>C c.139C>G c.(139-141)Ctg>Gtg p.L47V COAD 3 101370011 101370011 + Nonstop_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:101370011C>A c.3161G>T c.(3160-3162)tGa>tTa p.*1054L COAD 3 101370080 101370080 + Missense_Mutation SNP T T G TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr3:101370080T>G c.3092A>C c.(3091-3093)aAg>aCg p.K1031T COAD 3 101370318 101370318 + Missense_Mutation SNP G G T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:101370318G>T c.2854C>A c.(2854-2856)Ctt>Att p.L952I COAD 3 101378657 101378657 + Missense_Mutation SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr3:101378657C>A c.2016G>T c.(2014-2016)aaG>aaT p.K672N COAD 3 101378774 101378774 + Silent SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr3:101378774C>T c.1899G>A c.(1897-1899)acG>acA p.T633T COAD 3 101383435 101383435 + Missense_Mutation SNP C C T TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr3:101383435C>T c.1747G>A c.(1747-1749)Gcc>Acc p.A583T COAD 3 101384048 101384048 + Silent SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:101384048T>C c.1383A>G c.(1381-1383)tcA>tcG p.S461S COAD 3 101384352 101384352 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:101384352T>C c.1079A>G c.(1078-1080)gAt>gGt p.D360G COAD 3 101384531 101384531 + Silent SNP G G T TCGA-AA-3976-01A-01W-0995-10 TCGA-AA-3976-10A-01W-0999-10 g.chr3:101384531G>T c.900C>A c.(898-900)gtC>gtA p.V300V COADREAD 3 101370011 101370011 + Nonstop_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:101370011C>A c.3161G>T c.(3160-3162)tGa>tTa p.*1054L COADREAD 3 101370080 101370080 + Missense_Mutation SNP T T G TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr3:101370080T>G c.3092A>C c.(3091-3093)aAg>aCg p.K1031T COADREAD 3 101370201 101370201 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:101370201C>A c.2971G>T c.(2971-2973)Gaa>Taa p.E991* COADREAD 3 101370318 101370318 + Missense_Mutation SNP G G T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:101370318G>T c.2854C>A c.(2854-2856)Ctt>Att p.L952I COADREAD 3 101373592 101373592 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:101373592C>A c.2265G>T c.(2263-2265)aaG>aaT p.K755N COADREAD 3 101374975 101374975 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:101374975G>T c.2164C>A c.(2164-2166)Ctt>Att p.L722I COADREAD 3 101378657 101378657 + Missense_Mutation SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr3:101378657C>A c.2016G>T c.(2014-2016)aaG>aaT p.K672N COADREAD 3 101378774 101378774 + Silent SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr3:101378774C>T c.1899G>A c.(1897-1899)acG>acA p.T633T COADREAD 3 101383435 101383435 + Missense_Mutation SNP C C T TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr3:101383435C>T c.1747G>A c.(1747-1749)Gcc>Acc p.A583T COADREAD 3 101384048 101384048 + Silent SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:101384048T>C c.1383A>G c.(1381-1383)tcA>tcG p.S461S COADREAD 3 101384352 101384352 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:101384352T>C c.1079A>G c.(1078-1080)gAt>gGt p.D360G COADREAD 3 101384531 101384531 + Silent SNP G G T TCGA-AA-3976-01A-01W-0995-10 TCGA-AA-3976-10A-01W-0999-10 g.chr3:101384531G>T c.900C>A c.(898-900)gtC>gtA p.V300V DLBC 3 101370091 101370091 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr3:101370091C>T c.3081G>A c.(3079-3081)caG>caA p.Q1027Q ESCA 3 101370141 101370141 + Missense_Mutation SNP G G A TCGA-L5-A4OP-01A-11D-A27G-09 TCGA-L5-A4OP-11A-11D-A27G-09 g.chr3:101370141G>A c.3031C>T c.(3031-3033)Ctt>Ttt p.L1011F ESCA 3 101371366 101371366 + Missense_Mutation SNP T T A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr3:101371366T>A c.2618A>T c.(2617-2619)tAt>tTt p.Y873F ESCA 3 101371709 101371709 + Missense_Mutation SNP G G T TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr3:101371709G>T c.2383C>A c.(2383-2385)Cag>Aag p.Q795K GBMLGG 3 101370258 101370258 + Missense_Mutation SNP T T G TCGA-QH-A6XC-01A-12D-A32B-08 TCGA-QH-A6XC-10B-01D-A329-08 g.chr3:101370258T>G c.2914A>C c.(2914-2916)Atg>Ctg p.M972L GBMLGG 3 101370464 101370464 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101370464C>T c.2708G>A c.(2707-2709)cGc>cAc p.R903H GBMLGG 3 101373567 101373567 + Nonsense_Mutation SNP G G A TCGA-DB-A64W-01A-11D-A29Q-08 TCGA-DB-A64W-10A-01D-A29Q-08 g.chr3:101373567G>A c.2290C>T c.(2290-2292)Cga>Tga p.R764* GBMLGG 3 101378786 101378786 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101378786C>T c.1887G>A c.(1885-1887)tcG>tcA p.S629S GBMLGG 3 101383381 101383381 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101383381C>A c.e5+1 GBMLGG 3 101383909 101383909 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101383909G>A c.1522C>T c.(1522-1524)Cga>Tga p.R508* GBMLGG 3 101384637 101384637 + Missense_Mutation SNP C C T TCGA-S9-A7R1-01A-12D-A34J-08 TCGA-S9-A7R1-10A-01D-A34M-08 g.chr3:101384637C>T c.794G>A c.(793-795)aGc>aAc p.S265N HNSC 3 101370231 101370231 + Missense_Mutation SNP G G C TCGA-D6-A4ZB-01A-11D-A25D-08 TCGA-D6-A4ZB-10A-01D-A25E-08 g.chr3:101370231G>C c.2941C>G c.(2941-2943)Caa>Gaa p.Q981E HNSC 3 101370392 101370392 + Missense_Mutation SNP C C A TCGA-CR-6487-01A-11D-1870-08 TCGA-CR-6487-10A-01D-1870-08 g.chr3:101370392C>A c.2780G>T c.(2779-2781)cGa>cTa p.R927L HNSC 3 101370490 101370490 + Silent SNP A A G TCGA-MT-A67A-01A-11D-A30E-08 TCGA-MT-A67A-10A-01D-A30H-08 g.chr3:101370490A>G c.2682T>C c.(2680-2682)gcT>gcC p.A894A HNSC 3 101373663 101373663 + Nonsense_Mutation SNP C C A TCGA-CR-5248-01A-01D-2012-08 TCGA-CR-5248-10A-01D-2013-08 g.chr3:101373663C>A c.2194G>T c.(2194-2196)Gag>Tag p.E732* HNSC 3 101375081 101375081 + Missense_Mutation SNP C C G TCGA-CV-6954-01A-11D-1912-08 TCGA-CV-6954-10A-01D-1912-08 g.chr3:101375081C>G c.2058G>C c.(2056-2058)aaG>aaC p.K686N HNSC 3 101383452 101383452 + Missense_Mutation SNP A A T TCGA-UF-A719-01A-12D-A34J-08 TCGA-UF-A719-10A-01D-A34M-08 g.chr3:101383452A>T c.1730T>A c.(1729-1731)gTt>gAt p.V577D HNSC 3 101383838 101383838 + Frame_Shift_Del DEL C C - TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr3:101383838delC c.1593delG c.(1591-1593)cggfs p.R531fs HNSC 3 101390839 101390839 + Nonsense_Mutation SNP T T A TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr3:101390839T>A c.529A>T c.(529-531)Aaa>Taa p.K177* HNSC 3 101395454 101395454 + Nonsense_Mutation SNP C C T TCGA-IQ-A6SH-01A-12D-A34J-08 TCGA-IQ-A6SH-10A-01D-A34M-08 g.chr3:101395454C>T c.305G>A c.(304-306)tGg>tAg p.W102* KICH 3 101395694 101395694 + Missense_Mutation SNP G G A TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr3:101395694G>A c.65C>T c.(64-66)gCg>gTg p.A22V KIPAN 3 101370105 101370105 + Missense_Mutation SNP C C T TCGA-G7-6797-01A-11D-1961-08 TCGA-G7-6797-10A-01D-1962-08 g.chr3:101370105C>T c.3067G>A c.(3067-3069)Gta>Ata p.V1023I KIPAN 3 101370247 101370247 + Missense_Mutation SNP T T G TCGA-B9-4116-01A-01D-1252-08 TCGA-B9-4116-10A-01D-1252-08 g.chr3:101370247T>G c.2925A>C c.(2923-2925)caA>caC p.Q975H KIPAN 3 101371385 101371385 + Missense_Mutation SNP A A C TCGA-UZ-A9PS-01A-11D-A42J-10 TCGA-UZ-A9PS-10A-01D-A42M-10 g.chr3:101371385A>C c.2599T>G c.(2599-2601)Ttc>Gtc p.F867V KIPAN 3 101371390 101371390 + Missense_Mutation SNP C C T TCGA-UZ-A9PS-01A-11D-A42J-10 TCGA-UZ-A9PS-10A-01D-A42M-10 g.chr3:101371390C>T c.2594G>A c.(2593-2595)aGa>aAa p.R865K KIPAN 3 101378652 101378652 + Missense_Mutation SNP G G C TCGA-BQ-5875-01A-11D-1589-08 TCGA-BQ-5875-11A-01D-1589-08 g.chr3:101378652G>C c.2021C>G c.(2020-2022)aCa>aGa p.T674R KIPAN 3 101378747 101378747 + Silent SNP A A T TCGA-BP-5181-01A-01D-1429-08 TCGA-BP-5181-11A-01D-1429-08 g.chr3:101378747A>T c.1926T>A c.(1924-1926)tcT>tcA p.S642S KIPAN 3 101378845 101378846 + Frame_Shift_Del DEL CA CA - TCGA-CJ-4869-01A-02D-1429-08 TCGA-CJ-4869-11A-01D-1429-08 g.chr3:101378845_101378846delCA c.1827_1828delTG c.(1825-1830)agtgccfs p.A610fs KIPAN 3 101390027 101390027 + Missense_Mutation SNP A A G TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr3:101390027A>G c.725T>C c.(724-726)cTt>cCt p.L242P KIPAN 3 101390912 101390912 + Silent SNP C C A TCGA-HE-7129-01A-11D-1961-08 TCGA-HE-7129-10A-01D-1962-08 g.chr3:101390912C>A c.456G>T c.(454-456)tcG>tcT p.S152S KIPAN 3 101395694 101395694 + Missense_Mutation SNP G G A TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr3:101395694G>A c.65C>T c.(64-66)gCg>gTg p.A22V KIRC 3 101378747 101378747 + Silent SNP A A T TCGA-BP-5181-01A-01D-1429-08 TCGA-BP-5181-11A-01D-1429-08 g.chr3:101378747A>T c.1926T>A c.(1924-1926)tcT>tcA p.S642S KIRC 3 101378845 101378846 + Frame_Shift_Del DEL CA CA - TCGA-CJ-4869-01A-02D-1429-08 TCGA-CJ-4869-11A-01D-1429-08 g.chr3:101378845_101378846delCA c.1827_1828delTG c.(1825-1830)agtgccfs p.A610fs KIRP 3 101370105 101370105 + Missense_Mutation SNP C C T TCGA-G7-6797-01A-11D-1961-08 TCGA-G7-6797-10A-01D-1962-08 g.chr3:101370105C>T c.3067G>A c.(3067-3069)Gta>Ata p.V1023I KIRP 3 101370247 101370247 + Missense_Mutation SNP T T G TCGA-B9-4116-01A-01D-1252-08 TCGA-B9-4116-10A-01D-1252-08 g.chr3:101370247T>G c.2925A>C c.(2923-2925)caA>caC p.Q975H KIRP 3 101371385 101371385 + Missense_Mutation SNP A A C TCGA-UZ-A9PS-01A-11D-A42J-10 TCGA-UZ-A9PS-10A-01D-A42M-10 g.chr3:101371385A>C c.2599T>G c.(2599-2601)Ttc>Gtc p.F867V KIRP 3 101371390 101371390 + Missense_Mutation SNP C C T TCGA-UZ-A9PS-01A-11D-A42J-10 TCGA-UZ-A9PS-10A-01D-A42M-10 g.chr3:101371390C>T c.2594G>A c.(2593-2595)aGa>aAa p.R865K KIRP 3 101378652 101378652 + Missense_Mutation SNP G G C TCGA-BQ-5875-01A-11D-1589-08 TCGA-BQ-5875-11A-01D-1589-08 g.chr3:101378652G>C c.2021C>G c.(2020-2022)aCa>aGa p.T674R KIRP 3 101390027 101390027 + Missense_Mutation SNP A A G TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr3:101390027A>G c.725T>C c.(724-726)cTt>cCt p.L242P KIRP 3 101390912 101390912 + Silent SNP C C A TCGA-HE-7129-01A-11D-1961-08 TCGA-HE-7129-10A-01D-1962-08 g.chr3:101390912C>A c.456G>T c.(454-456)tcG>tcT p.S152S LGG 3 101370258 101370258 + Missense_Mutation SNP T T G TCGA-QH-A6XC-01A-12D-A32B-08 TCGA-QH-A6XC-10B-01D-A329-08 g.chr3:101370258T>G c.2914A>C c.(2914-2916)Atg>Ctg p.M972L LGG 3 101370464 101370464 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101370464C>T c.2708G>A c.(2707-2709)cGc>cAc p.R903H LGG 3 101373567 101373567 + Nonsense_Mutation SNP G G A TCGA-DB-A64W-01A-11D-A29Q-08 TCGA-DB-A64W-10A-01D-A29Q-08 g.chr3:101373567G>A c.2290C>T c.(2290-2292)Cga>Tga p.R764* LGG 3 101378786 101378786 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101378786C>T c.1887G>A c.(1885-1887)tcG>tcA p.S629S LGG 3 101383381 101383381 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101383381C>A c.e5+1 LGG 3 101383909 101383909 + Nonsense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:101383909G>A c.1522C>T c.(1522-1524)Cga>Tga p.R508* LGG 3 101384637 101384637 + Missense_Mutation SNP C C T TCGA-S9-A7R1-01A-12D-A34J-08 TCGA-S9-A7R1-10A-01D-A34M-08 g.chr3:101384637C>T c.794G>A c.(793-795)aGc>aAc p.S265N LIHC 3 101370476 101370476 + Missense_Mutation SNP C C A TCGA-NI-A8LF-01A-11D-A35Z-10 TCGA-NI-A8LF-10A-01D-A35Z-10 g.chr3:101370476C>A c.2696G>T c.(2695-2697)cGa>cTa p.R899L LIHC 3 101371772 101371772 + Frame_Shift_Del DEL T T - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr3:101371772delT c.2320delA c.(2320-2322)agtfs p.S774fs LIHC 3 101383437 101383437 + Missense_Mutation SNP T T C TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr3:101383437T>C c.1745A>G c.(1744-1746)tAc>tGc p.Y582C LIHC 3 101383939 101383939 + Missense_Mutation SNP G G A TCGA-DD-A4NJ-01A-11D-A27I-10 TCGA-DD-A4NJ-10A-01D-A27I-10 g.chr3:101383939G>A c.1492C>T c.(1492-1494)Cct>Tct p.P498S LUAD 3 101370066 101370066 + Missense_Mutation SNP C C A TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr3:101370066C>A c.3106G>T c.(3106-3108)Gca>Tca p.A1036S LUAD 3 101370100 101370100 + Missense_Mutation SNP T T A TCGA-64-5775-01A-01D-1625-08 TCGA-64-5775-10A-01D-1625-08 g.chr3:101370100T>A c.3072A>T c.(3070-3072)ttA>ttT p.L1024F LUAD 3 101384009 101384009 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr3:101384009C>A c.1422G>T c.(1420-1422)agG>agT p.R474S LUAD 3 101384010 101384010 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr3:101384010C>A c.1421G>T c.(1420-1422)aGg>aTg p.R474M LUAD 3 101390835 101390835 + Missense_Mutation SNP T T C TCGA-55-7724-01A-11D-2167-08 TCGA-55-7724-10A-01D-2167-08 g.chr3:101390835T>C c.533A>G c.(532-534)cAt>cGt p.H178R LUAD 3 101390880 101390880 + Missense_Mutation SNP G G A TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr3:101390880G>A c.488C>T c.(487-489)cCa>cTa p.P163L LUAD 3 101390998 101390998 + Missense_Mutation SNP C C G TCGA-78-7146-01A-11D-2036-08 TCGA-78-7146-10A-01D-2036-08 g.chr3:101390998C>G c.370G>C c.(370-372)Gat>Cat p.D124H LUSC 3 101370029 101370029 + Missense_Mutation SNP T T C TCGA-63-5128-01A-01D-1441-08 TCGA-63-5128-10A-01D-1441-08 g.chr3:101370029T>C c.3143A>G c.(3142-3144)cAt>cGt p.H1048R LUSC 3 101375038 101375038 + Missense_Mutation SNP G G A TCGA-21-5782-01A-01D-1632-08 TCGA-21-5782-10A-01D-1632-08 g.chr3:101375038G>A c.2101C>T c.(2101-2103)Cat>Tat p.H701Y LUSC 3 101383876 101383876 + Nonsense_Mutation SNP G G A TCGA-66-2765-01A-01D-1522-08 TCGA-66-2765-11A-01D-1522-08 g.chr3:101383876G>A c.1555C>T c.(1555-1557)Cga>Tga p.R519* LUSC 3 101384599 101384599 + Silent SNP G G A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr3:101384599G>A c.832C>T c.(832-834)Cta>Tta p.L278L LUSC 3 101390001 101390001 + Missense_Mutation SNP T T A TCGA-22-4604-01A-01D-1267-08 TCGA-22-4604-11A-01D-1267-08 g.chr3:101390001T>A c.751A>T c.(751-753)Agt>Tgt p.S251C LUSC 3 101390091 101390091 + Missense_Mutation SNP C C T TCGA-85-6175-01A-11D-1817-08 TCGA-85-6175-10A-01D-1817-08 g.chr3:101390091C>T c.661G>A c.(661-663)Gaa>Aaa p.E221K OV 3 101370048 101370048 + Missense_Mutation SNP C C G TCGA-29-1763-01A-02W-0633-09 TCGA-29-1763-10A-01W-0633-09 g.chr3:101370048C>G c.3124G>C c.(3124-3126)Gtt>Ctt p.V1042L OV 3 101370393 101370393 + Nonsense_Mutation SNP G G A TCGA-25-1635-01A-01W-0615-10 TCGA-25-1635-10A-01W-0616-10 g.chr3:101370393G>A c.2779C>T c.(2779-2781)Cga>Tga p.R927* PAAD 3 101373562 101373562 + Silent SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:101373562G>T c.2295C>A c.(2293-2295)ggC>ggA p.G765G PAAD 3 101383834 101383834 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:101383834C>T c.1597G>A c.(1597-1599)Gcc>Acc p.A533T PRAD 3 101383903 101383903 + Missense_Mutation SNP G G A TCGA-HC-7231-01A-11D-2114-08 TCGA-HC-7231-10A-01D-2115-08 g.chr3:101383903G>A c.1528C>T c.(1528-1530)Cgt>Tgt p.R510C PRAD 3 101384241 101384241 + Nonsense_Mutation SNP G G C TCGA-G9-6329-01A-13D-1961-08 TCGA-G9-6329-10A-01D-1961-08 g.chr3:101384241G>C c.1190C>G c.(1189-1191)tCa>tGa p.S397* READ 3 101370201 101370201 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:101370201C>A c.2971G>T c.(2971-2973)Gaa>Taa p.E991* READ 3 101373592 101373592 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:101373592C>A c.2265G>T c.(2263-2265)aaG>aaT p.K755N READ 3 101374975 101374975 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:101374975G>T c.2164C>A c.(2164-2166)Ctt>Att p.L722I SARC 3 101375072 101375072 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr3:101375072G>A c.2067C>T c.(2065-2067)atC>atT p.I689I SKCM 3 101370483 101370483 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr3:101370483C>T c.2689G>A c.(2689-2691)Gat>Aat p.D897N SKCM 3 101378854 101378854 + Nonsense_Mutation SNP G G A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr3:101378854G>A c.1819C>T c.(1819-1821)Cag>Tag p.Q607* SKCM 3 101383815 101383815 + Missense_Mutation SNP A A G TCGA-EE-A2GS-06A-12D-A197-08 TCGA-EE-A2GS-10A-01D-A199-08 g.chr3:101383815A>G c.1616T>C c.(1615-1617)gTt>gCt p.V539A SKCM 3 101384430 101384430 + Missense_Mutation SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr3:101384430C>T c.1001G>A c.(1000-1002)cGa>cAa p.R334Q SKCM 3 101384585 101384585 + Missense_Mutation SNP G G T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr3:101384585G>T c.846C>A c.(844-846)ttC>ttA p.F282L SKCM 3 101390172 101390172 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:101390172G>A c.580C>T c.(580-582)Cca>Tca p.P194S SKCM 3 101395684 101395684 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr3:101395684G>A c.75C>T c.(73-75)acC>acT p.T25T

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 3 101390938 101390938 single base substitution C T missense_variant E144K 430G>A BLCA-US 3 101370486 101370486 single base substitution C T downstream_gene_variant BLCA-US 3 101370486 101370486 single base substitution C T missense_variant A896T 2686G>A BLCA-US 3 101378715 101378715 single base substitution C T exon_variant BLCA-US 3 101378715 101378715 single base substitution C T missense_variant C653Y 1958G>A BLCA-US 3 101390113 101390113 single base substitution G A 3_prime_UTR_variant BLCA-US 3 101390113 101390113 single base substitution G A synonymous_variant F213F 639C>T BLCA-US 3 101399989 101399989 single base substitution C T upstream_gene_variant BLCA-US 3 101400024 101400024 single base substitution C A upstream_gene_variant BRCA-EU 3 101362775 101362775 single base substitution G T downstream_gene_variant BRCA-EU 3 101363232 101363232 single base substitution C A downstream_gene_variant BRCA-EU 3 101363760 101363760 single base substitution G A downstream_gene_variant BRCA-EU 3 101363876 101363876 single base substitution G C downstream_gene_variant BRCA-EU 3 101365529 101365529 single base substitution C T downstream_gene_variant BRCA-EU 3 101366613 101366613 single base substitution C G downstream_gene_variant BRCA-EU 3 101366823 101366823 single base substitution G A downstream_gene_variant BRCA-EU 3 101366914 101366914 single base substitution C G downstream_gene_variant BRCA-EU 3 101367231 101367231 single base substitution C T downstream_gene_variant BRCA-EU 3 101371767 101371767 single base substitution G C downstream_gene_variant BRCA-EU 3 101371767 101371767 single base substitution G C missense_variant F775L 2325C>G BRCA-EU 3 101372902 101372902 single base substitution G A downstream_gene_variant BRCA-EU 3 101372902 101372902 single base substitution G A intron_variant BRCA-EU 3 101373483 101373483 insertion of <=200bp - T downstream_gene_variant BRCA-EU 3 101373483 101373483 insertion of <=200bp - T intron_variant BRCA-EU 3 101373735 101373735 single base substitution T C downstream_gene_variant BRCA-EU 3 101373735 101373735 single base substitution T C intron_variant BRCA-EU 3 101374876 101374876 single base substitution T C exon_variant BRCA-EU 3 101374876 101374876 single base substitution T C intron_variant BRCA-EU 3 101375487 101375487 deletion of <=200bp T - intron_variant BRCA-EU 3 101375699 101375699 single base substitution C T intron_variant BRCA-EU 3 101375762 101375762 single base substitution G A intron_variant BRCA-EU 3 101378094 101378094 deletion of <=200bp A - intron_variant BRCA-EU 3 101381089 101381089 single base substitution G C intron_variant BRCA-EU 3 101381089 101381089 single base substitution G C upstream_gene_variant BRCA-EU 3 101387317 101387317 single base substitution G A downstream_gene_variant BRCA-EU 3 101387317 101387317 single base substitution G A intron_variant BRCA-EU 3 101391050 101391050 single base substitution C T synonymous_variant L106L 318G>A BRCA-EU 3 101391261 101391261 insertion of <=200bp - T intron_variant BRCA-EU 3 101391698 101391698 single base substitution A C intron_variant BRCA-EU 3 101393376 101393376 single base substitution G T intron_variant BRCA-EU 3 101394191 101394191 single base substitution G A intron_variant BRCA-EU 3 101394846 101394846 deletion of <=200bp A - intron_variant BRCA-EU 3 101396268 101396268 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 3 101396268 101396268 single base substitution G A upstream_gene_variant BRCA-EU 3 101397687 101397687 deletion of <=200bp A - upstream_gene_variant BRCA-EU 3 101399343 101399343 deletion of <=200bp A - upstream_gene_variant BRCA-EU 3 101399819 101399819 single base substitution C T upstream_gene_variant BRCA-EU 3 101400820 101400820 single base substitution G T upstream_gene_variant BRCA-EU 3 101401139 101401139 single base substitution G A upstream_gene_variant BRCA-FR 3 101365529 101365529 single base substitution C T downstream_gene_variant BRCA-FR 3 101366557 101366557 single base substitution G A downstream_gene_variant BRCA-FR 3 101366823 101366823 single base substitution G A downstream_gene_variant BRCA-FR 3 101371767 101371767 single base substitution G C downstream_gene_variant BRCA-FR 3 101371767 101371767 single base substitution G C missense_variant F775L 2325C>G BRCA-FR 3 101372902 101372902 single base substitution G A downstream_gene_variant BRCA-FR 3 101372902 101372902 single base substitution G A intron_variant BRCA-FR 3 101381974 101381974 single base substitution G A intron_variant BRCA-FR 3 101381974 101381974 single base substitution G A upstream_gene_variant BRCA-UK 3 101363760 101363760 single base substitution G A downstream_gene_variant BRCA-UK 3 101392543 101392543 single base substitution G C intron_variant BRCA-US 3 101370304 101370304 single base substitution G A downstream_gene_variant BRCA-US 3 101370304 101370304 single base substitution G A synonymous_variant N956N 2868C>T BRCA-US 3 101370349 101370349 single base substitution C T downstream_gene_variant BRCA-US 3 101370349 101370349 single base substitution C T synonymous_variant V941V 2823G>A BRCA-US 3 101370392 101370392 single base substitution C T downstream_gene_variant BRCA-US 3 101370392 101370392 single base substitution C T missense_variant R927Q 2780G>A BRCA-US 3 101375072 101375072 single base substitution G C exon_variant BRCA-US 3 101375072 101375072 single base substitution G C missense_variant I689M 2067C>G BRCA-US 3 101378855 101378855 single base substitution A C missense_variant F606L 1818T>G BRCA-US 3 101378855 101378855 single base substitution A C upstream_gene_variant BRCA-US 3 101390741 101390741 insertion of <=200bp - G frameshift_variant Q209Q? BRCA-US 3 101390741 101390741 insertion of <=200bp - G intron_variant BTCA-JP 3 101378642 101378642 deletion of <=200bp C - exon_variant BTCA-JP 3 101378642 101378642 deletion of <=200bp C - frameshift_variant K677 BTCA-JP 3 101395549 101395549 single base substitution T G synonymous_variant R70R 210A>C CESC-US 3 101374961 101374961 single base substitution C G exon_variant CESC-US 3 101374961 101374961 single base substitution C G missense_variant M726I 2178G>C CESC-US 3 101383876 101383876 single base substitution G A stop_gained R519* 1555C>T CESC-US 3 101384145 101384145 single base substitution C G missense_variant R429T 1286G>C CESC-US 3 101390764 101390764 single base substitution C G intron_variant CESC-US 3 101390764 101390764 single base substitution C G missense_variant A202P 604G>C CLLE-ES 3 101365296 101365296 single base substitution G A downstream_gene_variant CLLE-ES 3 101374491 101374491 single base substitution C A downstream_gene_variant CLLE-ES 3 101374491 101374491 single base substitution C A intron_variant CLLE-ES 3 101385369 101385369 single base substitution T C downstream_gene_variant CLLE-ES 3 101385369 101385369 single base substitution T C intron_variant COAD-US 3 101370080 101370080 single base substitution T G downstream_gene_variant COAD-US 3 101370080 101370080 single base substitution T G missense_variant K1031T 3092A>C COAD-US 3 101370530 101370533 deletion of <=200bp AAAA - downstream_gene_variant COAD-US 3 101370530 101370533 deletion of <=200bp AAAA - intron_variant COAD-US 3 101378774 101378774 single base substitution C T synonymous_variant T633T 1899G>A COAD-US 3 101378774 101378774 single base substitution C T upstream_gene_variant COAD-US 3 101384048 101384048 single base substitution T C synonymous_variant S461S 1383A>G COAD-US 3 101384352 101384352 single base substitution T C missense_variant D360G 1079A>G COAD-US 3 101384465 101384465 single base substitution G A downstream_gene_variant COAD-US 3 101384465 101384465 single base substitution G A synonymous_variant G322G 966C>T COAD-US 3 101399983 101399983 single base substitution C T upstream_gene_variant COCA-CN 3 101370163 101370163 single base substitution T C downstream_gene_variant COCA-CN 3 101370163 101370163 single base substitution T C synonymous_variant E1003E 3009A>G COCA-CN 3 101371387 101371387 single base substitution T G downstream_gene_variant COCA-CN 3 101371387 101371387 single base substitution T G missense_variant K866T 2597A>C COCA-CN 3 101374899 101374899 single base substitution C A exon_variant COCA-CN 3 101374899 101374899 single base substitution C A intron_variant COCA-CN 3 101384099 101384099 single base substitution C A missense_variant E444D 1332G>T COCA-CN 3 101384227 101384227 single base substitution T C missense_variant I402V 1204A>G COCA-CN 3 101384323 101384323 single base substitution C A stop_gained E370* 1108G>T COCA-CN 3 101390033 101390033 single base substitution C T 3_prime_UTR_variant COCA-CN 3 101390033 101390033 single base substitution C T missense_variant R240Q 719G>A COCA-CN 3 101390852 101390852 single base substitution C A missense_variant K172N 516G>T COCA-CN 3 101390994 101390994 single base substitution C T missense_variant R125Q 374G>A ESAD-UK 3 101364012 101364012 single base substitution G A downstream_gene_variant ESAD-UK 3 101365217 101365217 single base substitution T C downstream_gene_variant ESAD-UK 3 101366809 101366809 single base substitution C A downstream_gene_variant ESAD-UK 3 101367935 101367935 single base substitution C A 3_prime_UTR_variant ESAD-UK 3 101371096 101371096 single base substitution A G downstream_gene_variant ESAD-UK 3 101371096 101371096 single base substitution A G intron_variant ESAD-UK 3 101371356 101371356 single base substitution G A downstream_gene_variant ESAD-UK 3 101371356 101371356 single base substitution G A synonymous_variant H876H 2628C>T ESAD-UK 3 101371956 101371956 single base substitution C G downstream_gene_variant ESAD-UK 3 101371956 101371956 single base substitution C G intron_variant ESAD-UK 3 101374544 101374544 single base substitution G A downstream_gene_variant ESAD-UK 3 101374544 101374544 single base substitution G A intron_variant ESAD-UK 3 101374702 101374702 single base substitution C T exon_variant ESAD-UK 3 101374702 101374702 single base substitution C T intron_variant ESAD-UK 3 101374843 101374843 single base substitution G A exon_variant ESAD-UK 3 101374843 101374843 single base substitution G A intron_variant ESAD-UK 3 101377785 101377785 single base substitution T G intron_variant ESAD-UK 3 101379363 101379363 single base substitution C G intron_variant ESAD-UK 3 101379363 101379363 single base substitution C G upstream_gene_variant ESAD-UK 3 101381026 101381026 single base substitution T A intron_variant ESAD-UK 3 101381026 101381026 single base substitution T A upstream_gene_variant ESAD-UK 3 101382097 101382097 single base substitution G A intron_variant ESAD-UK 3 101382097 101382097 single base substitution G A upstream_gene_variant ESAD-UK 3 101383819 101383819 single base substitution C T missense_variant A538T 1612G>A ESAD-UK 3 101385613 101385613 single base substitution G T downstream_gene_variant ESAD-UK 3 101385613 101385613 single base substitution G T intron_variant ESAD-UK 3 101387293 101387293 single base substitution G T downstream_gene_variant ESAD-UK 3 101387293 101387293 single base substitution G T intron_variant ESAD-UK 3 101393143 101393143 single base substitution G A intron_variant ESAD-UK 3 101393949 101393949 single base substitution T C intron_variant ESAD-UK 3 101394942 101394942 single base substitution G A intron_variant ESAD-UK 3 101396701 101396701 single base substitution A G upstream_gene_variant ESAD-UK 3 101400907 101400907 single base substitution A G upstream_gene_variant ESAD-UK 3 101401103 101401103 single base substitution G A upstream_gene_variant ESCA-CN 3 101370529 101370529 single base substitution T A downstream_gene_variant ESCA-CN 3 101370529 101370529 single base substitution T A splice_acceptor_variant ESCA-CN 3 101390090 101390090 single base substitution T A 3_prime_UTR_variant ESCA-CN 3 101390090 101390090 single base substitution T A missense_variant E221V 662A>T KIRP-US 3 101370105 101370105 single base substitution C T downstream_gene_variant KIRP-US 3 101370105 101370105 single base substitution C T missense_variant V1023I 3067G>A KIRP-US 3 101378652 101378652 single base substitution G C exon_variant KIRP-US 3 101378652 101378652 single base substitution G C missense_variant T674R 2021C>G KIRP-US 3 101390027 101390027 single base substitution A G 3_prime_UTR_variant KIRP-US 3 101390027 101390027 single base substitution A G missense_variant L242P 725T>C LAML-KR 3 101373781 101373781 single base substitution G T downstream_gene_variant LAML-KR 3 101373781 101373781 single base substitution G T intron_variant LAML-KR 3 101399883 101399883 single base substitution G A upstream_gene_variant LGG-US 3 101373567 101373567 single base substitution G A downstream_gene_variant LGG-US 3 101373567 101373567 single base substitution G A stop_gained R764* 2290C>T LICA-CN 3 101375085 101375085 single base substitution C T exon_variant LICA-CN 3 101375085 101375085 single base substitution C T missense_variant G685E 2054G>A LICA-FR 3 101363987 101363987 deletion of <=200bp T - downstream_gene_variant LICA-FR 3 101370530 101370531 deletion of <=200bp AA - downstream_gene_variant LICA-FR 3 101370530 101370531 deletion of <=200bp AA - intron_variant LICA-FR 3 101372475 101372475 single base substitution T C downstream_gene_variant LICA-FR 3 101372475 101372475 single base substitution T C intron_variant LICA-FR 3 101372888 101372888 insertion of <=200bp - T downstream_gene_variant LICA-FR 3 101372888 101372888 insertion of <=200bp - T intron_variant LICA-FR 3 101390183 101390183 single base substitution T G 3_prime_UTR_variant LICA-FR 3 101390183 101390183 single base substitution T G missense_variant K190T 569A>C LICA-FR 3 101395559 101395559 single base substitution T G missense_variant Q67P 200A>C LICA-FR 3 101400045 101400045 single base substitution T C upstream_gene_variant LIHC-US 3 101383939 101383939 single base substitution G A missense_variant P498S 1492C>T LINC-JP 3 101373727 101373727 single base substitution T C downstream_gene_variant LINC-JP 3 101373727 101373727 single base substitution T C intron_variant LINC-JP 3 101383468 101383479 deletion of <=200bp CACATTTATGAG - disruptive_inframe_deletion SHKCG568W LINC-JP 3 101383468 101383479 deletion of <=200bp CACATTTATGAG - upstream_gene_variant LINC-JP 3 101383570 101383570 single base substitution T A intron_variant LINC-JP 3 101383570 101383570 single base substitution T A upstream_gene_variant LINC-JP 3 101384492 101384492 single base substitution C G downstream_gene_variant LINC-JP 3 101384492 101384492 single base substitution C G missense_variant E313D 939G>C LINC-JP 3 101392879 101392880 deletion of <=200bp TT - intron_variant LINC-JP 3 101395965 101395965 single base substitution C T 5_prime_UTR_variant LINC-JP 3 101395965 101395965 single base substitution C T upstream_gene_variant LIRI-JP 3 101365477 101365477 single base substitution T C downstream_gene_variant LIRI-JP 3 101365568 101365568 single base substitution T C downstream_gene_variant LIRI-JP 3 101365726 101365726 single base substitution T C downstream_gene_variant LIRI-JP 3 101365745 101365745 single base substitution T C downstream_gene_variant LIRI-JP 3 101369129 101369129 single base substitution C A 3_prime_UTR_variant LIRI-JP 3 101370131 101370131 single base substitution T C downstream_gene_variant LIRI-JP 3 101370131 101370131 single base substitution T C missense_variant Q1014R 3041A>G LIRI-JP 3 101372251 101372251 single base substitution C A downstream_gene_variant LIRI-JP 3 101372251 101372251 single base substitution C A intron_variant LIRI-JP 3 101372438 101372438 single base substitution T C downstream_gene_variant LIRI-JP 3 101372438 101372438 single base substitution T C intron_variant LIRI-JP 3 101372631 101372631 single base substitution G A downstream_gene_variant LIRI-JP 3 101372631 101372631 single base substitution G A intron_variant LIRI-JP 3 101374673 101374673 single base substitution G A downstream_gene_variant LIRI-JP 3 101374673 101374673 single base substitution G A intron_variant LIRI-JP 3 101374741 101374741 single base substitution T A exon_variant LIRI-JP 3 101374741 101374741 single base substitution T A intron_variant LIRI-JP 3 101377407 101377407 single base substitution G C intron_variant LIRI-JP 3 101380525 101380525 single base substitution T C intron_variant LIRI-JP 3 101380525 101380525 single base substitution T C upstream_gene_variant LIRI-JP 3 101380867 101380867 single base substitution C T intron_variant LIRI-JP 3 101380867 101380867 single base substitution C T upstream_gene_variant LIRI-JP 3 101382919 101382919 single base substitution G A intron_variant LIRI-JP 3 101382919 101382919 single base substitution G A upstream_gene_variant LIRI-JP 3 101386624 101386624 single base substitution T C downstream_gene_variant LIRI-JP 3 101386624 101386624 single base substitution T C intron_variant LIRI-JP 3 101387117 101387117 single base substitution G T downstream_gene_variant LIRI-JP 3 101387117 101387117 single base substitution G T intron_variant LIRI-JP 3 101387577 101387577 single base substitution T C downstream_gene_variant LIRI-JP 3 101387577 101387577 single base substitution T C intron_variant LIRI-JP 3 101387969 101387969 single base substitution T C downstream_gene_variant LIRI-JP 3 101387969 101387969 single base substitution T C intron_variant LIRI-JP 3 101388256 101388256 single base substitution T C downstream_gene_variant LIRI-JP 3 101388256 101388256 single base substitution T C intron_variant LIRI-JP 3 101389144 101389144 single base substitution T C downstream_gene_variant LIRI-JP 3 101389144 101389144 single base substitution T C intron_variant LIRI-JP 3 101389665 101389665 single base substitution A T 3_prime_UTR_variant LIRI-JP 3 101389665 101389665 single base substitution A T intron_variant LIRI-JP 3 101389835 101389835 single base substitution C T 3_prime_UTR_variant LIRI-JP 3 101389835 101389835 single base substitution C T intron_variant LIRI-JP 3 101389933 101389933 single base substitution G T 3_prime_UTR_variant LIRI-JP 3 101389933 101389933 single base substitution G T intron_variant LIRI-JP 3 101391942 101391942 single base substitution T C intron_variant LIRI-JP 3 101392276 101392276 insertion of <=200bp - C intron_variant LIRI-JP 3 101393152 101393152 single base substitution T C intron_variant LIRI-JP 3 101393241 101393241 single base substitution G C intron_variant LIRI-JP 3 101394226 101394226 single base substitution C T intron_variant LIRI-JP 3 101395427 101395427 single base substitution C G intron_variant LIRI-JP 3 101397961 101397961 single base substitution C T upstream_gene_variant LIRI-JP 3 101399002 101399002 single base substitution A T upstream_gene_variant LIRI-JP 3 101400270 101400270 single base substitution A C upstream_gene_variant LUSC-KR 3 101363290 101363290 single base substitution C G downstream_gene_variant LUSC-KR 3 101363722 101363722 single base substitution C A downstream_gene_variant LUSC-KR 3 101365106 101365106 single base substitution C T downstream_gene_variant LUSC-KR 3 101371382 101371382 single base substitution T A downstream_gene_variant LUSC-KR 3 101371382 101371382 single base substitution T A missense_variant T868S 2602A>T LUSC-KR 3 101384558 101384558 single base substitution T G downstream_gene_variant LUSC-KR 3 101384558 101384558 single base substitution T G missense_variant L291F 873A>C LUSC-KR 3 101387015 101387015 single base substitution G T downstream_gene_variant LUSC-KR 3 101387015 101387015 single base substitution G T intron_variant LUSC-KR 3 101390208 101390208 single base substitution G T 3_prime_UTR_variant LUSC-KR 3 101390208 101390208 single base substitution G T splice_region_variant LUSC-US 3 101370029 101370029 single base substitution T C downstream_gene_variant LUSC-US 3 101370029 101370029 single base substitution T C missense_variant H1048R 3143A>G LUSC-US 3 101375038 101375038 single base substitution G A exon_variant LUSC-US 3 101375038 101375038 single base substitution G A missense_variant H701Y 2101C>T LUSC-US 3 101383876 101383876 single base substitution G A stop_gained R519* 1555C>T LUSC-US 3 101384599 101384599 single base substitution G A downstream_gene_variant LUSC-US 3 101384599 101384599 single base substitution G A synonymous_variant L278L 832C>T LUSC-US 3 101390001 101390001 single base substitution T A 3_prime_UTR_variant LUSC-US 3 101390001 101390001 single base substitution T A missense_variant S251C 751A>T LUSC-US 3 101390091 101390091 single base substitution C T 3_prime_UTR_variant LUSC-US 3 101390091 101390091 single base substitution C T missense_variant E221K 661G>A MALY-DE 3 101371893 101371893 single base substitution T G downstream_gene_variant MALY-DE 3 101371893 101371893 single base substitution T G intron_variant MALY-DE 3 101372161 101372161 single base substitution A T downstream_gene_variant MALY-DE 3 101372161 101372161 single base substitution A T intron_variant MALY-DE 3 101381174 101381174 deletion of <=200bp A - intron_variant MALY-DE 3 101381174 101381174 deletion of <=200bp A - upstream_gene_variant MALY-DE 3 101381816 101381816 single base substitution C A intron_variant MALY-DE 3 101381816 101381816 single base substitution C A upstream_gene_variant MALY-DE 3 101396531 101396531 single base substitution T C upstream_gene_variant MELA-AU 3 101362944 101362944 single base substitution G A downstream_gene_variant MELA-AU 3 101363551 101363551 single base substitution G T downstream_gene_variant MELA-AU 3 101363722 101363722 single base substitution C T downstream_gene_variant MELA-AU 3 101364379 101364379 single base substitution G A downstream_gene_variant MELA-AU 3 101364578 101364578 single base substitution G A downstream_gene_variant MELA-AU 3 101365234 101365234 single base substitution G A downstream_gene_variant MELA-AU 3 101365314 101365314 single base substitution G A downstream_gene_variant MELA-AU 3 101366710 101366710 single base substitution G A downstream_gene_variant MELA-AU 3 101366729 101366729 single base substitution G A downstream_gene_variant MELA-AU 3 101367831 101367831 single base substitution G A 3_prime_UTR_variant MELA-AU 3 101367924 101367924 single base substitution C T 3_prime_UTR_variant MELA-AU 3 101367976 101367976 single base substitution G A 3_prime_UTR_variant MELA-AU 3 101368877 101368877 single base substitution G A 3_prime_UTR_variant MELA-AU 3 101368900 101368900 single base substitution T C 3_prime_UTR_variant MELA-AU 3 101370736 101370736 single base substitution G A downstream_gene_variant MELA-AU 3 101370736 101370736 single base substitution G A intron_variant MELA-AU 3 101370870 101370870 single base substitution G A downstream_gene_variant MELA-AU 3 101370870 101370870 single base substitution G A intron_variant MELA-AU 3 101371212 101371212 single base substitution C T downstream_gene_variant MELA-AU 3 101371212 101371212 single base substitution C T intron_variant MELA-AU 3 101372018 101372018 single base substitution G A downstream_gene_variant MELA-AU 3 101372018 101372018 single base substitution G A intron_variant MELA-AU 3 101372840 101372840 single base substitution G A downstream_gene_variant MELA-AU 3 101372840 101372840 single base substitution G A intron_variant MELA-AU 3 101372870 101372870 single base substitution C T downstream_gene_variant MELA-AU 3 101372870 101372870 single base substitution C T intron_variant MELA-AU 3 101373227 101373227 single base substitution G A downstream_gene_variant MELA-AU 3 101373227 101373227 single base substitution G A intron_variant MELA-AU 3 101373390 101373390 single base substitution G A downstream_gene_variant MELA-AU 3 101373390 101373390 single base substitution G A intron_variant MELA-AU 3 101374206 101374206 single base substitution G A downstream_gene_variant MELA-AU 3 101374206 101374206 single base substitution G A intron_variant MELA-AU 3 101374721 101374721 single base substitution G A exon_variant MELA-AU 3 101374721 101374721 single base substitution G A intron_variant MELA-AU 3 101375107 101375107 single base substitution G A intron_variant MELA-AU 3 101375133 101375133 single base substitution G A intron_variant MELA-AU 3 101375770 101375770 single base substitution G A intron_variant MELA-AU 3 101376394 101376394 single base substitution G A intron_variant MELA-AU 3 101376444 101376444 single base substitution G A intron_variant MELA-AU 3 101377096 101377096 single base substitution G A intron_variant MELA-AU 3 101377436 101377436 single base substitution C T intron_variant MELA-AU 3 101377595 101377595 single base substitution G A intron_variant MELA-AU 3 101377949 101377949 single base substitution G A intron_variant MELA-AU 3 101378117 101378117 single base substitution C T intron_variant MELA-AU 3 101378329 101378330 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 3 101378427 101378427 single base substitution G A intron_variant MELA-AU 3 101379277 101379277 single base substitution A G intron_variant MELA-AU 3 101379277 101379277 single base substitution A G upstream_gene_variant MELA-AU 3 101379741 101379741 single base substitution G A intron_variant MELA-AU 3 101379741 101379741 single base substitution G A upstream_gene_variant MELA-AU 3 101380189 101380189 single base substitution G A intron_variant MELA-AU 3 101380189 101380189 single base substitution G A upstream_gene_variant MELA-AU 3 101380822 101380822 single base substitution G A intron_variant MELA-AU 3 101380822 101380822 single base substitution G A upstream_gene_variant MELA-AU 3 101381975 101381975 single base substitution G A intron_variant MELA-AU 3 101381975 101381975 single base substitution G A upstream_gene_variant MELA-AU 3 101382554 101382554 single base substitution G A intron_variant MELA-AU 3 101382554 101382554 single base substitution G A upstream_gene_variant MELA-AU 3 101382560 101382560 single base substitution C A intron_variant MELA-AU 3 101382560 101382560 single base substitution C A upstream_gene_variant MELA-AU 3 101383863 101383863 single base substitution C T missense_variant G523E 1568G>A MELA-AU 3 101384933 101384934 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 3 101384933 101384934 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 101385017 101385017 single base substitution C T downstream_gene_variant MELA-AU 3 101385017 101385017 single base substitution C T intron_variant MELA-AU 3 101385303 101385303 single base substitution G A downstream_gene_variant MELA-AU 3 101385303 101385303 single base substitution G A intron_variant MELA-AU 3 101385397 101385397 single base substitution G A downstream_gene_variant MELA-AU 3 101385397 101385397 single base substitution G A intron_variant MELA-AU 3 101386073 101386073 single base substitution G A downstream_gene_variant MELA-AU 3 101386073 101386073 single base substitution G A intron_variant MELA-AU 3 101386473 101386473 single base substitution G A downstream_gene_variant MELA-AU 3 101386473 101386473 single base substitution G A intron_variant MELA-AU 3 101386528 101386528 single base substitution G A downstream_gene_variant MELA-AU 3 101386528 101386528 single base substitution G A intron_variant MELA-AU 3 101386891 101386891 single base substitution A C downstream_gene_variant MELA-AU 3 101386891 101386891 single base substitution A C intron_variant MELA-AU 3 101388098 101388098 single base substitution G A downstream_gene_variant MELA-AU 3 101388098 101388098 single base substitution G A intron_variant MELA-AU 3 101388140 101388140 single base substitution G A downstream_gene_variant MELA-AU 3 101388140 101388140 single base substitution G A intron_variant MELA-AU 3 101388604 101388604 single base substitution G A downstream_gene_variant MELA-AU 3 101388604 101388604 single base substitution G A intron_variant MELA-AU 3 101388808 101388808 single base substitution G A downstream_gene_variant MELA-AU 3 101388808 101388808 single base substitution G A intron_variant MELA-AU 3 101389127 101389127 single base substitution G A downstream_gene_variant MELA-AU 3 101389127 101389127 single base substitution G A intron_variant MELA-AU 3 101389648 101389648 single base substitution C T 3_prime_UTR_variant MELA-AU 3 101389648 101389648 single base substitution C T intron_variant MELA-AU 3 101390122 101390122 single base substitution G A 3_prime_UTR_variant MELA-AU 3 101390122 101390122 single base substitution G A synonymous_variant S210S 630C>T MELA-AU 3 101392098 101392098 single base substitution G A intron_variant MELA-AU 3 101392107 101392107 single base substitution G A intron_variant MELA-AU 3 101392114 101392114 single base substitution G A intron_variant MELA-AU 3 101392492 101392492 single base substitution G A intron_variant MELA-AU 3 101393181 101393181 single base substitution G A intron_variant MELA-AU 3 101393539 101393539 single base substitution T C intron_variant MELA-AU 3 101393825 101393825 single base substitution G A intron_variant MELA-AU 3 101395134 101395134 single base substitution C T intron_variant MELA-AU 3 101395267 101395268 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 101397466 101397466 single base substitution G A upstream_gene_variant MELA-AU 3 101399002 101399002 single base substitution A G upstream_gene_variant MELA-AU 3 101400252 101400252 single base substitution G T upstream_gene_variant ORCA-IN 3 101390023 101390023 single base substitution A G 3_prime_UTR_variant ORCA-IN 3 101390023 101390023 single base substitution A G synonymous_variant F243F 729T>C ORCA-IN 3 101395488 101395488 single base substitution G C missense_variant Q91E 271C>G ORCA-IN 3 101396732 101396732 single base substitution G A upstream_gene_variant OV-AU 3 101367779 101367779 single base substitution A G 3_prime_UTR_variant OV-AU 3 101373791 101373791 single base substitution G C downstream_gene_variant OV-AU 3 101373791 101373791 single base substitution G C intron_variant OV-AU 3 101375269 101375269 single base substitution G C intron_variant OV-AU 3 101378727 101378727 single base substitution C T exon_variant OV-AU 3 101378727 101378727 single base substitution C T missense_variant R649Q 1946G>A OV-AU 3 101388894 101388894 single base substitution A C downstream_gene_variant OV-AU 3 101388894 101388894 single base substitution A C intron_variant OV-AU 3 101394283 101394283 single base substitution A G intron_variant PACA-AU 3 101363622 101363622 single base substitution G A downstream_gene_variant PACA-AU 3 101364068 101364068 single base substitution C A downstream_gene_variant PACA-AU 3 101366691 101366691 single base substitution G A downstream_gene_variant PACA-AU 3 101368310 101368310 single base substitution C A 3_prime_UTR_variant PACA-AU 3 101380933 101380933 deletion of <=200bp G - intron_variant PACA-AU 3 101380933 101380933 deletion of <=200bp G - upstream_gene_variant PACA-AU 3 101381628 101381628 single base substitution C A intron_variant PACA-AU 3 101381628 101381628 single base substitution C A upstream_gene_variant PACA-AU 3 101391906 101391907 deletion of <=200bp AA - intron_variant PACA-AU 3 101392635 101392635 single base substitution G A intron_variant PACA-AU 3 101393281 101393281 single base substitution G A intron_variant PACA-AU 3 101393555 101393555 single base substitution T A intron_variant PACA-AU 3 101393556 101393556 single base substitution A T intron_variant PACA-AU 3 101399313 101399313 single base substitution G C upstream_gene_variant PACA-CA 3 101365400 101365400 single base substitution A C downstream_gene_variant PACA-CA 3 101373440 101373440 single base substitution T A downstream_gene_variant PACA-CA 3 101373440 101373440 single base substitution T A intron_variant PACA-CA 3 101374797 101374797 single base substitution G A exon_variant PACA-CA 3 101374797 101374797 single base substitution G A intron_variant PACA-CA 3 101377603 101377603 deletion of <=200bp G - intron_variant PACA-CA 3 101378442 101378442 deletion of <=200bp T - intron_variant PACA-CA 3 101379830 101379830 insertion of <=200bp - TT intron_variant PACA-CA 3 101379830 101379830 insertion of <=200bp - TT upstream_gene_variant PACA-CA 3 101379983 101379983 single base substitution C T intron_variant PACA-CA 3 101379983 101379983 single base substitution C T upstream_gene_variant PACA-CA 3 101381908 101381908 single base substitution C T intron_variant PACA-CA 3 101381908 101381908 single base substitution C T upstream_gene_variant PACA-CA 3 101389218 101389225 deletion of <=200bp TTCCTAAA - downstream_gene_variant PACA-CA 3 101389218 101389225 deletion of <=200bp TTCCTAAA - intron_variant PACA-CA 3 101391485 101391485 single base substitution C T intron_variant PACA-CA 3 101398939 101398939 single base substitution G C upstream_gene_variant PACA-CA 3 101399998 101399998 single base substitution C T upstream_gene_variant PAEN-AU 3 101363945 101363945 single base substitution G C downstream_gene_variant PAEN-IT 3 101374566 101374566 single base substitution G A downstream_gene_variant PAEN-IT 3 101374566 101374566 single base substitution G A intron_variant PBCA-DE 3 101374697 101374697 insertion of <=200bp - AG exon_variant PBCA-DE 3 101374697 101374697 insertion of <=200bp - AG intron_variant PBCA-DE 3 101375258 101375258 single base substitution A G intron_variant PBCA-DE 3 101393202 101393202 single base substitution C T intron_variant PBCA-DE 3 101396896 101396896 single base substitution C A upstream_gene_variant PBCA-DE 3 101396972 101396972 single base substitution T C upstream_gene_variant PRAD-CA 3 101393559 101393559 single base substitution A T intron_variant PRAD-CA 3 101393560 101393560 single base substitution T A intron_variant PRAD-CA 3 101395668 101395668 single base substitution G A missense_variant R31C 91C>T PRAD-UK 3 101367250 101367250 single base substitution T C downstream_gene_variant PRAD-UK 3 101372540 101372540 single base substitution T C downstream_gene_variant PRAD-UK 3 101372540 101372540 single base substitution T C intron_variant PRAD-UK 3 101375730 101375730 single base substitution C A intron_variant PRAD-UK 3 101383781 101383781 single base substitution C T intron_variant PRAD-UK 3 101396665 101396665 single base substitution G A upstream_gene_variant PRAD-US 3 101383903 101383903 single base substitution G A missense_variant R510C 1528C>T PRAD-US 3 101384241 101384241 single base substitution G C stop_gained S397* 1190C>G READ-US 3 101374969 101374969 single base substitution C A exon_variant READ-US 3 101374969 101374969 single base substitution C A stop_gained E724* 2170G>T READ-US 3 101378679 101378679 single base substitution G T exon_variant READ-US 3 101378679 101378679 single base substitution G T missense_variant S665Y 1994C>A SKCA-BR 3 101363824 101363824 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 3 101364804 101364804 single base substitution G A downstream_gene_variant SKCA-BR 3 101364949 101364949 single base substitution A C downstream_gene_variant SKCA-BR 3 101369305 101369305 single base substitution T A 3_prime_UTR_variant SKCA-BR 3 101369745 101369745 single base substitution C T 3_prime_UTR_variant SKCA-BR 3 101369745 101369745 single base substitution C T downstream_gene_variant SKCA-BR 3 101377990 101377990 single base substitution G A intron_variant SKCA-BR 3 101379765 101379765 single base substitution T C intron_variant SKCA-BR 3 101379765 101379765 single base substitution T C upstream_gene_variant SKCA-BR 3 101379767 101379767 single base substitution G A intron_variant SKCA-BR 3 101379767 101379767 single base substitution G A upstream_gene_variant SKCA-BR 3 101381741 101381741 single base substitution G A intron_variant SKCA-BR 3 101381741 101381741 single base substitution G A upstream_gene_variant SKCA-BR 3 101382442 101382442 single base substitution G A intron_variant SKCA-BR 3 101382442 101382442 single base substitution G A upstream_gene_variant SKCA-BR 3 101392041 101392041 single base substitution C T intron_variant SKCA-BR 3 101392236 101392236 single base substitution G A intron_variant SKCA-BR 3 101392878 101392878 insertion of <=200bp - GTT intron_variant SKCA-BR 3 101393556 101393560 deletion of <=200bp AAAAT - intron_variant SKCA-BR 3 101394743 101394743 single base substitution T C intron_variant SKCM-US 3 101370483 101370483 single base substitution C T downstream_gene_variant SKCM-US 3 101370483 101370483 single base substitution C T missense_variant D897N 2689G>A SKCM-US 3 101378854 101378854 single base substitution G A stop_gained Q607* 1819C>T SKCM-US 3 101378854 101378854 single base substitution G A upstream_gene_variant SKCM-US 3 101383815 101383815 single base substitution A G missense_variant V539A 1616T>C SKCM-US 3 101384215 101384215 single base substitution G A missense_variant H406Y 1216C>T SKCM-US 3 101384430 101384430 single base substitution C T missense_variant R334Q 1001G>A SKCM-US 3 101384585 101384585 single base substitution G T downstream_gene_variant SKCM-US 3 101384585 101384585 single base substitution G T missense_variant F282L 846C>A SKCM-US 3 101390172 101390172 single base substitution G A 3_prime_UTR_variant SKCM-US 3 101390172 101390172 single base substitution G A missense_variant P194S 580C>T SKCM-US 3 101395684 101395684 single base substitution G A synonymous_variant T25T 75C>T SKCM-US 3 101399994 101399994 single base substitution A T upstream_gene_variant STAD-US 3 101370037 101370037 single base substitution C A downstream_gene_variant STAD-US 3 101370037 101370037 single base substitution C A missense_variant E1045D 3135G>T STAD-US 3 101370285 101370285 single base substitution G A downstream_gene_variant STAD-US 3 101370285 101370285 single base substitution G A missense_variant H963Y 2887C>T STAD-US 3 101370325 101370325 insertion of <=200bp - T downstream_gene_variant STAD-US 3 101370325 101370325 insertion of <=200bp - T frameshift_variant K949K? STAD-US 3 101370373 101370373 single base substitution C T downstream_gene_variant STAD-US 3 101370373 101370373 single base substitution C T missense_variant M933I 2799G>A STAD-US 3 101371354 101371354 single base substitution A C downstream_gene_variant STAD-US 3 101371354 101371354 single base substitution A C missense_variant M877R 2630T>G STAD-US 3 101383530 101383530 single base substitution T C missense_variant K551R 1652A>G STAD-US 3 101383530 101383530 single base substitution T C upstream_gene_variant STAD-US 3 101384055 101384055 single base substitution T A missense_variant D459V 1376A>T STAD-US 3 101384247 101384247 single base substitution G A missense_variant A395V 1184C>T STAD-US 3 101389993 101389993 single base substitution C A 3_prime_UTR_variant STAD-US 3 101389993 101389993 single base substitution C A missense_variant E253D 759G>T STAD-US 3 101390079 101390079 single base substitution A G 3_prime_UTR_variant STAD-US 3 101390079 101390079 single base substitution A G missense_variant Y225H 673T>C STAD-US 3 101395663 101395663 single base substitution T G missense_variant K32N 96A>C STAD-US 3 101399981 101399981 single base substitution A G upstream_gene_variant UCEC-US 3 101370125 101370125 single base substitution A C downstream_gene_variant UCEC-US 3 101370125 101370125 single base substitution A C missense_variant I1016S 3047T>G UCEC-US 3 101370427 101370427 single base substitution G T downstream_gene_variant UCEC-US 3 101370427 101370427 single base substitution G T synonymous_variant V915V 2745C>A UCEC-US 3 101373567 101373567 single base substitution G A downstream_gene_variant UCEC-US 3 101373567 101373567 single base substitution G A stop_gained R764* 2290C>T UCEC-US 3 101373629 101373629 single base substitution G T downstream_gene_variant UCEC-US 3 101373629 101373629 single base substitution G T missense_variant S743Y 2228C>A UCEC-US 3 101378635 101378635 single base substitution C T exon_variant UCEC-US 3 101378635 101378635 single base substitution C T missense_variant A680T 2038G>A UCEC-US 3 101378821 101378821 single base substitution G A missense_variant R618C 1852C>T UCEC-US 3 101378821 101378821 single base substitution G A upstream_gene_variant UCEC-US 3 101383509 101383509 single base substitution C A missense_variant R558I 1673G>T UCEC-US 3 101383509 101383509 single base substitution C A upstream_gene_variant UCEC-US 3 101383902 101383902 single base substitution C T missense_variant R510H 1529G>A UCEC-US 3 101384127 101384127 single base substitution G T missense_variant S435Y 1304C>A UCEC-US 3 101390047 101390047 single base substitution A G 3_prime_UTR_variant UCEC-US 3 101390047 101390047 single base substitution A G synonymous_variant N235N 705T>C UCEC-US 3 101390102 101390102 single base substitution G A 3_prime_UTR_variant UCEC-US 3 101390102 101390102 single base substitution G A missense_variant T217I 650C>T UCEC-US 3 101390113 101390113 single base substitution G A 3_prime_UTR_variant UCEC-US 3 101390113 101390113 single base substitution G A synonymous_variant F213F 639C>T UCEC-US 3 101390168 101390168 single base substitution T G 3_prime_UTR_variant UCEC-US 3 101390168 101390168 single base substitution T G missense_variant K195T 584A>C UCEC-US 3 101390177 101390177 single base substitution G T 3_prime_UTR_variant UCEC-US 3 101390177 101390177 single base substitution G T missense_variant S192Y 575C>A UCEC-US 3 101390757 101390757 single base substitution A G intron_variant UCEC-US 3 101390757 101390757 single base substitution A G missense_variant V204A 611T>C UCEC-US 3 101390820 101390820 single base substitution A G missense_variant V183A 548T>C UCEC-US 3 101390820 101390820 single base substitution A G splice_donor_variant UCEC-US 3 101391037 101391037 single base substitution C A missense_variant D111Y 331G>T UCEC-US 3 101395476 101395476 single base substitution A T missense_variant Y95N 283T>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-F5-6814-01 COSM3426837 c.2170G>T p.E724* Substitution - Nonsense 3:101656125-101656125 - 2521249 COSM4136447 c.1946G>A p.R649Q Substitution - Missense 3:101659883-101659883 - BCM265T COSM4949939 c.569A>C p.K190T Substitution - Missense 3:101671339-101671339 - TCGA-BT-A0YX-01 COSM419476 c.639C>T p.F213F Substitution - coding silent 3:101671269-101671269 - TCGA-DZ-6133-01 COSM3992612 c.725T>C p.L242P Substitution - Missense 3:101671183-101671183 - I2L-P10-Tumor-Organoid COSM5355144 c.914A>G p.E305G Substitution - Missense 3:101665673-101665673 - CHC2127T COSM4952804 c.200A>C p.Q67P Substitution - Missense 3:101676715-101676715 - ESCC_25 COSM5626839 c.1642C>G p.Q548E Substitution - Missense 3:101664696-101664696 - J36_T COSM3944608 c.2602A>C p.T868P Substitution - Missense 3:101652538-101652538 - TCGA-BS-A0UV-01 COSM1035813 c.1673G>T p.R558I Substitution - Missense 3:101664665-101664665 - TCGA-EB-A3XC-01 COSM3584662 c.1216C>T p.H406Y Substitution - Missense 3:101665371-101665371 - TCGA-BP-5181-01 COSM1495245 c.1926T>A p.S642S Substitution - coding silent 3:101659903-101659903 - TCGA-A3-3363-01 COSM1495244 c.1801-2A>T p.? Unknown 3:101660030-101660030 - YUKAT COSM5397689 c.2919G>T p.Q973H Substitution - Missense 3:101651409-101651409 - 585223 COSM324354 c.2050T>C p.C684R Substitution - Missense 3:101656245-101656245 - TCGA-DA-A3F8-06 COSM3584664 c.846C>A p.F282L Substitution - Missense 3:101665741-101665741 - LIM1215 COSM4639512 c.2106A>G p.Q702Q Substitution - coding silent 3:101656189-101656189 - SJHGG011_D COSM4969165 c.1166C>T p.S389F Substitution - Missense 3:101665421-101665421 - TCGA-DD-A4NJ-01 COSM4921005 c.1492C>T p.P498S Substitution - Missense 3:101665095-101665095 - TCGA-CM-4743-01 COSM1417465 c.1899G>A p.T633T Substitution - coding silent 3:101659930-101659930 - sysucc-1317T COSM5449765 c.1204A>G p.I402V Substitution - Missense 3:101665383-101665383 - TCGA-G9-6329-01 COSM3673790 c.1190C>G p.S397* Substitution - Nonsense 3:101665397-101665397 - ESO-120 COSM1270689 c.434C>T p.S145F Substitution - Missense 3:101672090-101672090 - T3090 COSM4742067 c.961_963delAAG p.K321delK Deletion - In frame 3:101665624-101665626 - T578 COSM4742066 c.1332G>T p.E444D Substitution - Missense 3:101665255-101665255 - SJHGG011_D COSM4969163 c.880C>T p.H294Y Substitution - Missense 3:101665707-101665707 - LC_S21 COSM1191012 c.3103_3104insT p.A1036fs*8 Insertion - Frameshift 3:101651224-101651225 - Au3 COSM5602622 c.798C>T p.F266F Substitution - coding silent 3:101665789-101665789 - BICR_22 COSM4593371 c.54C>G p.R18R Substitution - coding silent 3:101676861-101676861 - pfg156T COSM4759470 c.646G>A p.V216I Substitution - Missense 3:101671262-101671262 - TCGA-EE-A182-06 COSM3584659 c.2689G>A p.D897N Substitution - Missense 3:101651639-101651639 - I2L-P14b-Tumor-Biopsy COSM5355156 c.2789G>A p.R930H Substitution - Missense 3:101651539-101651539 - TCGA-BS-A0UF-01 COSM1035821 c.584A>C p.K195T Substitution - Missense 3:101671324-101671324 - TCGA-CA-6718-01 COSM1417466 c.1383A>G p.S461S Substitution - coding silent 3:101665204-101665204 - 4132_T COSM3944609 c.1237G>C p.D413H Substitution - Missense 3:101665350-101665350 - 2492721 COSM5723684 c.2694C>T p.A898A Substitution - coding silent 3:101651634-101651634 - TCGA-G7-6797-01 COSM3992610 c.3067G>A p.V1023I Substitution - Missense 3:101651261-101651261 - TCGA-D1-A167-01 COSM1035818 c.705T>C p.N235N Substitution - coding silent 3:101671203-101671203 - OSCC-GB_01160111 COSM5956056 c.271C>G p.Q91E Substitution - Missense 3:101676644-101676644 - TCGA-CD-5801-01 COSM4111900 c.2630T>G p.M877R Substitution - Missense 3:101652510-101652510 - TCGA-BS-A0UV-01 COSM1035807 c.2228C>A p.S743Y Substitution - Missense 3:101654785-101654785 - S02350 COSM5694792 c.1220C>T p.P407L Substitution - Missense 3:101665367-101665367 - PT26 COSM5943640 c.2645-3delT p.? Unknown 3:101651686-101651686 - TCGA-GF-A6C9-06 COSM4902816 c.75C>T p.T25T Substitution - coding silent 3:101676840-101676840 - P146 COSM1735797 c.2645-3_2645-2insT p.? Unknown 3:101651685-101651686 - MO_1094 COSM5574046 c.1746_1747insA p.A583fs*10 Insertion - Frameshift 3:101664591-101664592 - TCGA-AP-A059-01 COSM1035808 c.2038G>A p.A680T Substitution - Missense 3:101659791-101659791 - TCGA-AN-A046-01 COSM2915683 c.2780G>A p.R927Q Substitution - Missense 3:101651548-101651548 - TCGA-CK-5913-01 COSM5829558 c.2645-6_2645-3delTTTT p.? Unknown 3:101651686-101651689 - TCGA-66-2767-01 COSM727535 c.832C>T p.L278L Substitution - coding silent 3:101665755-101665755 - 2492722 COSM5723684 c.2694C>T p.A898A Substitution - coding silent 3:101651634-101651634 - TCGA-C5-A1BQ-01 COSM4842385 c.1286G>C p.R429T Substitution - Missense 3:101665301-101665301 - ZZUFHECRKL-G039T COSM5437769 c.2645-2A>T p.? Unknown 3:101651685-101651685 - TCGA-GD-A2C5-01 COSM1308329 c.1958G>A p.C653Y Substitution - Missense 3:101659871-101659871 - TCGA-B6-A1KN-01 COSM1484380 c.2067C>G p.I689M Substitution - Missense 3:101656228-101656228 - 43 COSM5734001 c.986C>G p.S329C Substitution - Missense 3:101665601-101665601 - TCGA-BS-A0UV-01 COSM419476 c.639C>T p.F213F Substitution - coding silent 3:101671269-101671269 - 6_tFL COSM4171190 c.2685G>A p.W895* Substitution - Nonsense 3:101651643-101651643 - TCGA-CA-6717-01 COSM1417467 c.1079A>G p.D360G Substitution - Missense 3:101665508-101665508 - TCGA-AS-3777-01 COSM1495244 c.1801-2A>T p.? Unknown 3:101660030-101660030 - TCGA-BQ-5875-01 COSM3992611 c.2021C>G p.T674R Substitution - Missense 3:101659808-101659808 - TCGA-66-2765-01 COSM727536 c.1555C>T p.R519* Substitution - Nonsense 3:101665032-101665032 - pfg043T COSM4759469 c.1179A>C p.E393D Substitution - Missense 3:101665408-101665408 - LP6005690-DNA_C02 COSM4411799 c.2628C>T p.H876H Substitution - coding silent 3:101652512-101652512 - 2492723 COSM5723684 c.2694C>T p.A898A Substitution - coding silent 3:101651634-101651634 - ESO-251 COSM1270688 c.717delT p.R240fs*39 Deletion - Frameshift 3:101671191-101671191 - BCM265T COSM4949939 c.569A>C p.K190T Substitution - Missense 3:101671339-101671339 - SNUH_G26_S1 COSM4002354 c.1624-4C>T p.? Unknown 3:101664718-101664718 - TCGA-F5-6814-01 COSM3426838 c.1994C>A p.S665Y Substitution - Missense 3:101659835-101659835 - LOVO COSM2915731 c.427C>A p.L143I Substitution - Missense 3:101672097-101672097 - TCGA-CG-4455-01 COSM4111904 c.1376A>T p.D459V Substitution - Missense 3:101665211-101665211 - pfg068T COSM4759468 c.1439C>A p.P480H Substitution - Missense 3:101665148-101665148 - TCGA-B7-5816-01 COSM4111907 c.673T>C p.Y225H Substitution - Missense 3:101671235-101671235 - SJHGG011_D COSM4969166 c.883C>T p.L295F Substitution - Missense 3:101665704-101665704 - S00539 COSM316637 c.384A>T p.P128P Substitution - coding silent 3:101672140-101672140 - TCGA-DB-A64W-01 COSM1035806 c.2290C>T p.R764* Substitution - Nonsense 3:101654723-101654723 - S00944 COSM5664184 c.214C>T p.R72W Substitution - Missense 3:101676701-101676701 - TCGA-D1-A17T-01 COSM1035817 c.1055C>A p.T352K Substitution - Missense 3:101665532-101665532 - CSCC-31-T COSM4540950 c.2919G>A p.Q973Q Substitution - coding silent 3:101651409-101651409 - TCGA-AA-3966-01 COSM273480 c.1747G>A p.A583T Substitution - Missense 3:101664591-101664591 - B74-Tumor COSM1752756 c.430G>A p.E144K Substitution - Missense 3:101672094-101672094 - S02279 COSM5683742 c.2078G>T p.G693V Substitution - Missense 3:101656217-101656217 - TCGA-85-6175-01 COSM727533 c.661G>A p.E221K Substitution - Missense 3:101671247-101671247 - T10 COSM5344287 c.235C>T p.H79Y Substitution - Missense 3:101676680-101676680 - 1N55-VS-1T55 COSM4977102 c.487C>A p.P163T Substitution - Missense 3:101672037-101672037 - TCGA-22-4604-01 COSM727534 c.751A>T p.S251C Substitution - Missense 3:101671157-101671157 - TCGA-AX-A0J1-01 COSM1035815 c.1529G>A p.R510H Substitution - Missense 3:101665058-101665058 - TCGA-63-5128-01 COSM727538 c.3143A>G p.H1048R Substitution - Missense 3:101651185-101651185 - S00539 COSM316637 c.384A>T p.P128P Substitution - coding silent 3:101672140-101672140 - RK154_C01 COSM3766823 c.3041A>G p.Q1014R Substitution - Missense 3:101651287-101651287 - C086 COSM5541912 c.1214C>T p.S405F Substitution - Missense 3:101665373-101665373 - TCGA-AX-A0J0-01 COSM1035816 c.1304C>A p.S435Y Substitution - Missense 3:101665283-101665283 - ESCC-180T COSM3940179 c.662A>T p.E221V Substitution - Missense 3:101671246-101671246 - SNU-175 COSM2915679 c.3090G>A p.Q1030Q Substitution - coding silent 3:101651238-101651238 - TCGA-BS-A0TJ-01 COSM1035819 c.699A>G p.S233S Substitution - coding silent 3:101671209-101671209 - CPCG0191-F1 COSM4880938 c.91C>T p.R31C Substitution - Missense 3:101676824-101676824 - TCGA-FU-A3YQ-01 COSM727536 c.1555C>T p.R519* Substitution - Nonsense 3:101665032-101665032 - TCGA-HC-7749-01 COSM3673789 c.2000G>T p.R667L Substitution - Missense 3:101659829-101659829 - HCC2998 COSM1670388 c.2488G>T p.E830* Substitution - Nonsense 3:101652652-101652652 - CSCC-35-T COSM4565868 c.2637_2638CC>TT p.H880Y Substitution - Missense 3:101652502-101652503 - TCGA-A5-A0R7-01 COSM1035810 c.1838G>C p.R613P Substitution - Missense 3:101659991-101659991 - J38_T COSM3944610 c.873A>C p.L291F Substitution - Missense 3:101665714-101665714 - TCGA-CG-5721-01 COSM4111905 c.1184C>T p.A395V Substitution - Missense 3:101665403-101665403 - TCGA-DM-A1D0-01 COSM1417463 c.3092A>C p.K1031T Substitution - Missense 3:101651236-101651236 - TCGA-B0-5697-01 COSM479162 c.446G>A p.S149N Substitution - Missense 3:101672078-101672078 - 5853_PT COSM5756133 c.1649G>A p.G550E Substitution - Missense 3:101664689-101664689 - HCC074T COSM5810205 c.2054G>A p.G685E Substitution - Missense 3:101656241-101656241 - TCGA-FW-A3R5-06 COSM3914409 c.580C>T p.P194S Substitution - Missense 3:101671328-101671328 - TCGA-BS-A0UF-01 COSM1035824 c.331G>T p.D111Y Substitution - Missense 3:101672193-101672193 - cSCCP8 COSM140456 c.3133G>A p.E1045K Substitution - Missense 3:101651195-101651195 - TCGA-BR-6452-01 COSM4111897 c.3135G>T p.E1045D Substitution - Missense 3:101651193-101651193 - TCGA-B5-A11E-01 COSM1035820 c.650C>T p.T217I Substitution - Missense 3:101671258-101671258 - TCGA-IR-A3LK-01 COSM4817796 c.2178G>C p.M726I Substitution - Missense 3:101656117-101656117 - WSU-HN8 COSM4593371 c.54C>G p.R18R Substitution - coding silent 3:101676861-101676861 - 20T COSM3714331 c.729T>C p.F243F Substitution - coding silent 3:101671179-101671179 - T3064 COSM4742068 c.374G>A p.R125Q Substitution - Missense 3:101672150-101672150 - TCGA-25-1635-01 COSM117983 c.2779C>T p.R927* Substitution - Nonsense 3:101651549-101651549 - CHC2127T COSM4952804 c.200A>C p.Q67P Substitution - Missense 3:101676715-101676715 - TCGA-AA-3976-01 COSM297540 c.900C>A p.V300V Substitution - coding silent 3:101665687-101665687 - SWE-2A COSM1178189 c.1158C>A p.P386P Substitution - coding silent 3:101665429-101665429 - B74 COSM1752756 c.430G>A p.E144K Substitution - Missense 3:101672094-101672094 - sysucc-1317T COSM5449766 c.719G>A p.R240Q Substitution - Missense 3:101671189-101671189 - pfg017T COSM1642035 c.1274C>T p.T425I Substitution - Missense 3:101665313-101665313 - 12T COSM107509 c.382C>T p.P128S Substitution - Missense 3:101672142-101672142 - TCGA-A5-A0G9-01 COSM1035805 c.2708G>A p.R903H Substitution - Missense 3:101651620-101651620 - OSCC-GB_00200111 COSM3714331 c.729T>C p.F243F Substitution - coding silent 3:101671179-101671179 - TCGA-AA-3715-01 COSM270573 c.2854C>A p.L952I Substitution - Missense 3:101651474-101651474 - TCGA-BR-7707-01 COSM4111898 c.2887C>T p.H963Y Substitution - Missense 3:101651441-101651441 - TCGA-HU-A4GX-01 COSM4111906 c.759G>T p.E253D Substitution - Missense 3:101671149-101671149 - TCGA-EE-A2GS-06 COSM3584661 c.1616T>C p.V539A Substitution - Missense 3:101664971-101664971 - LS411 COSM2915708 c.1584G>A p.L528L Substitution - coding silent 3:101665003-101665003 - TCGA-CM-4748-01 COSM3695733 c.966C>T p.G322G Substitution - coding silent 3:101665621-101665621 - TCGA-BS-A0UL-01 COSM1035825 c.283T>A p.Y95N Substitution - Missense 3:101676632-101676632 - TCGA-AP-A051-01 COSM1035823 c.546+2T>C p.? Unknown 3:101671976-101671976 - PA285 COSM1163317 c.3058G>A p.V1020I Substitution - Missense 3:101651270-101651270 - TCGA-HC-7231-01 COSM1471480 c.1528C>T p.R510C Substitution - Missense 3:101665059-101665059 - SJHGG011_D COSM4969164 c.779-7C>G p.? Unknown 3:101665815-101665815 - OV207 COSM253123 c.2645-5_2645-3delTTT p.? Unknown 3:101651686-101651688 - UM-SCC-4 COSM4593371 c.54C>G p.R18R Substitution - coding silent 3:101676861-101676861 - TCGA-B5-A0JY-01 COSM1035806 c.2290C>T p.R764* Substitution - Nonsense 3:101654723-101654723 - 5202_PT COSM5756133 c.1649G>A p.G550E Substitution - Missense 3:101664689-101664689 - TCGA-D8-A1JK-01 COSM1484378 c.2868C>T p.N956N Substitution - coding silent 3:101651460-101651460 - ESCC_65 COSM4593371 c.54C>G p.R18R Substitution - coding silent 3:101676861-101676861 - HCC56 COSM1616667 c.939G>C p.E313D Substitution - Missense 3:101665648-101665648 - HCC2998 COSM1670388 c.2488G>T p.E830* Substitution - Nonsense 3:101652652-101652652 - LIM1899 COSM4640471 c.1945C>T p.R649W Substitution - Missense 3:101659884-101659884 - HN_62686 COSM130273 c.2590G>A p.G864R Substitution - Missense 3:101652550-101652550 - TCGA-A1-A0SJ-01 COSM445219 c.1818T>G p.F606L Substitution - Missense 3:101660011-101660011 - UM-SCC-47 COSM4593371 c.54C>G p.R18R Substitution - coding silent 3:101676861-101676861 - TCGA-BR-6452-01 COSM4111899 c.2799G>A p.M933I Substitution - Missense 3:101651529-101651529 - LUAD-S01315 COSM345377 c.2250C>T p.L750L Substitution - coding silent 3:101654763-101654763 - HCC56T COSM1616667 c.939G>C p.E313D Substitution - Missense 3:101665648-101665648 - LUAD-YINHD COSM350688 c.2349G>A p.Q783Q Substitution - coding silent 3:101652899-101652899 - 9642_PT COSM5756133 c.1649G>A p.G550E Substitution - Missense 3:101664689-101664689 - TCGA-29-1763-01 COSM1327144 c.3124G>C p.V1042L Substitution - Missense 3:101651204-101651204 - TCGA-D8-A1XW-01 COSM1484379 c.2823G>A p.V941V Substitution - coding silent 3:101651505-101651505 - NYU1363 COSM4770951 c.1689C>T p.N563N Substitution - coding silent 3:101664649-101664649 - 526LT COSM4382960 c.2808C>A p.F936L Substitution - Missense 3:101651520-101651520 - TCGA-B5-A11E-01 COSM1035804 c.2745C>A p.V915V Substitution - coding silent 3:101651583-101651583 - CSCC-55-T COSM4533368 c.1973G>A p.R658K Substitution - Missense 3:101659856-101659856 - LUAD-B01970 COSM356143 c.2688T>C p.A896A Substitution - coding silent 3:101651640-101651640 - SJOS005_D COSM5024326 c.2228C>T p.S743F Substitution - Missense 3:101654785-101654785 - TCGA-D1-A17Q-01 COSM1035822 c.575C>A p.S192Y Substitution - Missense 3:101671333-101671333 - P129 COSM253123 c.2645-5_2645-3delTTT p.? Unknown 3:101651686-101651688 - TCGA-BS-A0UV-01 COSM1035809 c.1852C>T p.R618C Substitution - Missense 3:101659977-101659977 - TCGA-AX-A05Z-01 COSM1035803 c.3047T>G p.I1016S Substitution - Missense 3:101651281-101651281 - TCGA-AG-A002-01 COSM264761 c.2164C>A p.L722I Substitution - Missense 3:101656131-101656131 - TCGA-FS-A1ZP-06 COSM3584660 c.1819C>T p.Q607* Substitution - Nonsense 3:101660010-101660010 - 1N64-VS-1T64 COSM1417465 c.1899G>A p.T633T Substitution - coding silent 3:101659930-101659930 - TCGA-BR-8680-01 COSM4111908 c.96A>C p.K32N Substitution - Missense 3:101676819-101676819 - TCGA-21-5782-01 COSM727537 c.2101C>T p.H701Y Substitution - Missense 3:101656194-101656194 - TCGA-FP-8211-01 COSM4111903 c.1652A>G p.K551R Substitution - Missense 3:101664686-101664686 - D12 COSM5006828 c.2042G>A p.C681Y Substitution - Missense 3:101659787-101659787 - TCGA-FS-A1ZZ-06 COSM3584663 c.1001G>A p.R334Q Substitution - Missense 3:101665586-101665586 - UM-SCC-11B COSM4593371 c.54C>G p.R18R Substitution - coding silent 3:101676861-101676861 - TCGA-D1-A17M-01 COSM1035814 c.1544G>T p.G515V Substitution - Missense 3:101665043-101665043 - 587332 COSM1233123 c.2174A>G p.H725R Substitution - Missense 3:101656121-101656121 - TCGA-BT-A20P-01 COSM419477 c.2686G>A p.A896T Substitution - Missense 3:101651642-101651642 - T3091 COSM4742065 c.1746C>T p.Y582Y Substitution - coding silent 3:101664592-101664592 - AOCS-134-3-9 COSM4136447 c.1946G>A p.R649Q Substitution - Missense 3:101659883-101659883 - 2492720 COSM5723684 c.2694C>T p.A898A Substitution - coding silent 3:101651634-101651634 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.655286 3q12.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F606L c.1818T>G 3 101378855 BRCA A C Missense p.M877R c.2630T>G 3 101371354 STAD A C Synonymous p.A835A c.2505T>G 3 101371479 CM A - Frameshift p.R240Efs*39 c.717delT 3 101390035 ESCA A G Missense p.C684R c.2050T>C 3 101375089 SCLC A G Missense p.V539A c.1616T>C 3 101383815 CM A G Missense p.Y225H c.673T>C 3 101390079 STAD A T Missense p.Y95N c.283T>A 3 101395476 UCEC C A Missense p.A1036S c.3106G>T 3 101370066 LUAD C A Missense p.R649L c.1946G>T 3 101378727 LUAD C A Missense p.R667L c.2000G>T 3 101378673 PRAD C A Missense p.R927L c.2780G>T 3 101370392 HNSC C A Nonsense p.E732* c.2194G>T 3 101373663 HNSC C G Missense p.K686N c.2058G>C 3 101375081 HNSC C T IntronicSNV . c.778+139G>A 3 101389835 HC C T Missense p.A896T c.2686G>A 3 101370486 BLCA C T Missense p.C653Y c.1958G>A 3 101378715 BLCA C T Missense p.D897N c.2689G>A 3 101370483 CM C T Missense p.E221K c.661G>A 3 101390091 LUSC C T Missense p.E444K c.1330G>A 3 101384101 HNSC C T Missense p.G864R c.2590G>A 3 101371394 HNSC C T Missense p.R334Q c.1001G>A 3 101384430 CM C T Missense p.R429K c.1286G>A 3 101384145 CM C T Missense p.R549K c.1646G>A 3 101383536 CM C T Synonymous p.V941V c.2823G>A 3 101370349 BRCA G A Missense p.H701Y c.2101C>T 3 101375038 LUSC G A Missense p.P82L c.245C>T 3 101395514 BRCA G A Missense p.R510C c.1528C>T 3 101383903 PRAD G A Missense p.S145F c.434C>T 3 101390934 ESCA G A Missense p.S642F c.1925C>T 3 101378748 CM G A Missense p.T425I c.1274C>T 3 101384157 STAD G A Nonsense p.Q607* c.1819C>T 3 101378854 CM G A Nonsense p.R519* c.1555C>T 3 101383876 LUSC G A Nonsense p.R927* c.2779C>T 3 101370393 OV G A Synonymous p.F213F c.639C>T 3 101390113 BLCA G A Synonymous p.L278L c.832C>T 3 101384599 LUSC G A Synonymous p.N956N c.2868C>T 3 101370304 BRCA G A Synonymous p.V683V c.2049C>T 3 101375090 CM G C Missense p.I689M c.2067C>G 3 101375072 BRCA G C Nonsense p.S397* c.1190C>G 3 101384241 PRAD G T Missense p.F282L c.846C>A 3 101384585 CM G T Synonymous p.V300V c.900C>A 3 101384531 COREAD T A Missense p.D459V c.1376A>T 3 101384055 STAD T A Missense p.L1024F c.3072A>T 3 101370100 LUAD T A Missense p.S251C c.751A>T 3 101390001 LUSC T A Nonsense p.K177* c.529A>T 3 101390839 HNSC T A Synonymous p.P128P c.384A>T 3 101390984 SCLC T C Missense p.H1048R c.3143A>G 3 101370029 LUSC