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 69074854 69074854 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr3:69074854G>A c.2869C>T c.(2869-2871)Cat>Tat p.H957Y BLCA 3 69082820 69082820 + Silent SNP C C T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr3:69082820C>T c.2280G>A c.(2278-2280)ctG>ctA p.L760L BLCA 3 69082857 69082860 + Splice_Site DEL TGAA TGAA - TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr3:69082857_69082860delTGAA c.e10-2 BLCA 3 69087847 69087847 + Silent SNP G G A TCGA-E7-A97P-01A-11D-A38G-08 TCGA-E7-A97P-10A-01D-A38J-08 g.chr3:69087847G>A c.2019C>T c.(2017-2019)gcC>gcT p.A673A BLCA 3 69088046 69088046 + Missense_Mutation SNP C C T TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr3:69088046C>T c.1942G>A c.(1942-1944)Gaa>Aaa p.E648K BLCA 3 69088121 69088121 + Nonsense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr3:69088121C>A c.1867G>T c.(1867-1869)Gaa>Taa p.E623* BLCA 3 69088776 69088776 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr3:69088776C>G c.1753G>C c.(1753-1755)Gag>Cag p.E585Q BLCA 3 69093692 69093692 + Missense_Mutation SNP G G C TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr3:69093692G>C c.1402C>G c.(1402-1404)Ctt>Gtt p.L468V BLCA 3 69097054 69097054 + Missense_Mutation SNP T T C TCGA-ZF-AA52-01A-12D-A391-08 TCGA-ZF-AA52-10A-01D-A394-08 g.chr3:69097054T>C c.802A>G c.(802-804)Ata>Gta p.I268V BLCA 3 69097297 69097297 + Missense_Mutation SNP T T C TCGA-GV-A3QH-01A-11D-A21Z-08 TCGA-GV-A3QH-10A-01D-A21Z-08 g.chr3:69097297T>C c.559A>G c.(559-561)Atg>Gtg p.M187V BLCA 3 69097557 69097557 + Missense_Mutation SNP A A T TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr3:69097557A>T c.299T>A c.(298-300)tTt>tAt p.F100Y BRCA 3 69072340 69072340 + Silent SNP T T C TCGA-AR-A252-01A-11D-A167-09 TCGA-AR-A252-10A-01D-A167-09 g.chr3:69072340T>C c.3270A>G c.(3268-3270)caA>caG p.Q1090Q BRCA 3 69084265 69084265 + Splice_Site SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr3:69084265A>C c.2153T>G c.(2152-2154)gTg>gGg p.V718G BRCA 3 69088027 69088027 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr3:69088027C>T c.1961G>A c.(1960-1962)cGa>cAa p.R654Q BRCA 3 69096739 69096739 + Missense_Mutation SNP C C T TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr3:69096739C>T c.1117G>A c.(1117-1119)Gct>Act p.A373T BRCA 3 69097500 69097500 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr3:69097500G>A c.356C>T c.(355-357)cCa>cTa p.P119L CESC 3 69073265 69073265 + Missense_Mutation SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr3:69073265G>C c.3079C>G c.(3079-3081)Caa>Gaa p.Q1027E CESC 3 69075149 69075149 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr3:69075149G>C c.2857C>G c.(2857-2859)Cag>Gag p.Q953E CESC 3 69093647 69093647 + Missense_Mutation SNP T T G TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr3:69093647T>G c.1447A>C c.(1447-1449)Aaa>Caa p.K483Q CESC 3 69101209 69101209 + Missense_Mutation SNP G G C TCGA-Q1-A6DW-01A-11D-A32I-09 TCGA-Q1-A6DW-10B-01D-A32I-09 g.chr3:69101209G>C c.29C>G c.(28-30)tCc>tGc p.S10C COAD 3 69072455 69072455 + Missense_Mutation SNP T T C TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr3:69072455T>C c.3155A>G c.(3154-3156)tAc>tGc p.Y1052C COAD 3 69073286 69073286 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:69073286C>T c.3058G>A c.(3058-3060)Gaa>Aaa p.E1020K COAD 3 69074743 69074743 + Nonsense_Mutation SNP T T A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr3:69074743T>A c.2980A>T c.(2980-2982)Aag>Tag p.K994* COAD 3 69074854 69074854 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr3:69074854G>A c.2869C>T c.(2869-2871)Cat>Tat p.H957Y COAD 3 69077112 69077112 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr3:69077112C>A c.2696G>T c.(2695-2697)aGa>aTa p.R899I COAD 3 69084177 69084177 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr3:69084177C>T c.2241G>A c.(2239-2241)caG>caA p.Q747Q COAD 3 69087843 69087843 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:69087843C>T c.2023G>A c.(2023-2025)Gct>Act p.A675T COAD 3 69088067 69088067 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr3:69088067G>A c.1921C>T c.(1921-1923)Cgt>Tgt p.R641C COAD 3 69088121 69088121 + Nonsense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:69088121C>A c.1867G>T c.(1867-1869)Gaa>Taa p.E623* COAD 3 69088715 69088715 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:69088715T>C c.1814A>G c.(1813-1815)cAg>cGg p.Q605R COAD 3 69088798 69088798 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:69088798C>A c.1731G>T c.(1729-1731)aaG>aaT p.K577N COAD 3 69092915 69092915 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr3:69092915C>T c.1564G>A c.(1564-1566)Gat>Aat p.D522N COAD 3 69092962 69092962 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:69092962C>A c.1517G>T c.(1516-1518)aGa>aTa p.R506I COAD 3 69096775 69096775 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:69096775T>G c.1081A>C c.(1081-1083)Aat>Cat p.N361H COAD 3 69097150 69097150 + Missense_Mutation SNP C C A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:69097150C>A c.706G>T c.(706-708)Gac>Tac p.D236Y COAD 3 69097670 69097670 + Nonsense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr3:69097670C>T c.186G>A c.(184-186)tgG>tgA p.W62* COADREAD 3 69072455 69072455 + Missense_Mutation SNP T T C TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr3:69072455T>C c.3155A>G c.(3154-3156)tAc>tGc p.Y1052C COADREAD 3 69073286 69073286 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:69073286C>T c.3058G>A c.(3058-3060)Gaa>Aaa p.E1020K COADREAD 3 69074743 69074743 + Nonsense_Mutation SNP T T A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr3:69074743T>A c.2980A>T c.(2980-2982)Aag>Tag p.K994* COADREAD 3 69074854 69074854 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr3:69074854G>A c.2869C>T c.(2869-2871)Cat>Tat p.H957Y COADREAD 3 69077112 69077112 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr3:69077112C>A c.2696G>T c.(2695-2697)aGa>aTa p.R899I COADREAD 3 69084177 69084177 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr3:69084177C>T c.2241G>A c.(2239-2241)caG>caA p.Q747Q COADREAD 3 69087843 69087843 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:69087843C>T c.2023G>A c.(2023-2025)Gct>Act p.A675T COADREAD 3 69088067 69088067 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr3:69088067G>A c.1921C>T c.(1921-1923)Cgt>Tgt p.R641C COADREAD 3 69088121 69088121 + Nonsense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:69088121C>A c.1867G>T c.(1867-1869)Gaa>Taa p.E623* COADREAD 3 69088715 69088715 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:69088715T>C c.1814A>G c.(1813-1815)cAg>cGg p.Q605R COADREAD 3 69088798 69088798 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:69088798C>A c.1731G>T c.(1729-1731)aaG>aaT p.K577N COADREAD 3 69092915 69092915 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr3:69092915C>T c.1564G>A c.(1564-1566)Gat>Aat p.D522N COADREAD 3 69092962 69092962 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:69092962C>A c.1517G>T c.(1516-1518)aGa>aTa p.R506I COADREAD 3 69096730 69096730 + Missense_Mutation SNP T T C TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr3:69096730T>C c.1126A>G c.(1126-1128)Aaa>Gaa p.K376E COADREAD 3 69096775 69096775 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:69096775T>G c.1081A>C c.(1081-1083)Aat>Cat p.N361H COADREAD 3 69097150 69097150 + Missense_Mutation SNP C C A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:69097150C>A c.706G>T c.(706-708)Gac>Tac p.D236Y COADREAD 3 69097670 69097670 + Nonsense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr3:69097670C>T c.186G>A c.(184-186)tgG>tgA p.W62* DLBC 3 69073223 69073223 + Missense_Mutation SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr3:69073223G>A c.3121C>T c.(3121-3123)Ctt>Ttt p.L1041F ESCA 3 69072373 69072373 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr3:69072373C>T c.3237G>A c.(3235-3237)atG>atA p.M1079I ESCA 3 69079117 69079117 + Missense_Mutation SNP G G A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr3:69079117G>A c.2443C>T c.(2443-2445)Cgt>Tgt p.R815C ESCA 3 69088134 69088134 + Silent SNP C C T TCGA-LN-A4A3-01A-11D-A27G-09 TCGA-LN-A4A3-10A-01D-A27G-09 g.chr3:69088134C>T c.1854G>A c.(1852-1854)gaG>gaA p.E618E ESCA 3 69088142 69088142 + Nonsense_Mutation SNP C C A TCGA-Z6-A8JD-01A-11D-A36J-09 TCGA-Z6-A8JD-10A-01D-A36M-09 g.chr3:69088142C>A c.1846G>T c.(1846-1848)Gag>Tag p.E616* ESCA 3 69097567 69097567 + Missense_Mutation SNP A A C TCGA-L5-A4OG-01A-11D-A27G-09 TCGA-L5-A4OG-11A-12D-A27G-09 g.chr3:69097567A>C c.289T>G c.(289-291)Ttc>Gtc p.F97V GBM 3 69075241 69075241 + Missense_Mutation SNP T T C TCGA-06-2559-01A-01D-1494-08 TCGA-06-2559-10A-01D-1494-08 g.chr3:69075241T>C c.2765A>G c.(2764-2766)aAg>aGg p.K922R GBM 3 69097037 69097037 + Silent SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr3:69097037C>T c.819G>A c.(817-819)gcG>gcA p.A273A GBM 3 69097485 69097485 + Missense_Mutation SNP C C T TCGA-76-6664-01A-11D-1845-08 TCGA-76-6664-10A-01D-1845-08 g.chr3:69097485C>T c.371G>A c.(370-372)cGa>cAa p.R124Q GBMLGG 3 69075205 69075205 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:69075205C>T c.2801G>A c.(2800-2802)cGc>cAc p.R934H GBMLGG 3 69075241 69075241 + Missense_Mutation SNP T T C TCGA-06-2559-01A-01D-1494-08 TCGA-06-2559-10A-01D-1494-08 g.chr3:69075241T>C c.2765A>G c.(2764-2766)aAg>aGg p.K922R GBMLGG 3 69079032 69079032 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:69079032C>T c.2528G>A c.(2527-2529)aGt>aAt p.S843N GBMLGG 3 69088055 69088055 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:69088055C>A c.1933G>T c.(1933-1935)Gac>Tac p.D645Y GBMLGG 3 69097037 69097037 + Silent SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr3:69097037C>T c.819G>A c.(817-819)gcG>gcA p.A273A GBMLGG 3 69097485 69097485 + Missense_Mutation SNP C C T TCGA-76-6664-01A-11D-1845-08 TCGA-76-6664-10A-01D-1845-08 g.chr3:69097485C>T c.371G>A c.(370-372)cGa>cAa p.R124Q HNSC 3 69084235 69084235 + Missense_Mutation SNP G G C TCGA-MZ-A7D7-01A-21D-A34J-08 TCGA-MZ-A7D7-10A-01D-A34M-08 g.chr3:69084235G>C c.2183C>G c.(2182-2184)aCa>aGa p.T728R HNSC 3 69088019 69088019 + Nonsense_Mutation SNP G G A TCGA-CV-5442-01A-01D-1512-08 TCGA-CV-5442-11A-01D-1512-08 g.chr3:69088019G>A c.1969C>T c.(1969-1971)Cag>Tag p.Q657* HNSC 3 69088066 69088066 + Missense_Mutation SNP C C T TCGA-D6-A74Q-01A-11D-A34J-08 TCGA-D6-A74Q-10A-02D-A34M-08 g.chr3:69088066C>T c.1922G>A c.(1921-1923)cGt>cAt p.R641H HNSC 3 69097184 69097184 + Silent SNP G G A TCGA-F7-A623-01A-11D-A28R-08 TCGA-F7-A623-10A-01D-A28U-08 g.chr3:69097184G>A c.672C>T c.(670-672)gaC>gaT p.D224D HNSC 3 69097622 69097622 + Silent SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr3:69097622A>G c.234T>C c.(232-234)ccT>ccC p.P78P HNSC 3 69101126 69101126 + Missense_Mutation SNP A A T TCGA-HD-A633-01A-11D-A28R-08 TCGA-HD-A633-10A-01D-A28U-08 g.chr3:69101126A>T c.112T>A c.(112-114)Tgg>Agg p.W38R KIPAN 3 69072460 69072460 + Silent SNP T T C TCGA-A4-A6HP-01A-11D-A31X-10 TCGA-A4-A6HP-10A-01D-A31X-10 g.chr3:69072460T>C c.3150A>G c.(3148-3150)caA>caG p.Q1050Q KIPAN 3 69073260 69073260 + Missense_Mutation SNP A A C TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chr3:69073260A>C c.3084T>G c.(3082-3084)aaT>aaG p.N1028K KIPAN 3 69088741 69088741 + Frame_Shift_Del DEL T T - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr3:69088741delT c.1788delA c.(1786-1788)aaafs p.K596fs KIPAN 3 69092928 69092928 + Silent SNP G G A TCGA-SX-A7SP-01A-11D-A34Z-10 TCGA-SX-A7SP-10A-01D-A34Z-10 g.chr3:69092928G>A c.1551C>T c.(1549-1551)gcC>gcT p.A517A KIPAN 3 69096518 69096518 + Missense_Mutation SNP A A C TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr3:69096518A>C c.1338T>G c.(1336-1338)gaT>gaG p.D446E KIPAN 3 69096707 69096707 + Silent SNP T T C TCGA-B9-4116-01A-01D-1252-08 TCGA-B9-4116-10A-01D-1252-08 g.chr3:69096707T>C c.1149A>G c.(1147-1149)acA>acG p.T383T KIPAN 3 69096768 69096770 + In_Frame_Del DEL GAA GAA - TCGA-A4-7997-01A-11D-2201-08 TCGA-A4-7997-10A-01D-2201-08 g.chr3:69096768_69096770delGAA c.1086_1088delTTC c.(1084-1089)tcttca>tca p.362_363SS>S KIPAN 3 69097304 69097307 + Frame_Shift_Del DEL TTCT TTCT - TCGA-Y8-A8S1-01A-11D-A36X-10 TCGA-Y8-A8S1-10A-01D-A370-10 g.chr3:69097304_69097307delTTCT c.549_552delAGAA c.(547-552)aaagaafs p.KE183fs KIPAN 3 69101211 69101211 + Silent SNP G G A TCGA-BQ-5878-01A-11D-1589-08 TCGA-BQ-5878-11A-01D-1589-08 g.chr3:69101211G>A c.27C>T c.(25-27)ctC>ctT p.L9L KIRC 3 69073260 69073260 + Missense_Mutation SNP A A C TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chr3:69073260A>C c.3084T>G c.(3082-3084)aaT>aaG p.N1028K KIRC 3 69088741 69088741 + Frame_Shift_Del DEL T T - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr3:69088741delT c.1788delA c.(1786-1788)aaafs p.K596fs KIRP 3 69072460 69072460 + Silent SNP T T C TCGA-A4-A6HP-01A-11D-A31X-10 TCGA-A4-A6HP-10A-01D-A31X-10 g.chr3:69072460T>C c.3150A>G c.(3148-3150)caA>caG p.Q1050Q KIRP 3 69092928 69092928 + Silent SNP G G A TCGA-SX-A7SP-01A-11D-A34Z-10 TCGA-SX-A7SP-10A-01D-A34Z-10 g.chr3:69092928G>A c.1551C>T c.(1549-1551)gcC>gcT p.A517A KIRP 3 69096518 69096518 + Missense_Mutation SNP A A C TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr3:69096518A>C c.1338T>G c.(1336-1338)gaT>gaG p.D446E KIRP 3 69096707 69096707 + Silent SNP T T C TCGA-B9-4116-01A-01D-1252-08 TCGA-B9-4116-10A-01D-1252-08 g.chr3:69096707T>C c.1149A>G c.(1147-1149)acA>acG p.T383T KIRP 3 69096768 69096770 + In_Frame_Del DEL GAA GAA - TCGA-A4-7997-01A-11D-2201-08 TCGA-A4-7997-10A-01D-2201-08 g.chr3:69096768_69096770delGAA c.1086_1088delTTC c.(1084-1089)tcttca>tca p.362_363SS>S KIRP 3 69097304 69097307 + Frame_Shift_Del DEL TTCT TTCT - TCGA-Y8-A8S1-01A-11D-A36X-10 TCGA-Y8-A8S1-10A-01D-A370-10 g.chr3:69097304_69097307delTTCT c.549_552delAGAA c.(547-552)aaagaafs p.KE183fs KIRP 3 69101211 69101211 + Silent SNP G G A TCGA-BQ-5878-01A-11D-1589-08 TCGA-BQ-5878-11A-01D-1589-08 g.chr3:69101211G>A c.27C>T c.(25-27)ctC>ctT p.L9L LGG 3 69075205 69075205 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:69075205C>T c.2801G>A c.(2800-2802)cGc>cAc p.R934H LGG 3 69079032 69079032 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:69079032C>T c.2528G>A c.(2527-2529)aGt>aAt p.S843N LGG 3 69088055 69088055 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:69088055C>A c.1933G>T c.(1933-1935)Gac>Tac p.D645Y LIHC 3 69079080 69079080 + Missense_Mutation SNP T T C TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr3:69079080T>C c.2480A>G c.(2479-2481)cAg>cGg p.Q827R LIHC 3 69084229 69084229 + Missense_Mutation SNP T T A TCGA-DD-AADF-01A-11D-A40R-10 TCGA-DD-AADF-10A-01D-A40U-10 g.chr3:69084229T>A c.2189A>T c.(2188-2190)cAa>cTa p.Q730L LIHC 3 69084238 69084238 + Missense_Mutation SNP C C A TCGA-EP-A3JL-01A-11D-A20W-10 TCGA-EP-A3JL-10A-01D-A20W-10 g.chr3:69084238C>A c.2180G>T c.(2179-2181)cGt>cTt p.R727L LIHC 3 69097054 69097054 + Missense_Mutation SNP T T C TCGA-CC-A7IH-01A-11D-A33K-10 TCGA-CC-A7IH-10A-01D-A33K-10 g.chr3:69097054T>C c.802A>G c.(802-804)Ata>Gta p.I268V LIHC 3 69097137 69097137 + Missense_Mutation SNP T T C TCGA-CC-A3MC-01A-11D-A22F-10 TCGA-CC-A3MC-10A-01D-A22F-10 g.chr3:69097137T>C c.719A>G c.(718-720)aAt>aGt p.N240S LIHC 3 69101099 69101099 + Missense_Mutation SNP G G A TCGA-G3-AAV6-01A-21D-A36X-10 TCGA-G3-AAV6-10A-01D-A370-10 g.chr3:69101099G>A c.139C>T c.(139-141)Ccg>Tcg p.P47S LUAD 3 69073259 69073259 + Missense_Mutation SNP C C T TCGA-49-6745-01A-11D-1855-08 TCGA-49-6745-11A-01D-1855-08 g.chr3:69073259C>T c.3085G>A c.(3085-3087)Gat>Aat p.D1029N LUAD 3 69077407 69077407 + Silent SNP T T A TCGA-97-7938-01A-11D-2167-08 TCGA-97-7938-10A-01D-2167-08 g.chr3:69077407T>A c.2634A>T c.(2632-2634)gtA>gtT p.V878V LUAD 3 69078995 69078995 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr3:69078995C>A c.2565G>T c.(2563-2565)agG>agT p.R855S LUAD 3 69079029 69079029 + Missense_Mutation SNP C C A TCGA-50-5045-01A-01D-1625-08 TCGA-50-5045-10A-01D-1625-08 g.chr3:69079029C>A c.2531G>T c.(2530-2532)aGa>aTa p.R844I LUAD 3 69082733 69082733 + Missense_Mutation SNP C C A TCGA-44-7661-01A-11D-2063-08 TCGA-44-7661-11A-01D-2063-08 g.chr3:69082733C>A c.2367G>T c.(2365-2367)tgG>tgT p.W789C LUAD 3 69084217 69084217 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr3:69084217C>A c.2201G>T c.(2200-2202)aGa>aTa p.R734I LUAD 3 69087813 69087813 + Missense_Mutation SNP C C A TCGA-17-Z010-01A-01W-0746-08 TCGA-17-Z010-11A-01W-0746-08 g.chr3:69087813C>A c.2053G>T c.(2053-2055)Gct>Tct p.A685S LUAD 3 69097192 69097192 + Missense_Mutation SNP T T C TCGA-50-6592-01A-11D-1753-08 TCGA-50-6592-11A-01D-1753-08 g.chr3:69097192T>C c.664A>G c.(664-666)Aca>Gca p.T222A LUAD 3 69097285 69097285 + Missense_Mutation SNP T T C TCGA-17-Z044-01A-01W-0746-08 TCGA-17-Z044-11A-01W-0746-08 g.chr3:69097285T>C c.571A>G c.(571-573)Act>Gct p.T191A LUAD 3 69097684 69097684 + Missense_Mutation SNP C C G TCGA-78-7149-01A-11D-2036-08 TCGA-78-7149-10A-01D-2036-08 g.chr3:69097684C>G c.172G>C c.(172-174)Gat>Cat p.D58H LUSC 3 69072406 69072406 + Silent SNP T T C TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr3:69072406T>C c.3204A>G c.(3202-3204)gaA>gaG p.E1068E LUSC 3 69075232 69075232 + Missense_Mutation SNP G G T TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr3:69075232G>T c.2774C>A c.(2773-2775)tCt>tAt p.S925Y LUSC 3 69097101 69097101 + Missense_Mutation SNP C C A TCGA-60-2709-01A-21D-1817-08 TCGA-60-2709-11A-01D-1817-08 g.chr3:69097101C>A c.755G>T c.(754-756)gGt>gTt p.G252V LUSC 3 69097222 69097222 + Missense_Mutation SNP T T A TCGA-39-5016-01A-01D-1441-08 TCGA-39-5016-11A-01D-1441-08 g.chr3:69097222T>A c.634A>T c.(634-636)Aat>Tat p.N212Y LUSC 3 69101202 69101202 + Silent SNP G G A TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr3:69101202G>A c.36C>T c.(34-36)ttC>ttT p.F12F OV 3 69082855 69082856 + Splice_Site DNP TC TC GA TCGA-24-1563-01A-01W-0553-09 TCGA-24-1563-10A-01W-0553-09 g.chr3:69082855_69082856TC>GA c.2245_2245GA>TC c.(2245-2247)GAag>TCaag p.E749S PAAD 3 69073265 69073265 + Missense_Mutation SNP G G T TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr3:69073265G>T c.3079C>A c.(3079-3081)Caa>Aaa p.Q1027K PAAD 3 69082709 69082710 + Frame_Shift_Del DEL AG AG - TCGA-2J-AAB4-01A-12D-A40W-08 TCGA-2J-AAB4-10A-01D-A40W-08 g.chr3:69082709_69082710delAG c.2390_2391delCT c.(2389-2391)tctfs p.S797fs PAAD 3 69087861 69087861 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:69087861C>A c.2005G>T c.(2005-2007)Gat>Tat p.D669Y PRAD 3 69075248 69075248 + Splice_Site SNP C C A TCGA-EJ-7788-01A-11D-2114-08 TCGA-EJ-7788-10A-01D-2114-08 g.chr3:69075248C>A c.2758G>T c.(2758-2760)Gaa>Taa p.E920* PRAD 3 69087802 69087802 + Silent SNP A A C TCGA-VN-A88P-01A-11D-A34U-08 TCGA-VN-A88P-10A-01D-A34X-08 g.chr3:69087802A>C c.2064T>G c.(2062-2064)cgT>cgG p.R688R PRAD 3 69097585 69097585 + Missense_Mutation SNP C C T TCGA-J4-A67O-01A-11D-A30E-08 TCGA-J4-A67O-10A-01D-A30H-08 g.chr3:69097585C>T c.271G>A c.(271-273)Gat>Aat p.D91N READ 3 69096730 69096730 + Missense_Mutation SNP T T C TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr3:69096730T>C c.1126A>G c.(1126-1128)Aaa>Gaa p.K376E SKCM 3 69079079 69079079 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr3:69079079C>T c.2481G>A c.(2479-2481)caG>caA p.Q827Q SKCM 3 69079119 69079120 + Frame_Shift_Del DEL TC TC - TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr3:69079119_69079120delTC c.2440_2441delGA c.(2440-2442)gaafs p.E814fs SKCM 3 69088085 69088085 + Nonsense_Mutation SNP G G A TCGA-D3-A1QB-06A-11D-A19A-08 TCGA-D3-A1QB-10A-01D-A19A-08 g.chr3:69088085G>A c.1903C>T c.(1903-1905)Caa>Taa p.Q635* SKCM 3 69092038 69092038 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:69092038A>C c.1604T>G c.(1603-1605)cTt>cGt p.L535R SKCM 3 69092986 69092986 + Missense_Mutation SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr3:69092986G>A c.1493C>T c.(1492-1494)tCc>tTc p.S498F SKCM 3 69096510 69096510 + Splice_Site SNP T T A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:69096510T>A c.1346A>T c.(1345-1347)aAg>aTg p.K449M SKCM 3 69097377 69097377 + Missense_Mutation SNP G G A TCGA-FW-A5DY-06A-11D-A30X-08 TCGA-FW-A5DY-11A-12D-A30X-08 g.chr3:69097377G>A c.479C>T c.(478-480)tCa>tTa p.S160L SKCM 3 69097533 69097533 + Missense_Mutation SNP G G A TCGA-EE-A29W-06A-11D-A196-08 TCGA-EE-A29W-10A-01D-A198-08 g.chr3:69097533G>A c.323C>T c.(322-324)aCc>aTc p.T108I SKCM 3 69097638 69097638 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr3:69097638G>A c.218C>T c.(217-219)cCa>cTa p.P73L SKCM 3 69097669 69097669 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr3:69097669C>T c.187G>A c.(187-189)Ggg>Agg p.G63R

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 69073247 69073247 single base substitution C T 3_prime_UTR_variant BLCA-CN 3 69073247 69073247 single base substitution C T downstream_gene_variant BLCA-CN 3 69073247 69073247 single base substitution C T missense_variant E1033K 3097G>A BLCA-CN 3 69073247 69073247 single base substitution C T missense_variant E1036K 3106G>A BLCA-CN 3 69077411 69077411 single base substitution T C 3_prime_UTR_variant BLCA-CN 3 69077411 69077411 single base substitution T C missense_variant Y877C 2630A>G BLCA-CN 3 69077411 69077411 single base substitution T C missense_variant Y880C 2639A>G BLCA-CN 3 69077411 69077411 single base substitution T C upstream_gene_variant BLCA-CN 3 69079039 69079039 single base substitution C G 3_prime_UTR_variant BLCA-CN 3 69079039 69079039 single base substitution C G missense_variant E841Q 2521G>C BLCA-CN 3 69079039 69079039 single base substitution C G missense_variant E844Q 2530G>C BLCA-CN 3 69079039 69079039 single base substitution C G upstream_gene_variant BLCA-CN 3 69097538 69097538 single base substitution G C exon_variant BLCA-CN 3 69097538 69097538 single base substitution G C synonymous_variant V106V 318C>G BLCA-CN 3 69097538 69097538 single base substitution G C upstream_gene_variant BLCA-CN 3 69105200 69105200 single base substitution G A upstream_gene_variant BLCA-US 3 69074854 69074854 single base substitution G A 3_prime_UTR_variant BLCA-US 3 69074854 69074854 single base substitution G A exon_variant BLCA-US 3 69074854 69074854 single base substitution G A missense_variant H957Y 2869C>T BLCA-US 3 69074854 69074854 single base substitution G A missense_variant H960Y 2878C>T BLCA-US 3 69097297 69097297 single base substitution T C exon_variant BLCA-US 3 69097297 69097297 single base substitution T C missense_variant M187V 559A>G BLCA-US 3 69097297 69097297 single base substitution T C upstream_gene_variant BRCA-EU 3 69067827 69067827 single base substitution T G downstream_gene_variant BRCA-EU 3 69068173 69068173 single base substitution G C downstream_gene_variant BRCA-EU 3 69071098 69071098 single base substitution G A 3_prime_UTR_variant BRCA-EU 3 69071098 69071098 single base substitution G A downstream_gene_variant BRCA-EU 3 69071952 69071953 deletion of <=200bp AT - 3_prime_UTR_variant BRCA-EU 3 69071952 69071953 deletion of <=200bp AT - downstream_gene_variant BRCA-EU 3 69080976 69080976 single base substitution C T intron_variant BRCA-EU 3 69083699 69083699 single base substitution G A intron_variant BRCA-EU 3 69084347 69084347 single base substitution G A intron_variant BRCA-EU 3 69086302 69086302 single base substitution A C intron_variant BRCA-EU 3 69089586 69089586 single base substitution G T downstream_gene_variant BRCA-EU 3 69089586 69089586 single base substitution G T intron_variant BRCA-EU 3 69089679 69089679 single base substitution G A downstream_gene_variant BRCA-EU 3 69089679 69089679 single base substitution G A intron_variant BRCA-EU 3 69090485 69090485 single base substitution T G downstream_gene_variant BRCA-EU 3 69090485 69090485 single base substitution T G intron_variant BRCA-EU 3 69091849 69091849 single base substitution A G downstream_gene_variant BRCA-EU 3 69091849 69091849 single base substitution A G intron_variant BRCA-EU 3 69095208 69095208 single base substitution C T intron_variant BRCA-EU 3 69095208 69095208 single base substitution C T upstream_gene_variant BRCA-EU 3 69097264 69097264 single base substitution C T exon_variant BRCA-EU 3 69097264 69097264 single base substitution C T missense_variant E198K 592G>A BRCA-EU 3 69097264 69097264 single base substitution C T upstream_gene_variant BRCA-EU 3 69098354 69098354 single base substitution C A intron_variant BRCA-EU 3 69098354 69098354 single base substitution C A upstream_gene_variant BRCA-EU 3 69098766 69098766 deletion of <=200bp T - intron_variant BRCA-EU 3 69098766 69098766 deletion of <=200bp T - upstream_gene_variant BRCA-EU 3 69100005 69100005 single base substitution T G intron_variant BRCA-EU 3 69101934 69101936 deletion of <=200bp TAG - upstream_gene_variant BRCA-EU 3 69102280 69102280 single base substitution A T upstream_gene_variant BRCA-EU 3 69104152 69104152 single base substitution A G upstream_gene_variant BRCA-EU 3 69105324 69105324 single base substitution C T upstream_gene_variant BRCA-FR 3 69089992 69089992 single base substitution G A downstream_gene_variant BRCA-FR 3 69089992 69089992 single base substitution G A intron_variant BRCA-FR 3 69097264 69097264 single base substitution C T exon_variant BRCA-FR 3 69097264 69097264 single base substitution C T missense_variant E198K 592G>A BRCA-FR 3 69097264 69097264 single base substitution C T upstream_gene_variant BRCA-UK 3 69066725 69066725 single base substitution G A downstream_gene_variant BRCA-UK 3 69067115 69067115 single base substitution G C downstream_gene_variant BRCA-UK 3 69099815 69099815 single base substitution G C intron_variant BRCA-UK 3 69100005 69100005 single base substitution T G intron_variant BRCA-US 3 69072340 69072340 single base substitution T C 3_prime_UTR_variant BRCA-US 3 69072340 69072340 single base substitution T C downstream_gene_variant BRCA-US 3 69072340 69072340 single base substitution T C synonymous_variant Q1090Q 3270A>G BRCA-US 3 69072340 69072340 single base substitution T C synonymous_variant Q1093Q 3279A>G BRCA-US 3 69084265 69084265 single base substitution A C missense_variant V718G 2153T>G BRCA-US 3 69084265 69084265 single base substitution A C missense_variant V721G 2162T>G BRCA-US 3 69084265 69084265 single base substitution A C splice_region_variant BRCA-US 3 69088027 69088027 single base substitution C T downstream_gene_variant BRCA-US 3 69088027 69088027 single base substitution C T exon_variant BRCA-US 3 69088027 69088027 single base substitution C T missense_variant R654Q 1961G>A BRCA-US 3 69088027 69088027 single base substitution C T missense_variant R657Q 1970G>A BRCA-US 3 69096739 69096739 single base substitution C T exon_variant BRCA-US 3 69096739 69096739 single base substitution C T missense_variant A373T 1117G>A BRCA-US 3 69096739 69096739 single base substitution C T upstream_gene_variant BRCA-US 3 69097500 69097500 single base substitution G A exon_variant BRCA-US 3 69097500 69097500 single base substitution G A missense_variant P119L 356C>T BRCA-US 3 69097500 69097500 single base substitution G A upstream_gene_variant BTCA-JP 3 69073434 69073434 single base substitution T G exon_variant BTCA-JP 3 69073434 69073434 single base substitution T G intron_variant BTCA-JP 3 69077468 69077468 insertion of <=200bp - A intron_variant BTCA-JP 3 69077468 69077468 insertion of <=200bp - A upstream_gene_variant BTCA-JP 3 69079174 69079174 deletion of <=200bp A - intron_variant BTCA-JP 3 69079174 69079174 deletion of <=200bp A - upstream_gene_variant BTCA-JP 3 69101257 69101257 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BTCA-JP 3 69104492 69104492 single base substitution G A upstream_gene_variant BTCA-JP 3 69105757 69105757 single base substitution A G upstream_gene_variant CESC-US 3 69066043 69066043 single base substitution G T downstream_gene_variant CESC-US 3 69073265 69073265 single base substitution G C 3_prime_UTR_variant CESC-US 3 69073265 69073265 single base substitution G C downstream_gene_variant CESC-US 3 69073265 69073265 single base substitution G C missense_variant Q1027E 3079C>G CESC-US 3 69073265 69073265 single base substitution G C missense_variant Q1030E 3088C>G CESC-US 3 69075149 69075149 single base substitution G C missense_variant Q953E 2857C>G CESC-US 3 69075149 69075149 single base substitution G C missense_variant Q956E 2866C>G CESC-US 3 69075149 69075149 single base substitution G C splice_region_variant CESC-US 3 69093647 69093647 single base substitution T G exon_variant CESC-US 3 69093647 69093647 single base substitution T G missense_variant K483Q 1447A>C CESC-US 3 69093647 69093647 single base substitution T G missense_variant K486Q 1456A>C CESC-US 3 69098114 69098114 single base substitution G A intron_variant CESC-US 3 69098114 69098114 single base substitution G A upstream_gene_variant CESC-US 3 69101209 69101209 single base substitution G C exon_variant CESC-US 3 69101209 69101209 single base substitution G C missense_variant S10C 29C>G COAD-US 3 69072455 69072455 single base substitution T C 3_prime_UTR_variant COAD-US 3 69072455 69072455 single base substitution T C downstream_gene_variant COAD-US 3 69072455 69072455 single base substitution T C missense_variant Y1052C 3155A>G COAD-US 3 69072455 69072455 single base substitution T C missense_variant Y1055C 3164A>G COAD-US 3 69074743 69074743 single base substitution T A 3_prime_UTR_variant COAD-US 3 69074743 69074743 single base substitution T A exon_variant COAD-US 3 69074743 69074743 single base substitution T A stop_gained K994* 2980A>T COAD-US 3 69074743 69074743 single base substitution T A stop_gained K997* 2989A>T COAD-US 3 69074854 69074854 single base substitution G A 3_prime_UTR_variant COAD-US 3 69074854 69074854 single base substitution G A exon_variant COAD-US 3 69074854 69074854 single base substitution G A missense_variant H957Y 2869C>T COAD-US 3 69074854 69074854 single base substitution G A missense_variant H960Y 2878C>T COAD-US 3 69077112 69077112 single base substitution C A 3_prime_UTR_variant COAD-US 3 69077112 69077112 single base substitution C A missense_variant R899I 2696G>T COAD-US 3 69077112 69077112 single base substitution C A missense_variant R902I 2705G>T COAD-US 3 69077112 69077112 single base substitution C A upstream_gene_variant COAD-US 3 69082708 69082708 single base substitution C G intron_variant COAD-US 3 69082708 69082708 single base substitution C G missense_variant D798H 2392G>C COAD-US 3 69082708 69082708 single base substitution C G missense_variant D801H 2401G>C COAD-US 3 69084177 69084177 single base substitution C T exon_variant COAD-US 3 69084177 69084177 single base substitution C T synonymous_variant Q747Q 2241G>A COAD-US 3 69084177 69084177 single base substitution C T synonymous_variant Q750Q 2250G>A COAD-US 3 69088067 69088067 single base substitution G A downstream_gene_variant COAD-US 3 69088067 69088067 single base substitution G A exon_variant COAD-US 3 69088067 69088067 single base substitution G A missense_variant R641C 1921C>T COAD-US 3 69088067 69088067 single base substitution G A missense_variant R644C 1930C>T COAD-US 3 69088121 69088121 single base substitution C A downstream_gene_variant COAD-US 3 69088121 69088121 single base substitution C A exon_variant COAD-US 3 69088121 69088121 single base substitution C A stop_gained E623* 1867G>T COAD-US 3 69088121 69088121 single base substitution C A stop_gained E626* 1876G>T COAD-US 3 69088715 69088715 single base substitution T C downstream_gene_variant COAD-US 3 69088715 69088715 single base substitution T C exon_variant COAD-US 3 69088715 69088715 single base substitution T C missense_variant Q605R 1814A>G COAD-US 3 69088715 69088715 single base substitution T C missense_variant Q608R 1823A>G COAD-US 3 69088798 69088798 single base substitution C A downstream_gene_variant COAD-US 3 69088798 69088798 single base substitution C A exon_variant COAD-US 3 69088798 69088798 single base substitution C A missense_variant K577N 1731G>T COAD-US 3 69088798 69088798 single base substitution C A missense_variant K580N 1740G>T COAD-US 3 69096775 69096775 single base substitution T G exon_variant COAD-US 3 69096775 69096775 single base substitution T G missense_variant N361H 1081A>C COAD-US 3 69096775 69096775 single base substitution T G upstream_gene_variant COAD-US 3 69097150 69097150 single base substitution C A exon_variant COAD-US 3 69097150 69097150 single base substitution C A missense_variant D236Y 706G>T COAD-US 3 69097150 69097150 single base substitution C A upstream_gene_variant COAD-US 3 69097670 69097670 single base substitution C T exon_variant COAD-US 3 69097670 69097670 single base substitution C T stop_gained W62* 186G>A COAD-US 3 69097670 69097670 single base substitution C T upstream_gene_variant COAD-US 3 69105054 69105054 single base substitution C T upstream_gene_variant COAD-US 3 69105055 69105055 single base substitution G A upstream_gene_variant COAD-US 3 69105826 69105826 single base substitution A G upstream_gene_variant COCA-CN 3 69075111 69075111 single base substitution C A intron_variant COCA-CN 3 69075273 69075273 single base substitution T C intron_variant COCA-CN 3 69075273 69075273 single base substitution T C upstream_gene_variant COCA-CN 3 69078887 69078887 single base substitution C T intron_variant COCA-CN 3 69078887 69078887 single base substitution C T upstream_gene_variant COCA-CN 3 69079184 69079184 single base substitution C A intron_variant COCA-CN 3 69079184 69079184 single base substitution C A upstream_gene_variant COCA-CN 3 69084062 69084062 single base substitution G C intron_variant COCA-CN 3 69087786 69087786 single base substitution C A exon_variant COCA-CN 3 69087786 69087786 single base substitution C A stop_gained E694* 2080G>T COCA-CN 3 69087786 69087786 single base substitution C A stop_gained E697* 2089G>T COCA-CN 3 69091777 69091777 single base substitution T C downstream_gene_variant COCA-CN 3 69091777 69091777 single base substitution T C intron_variant COCA-CN 3 69096493 69096493 single base substitution C A intron_variant COCA-CN 3 69096493 69096493 single base substitution C A splice_region_variant COCA-CN 3 69096493 69096493 single base substitution C A upstream_gene_variant COCA-CN 3 69096516 69096516 single base substitution A G exon_variant COCA-CN 3 69096516 69096516 single base substitution A G missense_variant V447A 1340T>C COCA-CN 3 69096516 69096516 single base substitution A G upstream_gene_variant COCA-CN 3 69097116 69097116 single base substitution C A exon_variant COCA-CN 3 69097116 69097116 single base substitution C A missense_variant S247I 740G>T COCA-CN 3 69097116 69097116 single base substitution C A upstream_gene_variant COCA-CN 3 69097428 69097428 single base substitution C A exon_variant COCA-CN 3 69097428 69097428 single base substitution C A missense_variant R143I 428G>T COCA-CN 3 69097428 69097428 single base substitution C A upstream_gene_variant COCA-CN 3 69100978 69100978 single base substitution A G intron_variant COCA-CN 3 69104520 69104520 single base substitution C T upstream_gene_variant COCA-CN 3 69105076 69105076 single base substitution T C upstream_gene_variant COCA-CN 3 69105131 69105131 single base substitution T G upstream_gene_variant COCA-CN 3 69106304 69106304 single base substitution C T upstream_gene_variant COCA-CN 3 69106305 69106305 single base substitution C G upstream_gene_variant EOPC-DE 3 69073436 69073436 single base substitution G T exon_variant EOPC-DE 3 69073436 69073436 single base substitution G T intron_variant EOPC-DE 3 69092376 69092376 single base substitution A T downstream_gene_variant EOPC-DE 3 69092376 69092376 single base substitution A T intron_variant ESAD-UK 3 69071650 69071650 single base substitution A G 3_prime_UTR_variant ESAD-UK 3 69071650 69071650 single base substitution A G downstream_gene_variant ESAD-UK 3 69072206 69072206 single base substitution T A 3_prime_UTR_variant ESAD-UK 3 69072206 69072206 single base substitution T A downstream_gene_variant ESAD-UK 3 69072704 69072704 single base substitution A C downstream_gene_variant ESAD-UK 3 69072704 69072704 single base substitution A C intron_variant ESAD-UK 3 69072743 69072743 single base substitution A T downstream_gene_variant ESAD-UK 3 69072743 69072743 single base substitution A T intron_variant ESAD-UK 3 69073035 69073039 deletion of <=200bp ATGTA - downstream_gene_variant ESAD-UK 3 69073035 69073039 deletion of <=200bp ATGTA - intron_variant ESAD-UK 3 69075008 69075008 single base substitution A G intron_variant ESAD-UK 3 69075259 69075259 deletion of <=200bp A - intron_variant ESAD-UK 3 69075259 69075259 deletion of <=200bp A - upstream_gene_variant ESAD-UK 3 69075507 69075507 single base substitution G A intron_variant ESAD-UK 3 69075507 69075507 single base substitution G A upstream_gene_variant ESAD-UK 3 69077781 69077781 single base substitution G T intron_variant ESAD-UK 3 69077781 69077781 single base substitution G T upstream_gene_variant ESAD-UK 3 69077791 69077791 single base substitution C T intron_variant ESAD-UK 3 69077791 69077791 single base substitution C T upstream_gene_variant ESAD-UK 3 69079574 69079574 single base substitution T C intron_variant ESAD-UK 3 69079574 69079574 single base substitution T C upstream_gene_variant ESAD-UK 3 69079905 69079905 single base substitution G C intron_variant ESAD-UK 3 69079905 69079905 single base substitution G C upstream_gene_variant ESAD-UK 3 69081414 69081414 insertion of <=200bp - C intron_variant ESAD-UK 3 69081420 69081420 single base substitution C T intron_variant ESAD-UK 3 69086125 69086125 single base substitution G A intron_variant ESAD-UK 3 69086615 69086615 single base substitution G T intron_variant ESAD-UK 3 69092265 69092265 single base substitution T C downstream_gene_variant ESAD-UK 3 69092265 69092265 single base substitution T C intron_variant ESAD-UK 3 69095113 69095113 single base substitution G A intron_variant ESAD-UK 3 69095113 69095113 single base substitution G A upstream_gene_variant ESAD-UK 3 69096395 69096395 single base substitution C T intron_variant ESAD-UK 3 69096395 69096395 single base substitution C T upstream_gene_variant ESAD-UK 3 69097608 69097608 single base substitution T C exon_variant ESAD-UK 3 69097608 69097608 single base substitution T C missense_variant K83R 248A>G ESAD-UK 3 69097608 69097608 single base substitution T C upstream_gene_variant ESAD-UK 3 69098790 69098790 single base substitution G C intron_variant ESAD-UK 3 69101307 69101307 single base substitution A G 5_prime_UTR_variant ESAD-UK 3 69102833 69102833 single base substitution C G upstream_gene_variant ESCA-CN 3 69077090 69077090 single base substitution C T 3_prime_UTR_variant ESCA-CN 3 69077090 69077090 single base substitution C T synonymous_variant R906R 2718G>A ESCA-CN 3 69077090 69077090 single base substitution C T synonymous_variant R909R 2727G>A ESCA-CN 3 69077090 69077090 single base substitution C T upstream_gene_variant ESCA-CN 3 69093668 69093668 single base substitution C A exon_variant ESCA-CN 3 69093668 69093668 single base substitution C A stop_gained E476* 1426G>T ESCA-CN 3 69093668 69093668 single base substitution C A stop_gained E479* 1435G>T GBM-US 3 69075241 69075241 single base substitution T C 3_prime_UTR_variant GBM-US 3 69075241 69075241 single base substitution T C exon_variant GBM-US 3 69075241 69075241 single base substitution T C missense_variant K922R 2765A>G GBM-US 3 69075241 69075241 single base substitution T C missense_variant K925R 2774A>G GBM-US 3 69097037 69097037 single base substitution C T exon_variant GBM-US 3 69097037 69097037 single base substitution C T synonymous_variant A273A 819G>A GBM-US 3 69097037 69097037 single base substitution C T upstream_gene_variant GBM-US 3 69097485 69097485 single base substitution C T exon_variant GBM-US 3 69097485 69097485 single base substitution C T missense_variant R124Q 371G>A GBM-US 3 69097485 69097485 single base substitution C T upstream_gene_variant KIRC-US 3 69073260 69073260 single base substitution A C 3_prime_UTR_variant KIRC-US 3 69073260 69073260 single base substitution A C downstream_gene_variant KIRC-US 3 69073260 69073260 single base substitution A C missense_variant N1028K 3084T>G KIRC-US 3 69073260 69073260 single base substitution A C missense_variant N1031K 3093T>G KIRP-US 3 69072460 69072460 single base substitution T C 3_prime_UTR_variant KIRP-US 3 69072460 69072460 single base substitution T C downstream_gene_variant KIRP-US 3 69072460 69072460 single base substitution T C synonymous_variant Q1050Q 3150A>G KIRP-US 3 69072460 69072460 single base substitution T C synonymous_variant Q1053Q 3159A>G KIRP-US 3 69096768 69096770 deletion of <=200bp GAA - disruptive_inframe_deletion SS362S KIRP-US 3 69096768 69096770 deletion of <=200bp GAA - exon_variant KIRP-US 3 69096768 69096770 deletion of <=200bp GAA - upstream_gene_variant KIRP-US 3 69101211 69101211 single base substitution G A exon_variant KIRP-US 3 69101211 69101211 single base substitution G A synonymous_variant L9L 27C>T LAML-KR 3 69065410 69065410 single base substitution G T downstream_gene_variant LAML-KR 3 69074930 69074930 single base substitution G A intron_variant LAML-KR 3 69084009 69084009 single base substitution A G intron_variant LICA-CN 3 69101134 69101134 single base substitution G C exon_variant LICA-CN 3 69101134 69101134 single base substitution G C missense_variant P35R 104C>G LICA-FR 3 69082425 69082426 deletion of <=200bp AA - intron_variant LICA-FR 3 69097217 69097217 single base substitution C A exon_variant LICA-FR 3 69097217 69097217 single base substitution C A synonymous_variant T213T 639G>T LICA-FR 3 69097217 69097217 single base substitution C A upstream_gene_variant LICA-FR 3 69105965 69105965 single base substitution A G upstream_gene_variant LIHC-US 3 69079080 69079080 single base substitution T C exon_variant LIHC-US 3 69079080 69079080 single base substitution T C missense_variant Q827R 2480A>G LIHC-US 3 69079080 69079080 single base substitution T C missense_variant Q830R 2489A>G LIHC-US 3 69079080 69079080 single base substitution T C upstream_gene_variant LIHC-US 3 69084238 69084238 single base substitution C A exon_variant LIHC-US 3 69084238 69084238 single base substitution C A missense_variant R727L 2180G>T LIHC-US 3 69084238 69084238 single base substitution C A missense_variant R730L 2189G>T LIHC-US 3 69097054 69097054 single base substitution T C exon_variant LIHC-US 3 69097054 69097054 single base substitution T C missense_variant I268V 802A>G LIHC-US 3 69097054 69097054 single base substitution T C upstream_gene_variant LIHC-US 3 69097137 69097137 single base substitution T C exon_variant LIHC-US 3 69097137 69097137 single base substitution T C missense_variant N240S 719A>G LIHC-US 3 69097137 69097137 single base substitution T C upstream_gene_variant LINC-JP 3 69068846 69068846 single base substitution T C downstream_gene_variant LINC-JP 3 69073420 69073421 deletion of <=200bp TT - downstream_gene_variant LINC-JP 3 69073420 69073421 deletion of <=200bp TT - intron_variant LINC-JP 3 69075267 69075267 single base substitution T A intron_variant LINC-JP 3 69075267 69075267 single base substitution T A upstream_gene_variant LINC-JP 3 69077523 69077523 single base substitution T C intron_variant LINC-JP 3 69077523 69077523 single base substitution T C upstream_gene_variant LINC-JP 3 69081529 69081529 single base substitution T C intron_variant LINC-JP 3 69085728 69085728 single base substitution C T intron_variant LINC-JP 3 69092789 69092789 single base substitution T C downstream_gene_variant LINC-JP 3 69092789 69092789 single base substitution T C intron_variant LINC-JP 3 69100368 69100368 single base substitution C G intron_variant LINC-JP 3 69104554 69104554 single base substitution T C upstream_gene_variant LINC-JP 3 69105051 69105051 single base substitution T C upstream_gene_variant LIRI-JP 3 69065724 69065724 single base substitution G A downstream_gene_variant LIRI-JP 3 69066232 69066232 single base substitution C T downstream_gene_variant LIRI-JP 3 69066273 69066273 single base substitution A T downstream_gene_variant LIRI-JP 3 69066407 69066407 single base substitution G T downstream_gene_variant LIRI-JP 3 69069742 69069742 single base substitution T G 3_prime_UTR_variant LIRI-JP 3 69069742 69069742 single base substitution T G downstream_gene_variant LIRI-JP 3 69071860 69071860 single base substitution T C 3_prime_UTR_variant LIRI-JP 3 69071860 69071860 single base substitution T C downstream_gene_variant LIRI-JP 3 69072989 69072989 single base substitution T C downstream_gene_variant LIRI-JP 3 69072989 69072989 single base substitution T C intron_variant LIRI-JP 3 69075096 69075096 single base substitution T G intron_variant LIRI-JP 3 69075576 69075576 single base substitution C T intron_variant LIRI-JP 3 69075576 69075576 single base substitution C T upstream_gene_variant LIRI-JP 3 69079325 69079325 single base substitution T G intron_variant LIRI-JP 3 69079325 69079325 single base substitution T G upstream_gene_variant LIRI-JP 3 69083417 69083417 single base substitution A C intron_variant LIRI-JP 3 69083621 69083621 single base substitution C T intron_variant LIRI-JP 3 69084447 69084447 single base substitution A T intron_variant LIRI-JP 3 69085689 69085689 single base substitution T C intron_variant LIRI-JP 3 69087621 69087621 single base substitution C A intron_variant LIRI-JP 3 69090610 69090610 single base substitution T A downstream_gene_variant LIRI-JP 3 69090610 69090610 single base substitution T A intron_variant LIRI-JP 3 69090903 69090903 single base substitution T C downstream_gene_variant LIRI-JP 3 69090903 69090903 single base substitution T C intron_variant LIRI-JP 3 69091004 69091004 single base substitution T C downstream_gene_variant LIRI-JP 3 69091004 69091004 single base substitution T C intron_variant LIRI-JP 3 69091661 69091661 single base substitution T C downstream_gene_variant LIRI-JP 3 69091661 69091661 single base substitution T C intron_variant LIRI-JP 3 69091861 69091861 single base substitution T C downstream_gene_variant LIRI-JP 3 69091861 69091861 single base substitution T C intron_variant LIRI-JP 3 69092091 69092091 single base substitution G A downstream_gene_variant LIRI-JP 3 69092091 69092091 single base substitution G A intron_variant LIRI-JP 3 69092228 69092228 single base substitution A T downstream_gene_variant LIRI-JP 3 69092228 69092228 single base substitution A T intron_variant LIRI-JP 3 69092901 69092901 single base substitution C T downstream_gene_variant LIRI-JP 3 69092901 69092901 single base substitution C T splice_region_variant LIRI-JP 3 69095504 69095507 deletion of <=200bp TAAA - intron_variant LIRI-JP 3 69095504 69095507 deletion of <=200bp TAAA - upstream_gene_variant LIRI-JP 3 69096883 69096883 single base substitution T C exon_variant LIRI-JP 3 69096883 69096883 single base substitution T C missense_variant R325G 973A>G LIRI-JP 3 69096883 69096883 single base substitution T C upstream_gene_variant LIRI-JP 3 69098292 69098292 single base substitution T C intron_variant LIRI-JP 3 69098292 69098292 single base substitution T C upstream_gene_variant LIRI-JP 3 69099353 69099353 single base substitution G A intron_variant LIRI-JP 3 69103258 69103258 single base substitution T C upstream_gene_variant LIRI-JP 3 69104586 69104586 single base substitution C A upstream_gene_variant LUSC-KR 3 69064819 69064819 single base substitution G T downstream_gene_variant LUSC-KR 3 69065410 69065410 single base substitution G T downstream_gene_variant LUSC-KR 3 69070563 69070563 single base substitution A C 3_prime_UTR_variant LUSC-KR 3 69070563 69070563 single base substitution A C downstream_gene_variant LUSC-KR 3 69072256 69072256 single base substitution T C 3_prime_UTR_variant LUSC-KR 3 69072256 69072256 single base substitution T C downstream_gene_variant LUSC-KR 3 69072481 69072481 single base substitution G A downstream_gene_variant LUSC-KR 3 69072481 69072481 single base substitution G A intron_variant LUSC-KR 3 69082657 69082657 single base substitution T C intron_variant LUSC-KR 3 69090072 69090072 single base substitution C A downstream_gene_variant LUSC-KR 3 69090072 69090072 single base substitution C A intron_variant LUSC-KR 3 69092438 69092438 single base substitution A C downstream_gene_variant LUSC-KR 3 69092438 69092438 single base substitution A C intron_variant LUSC-KR 3 69104491 69104491 single base substitution C A upstream_gene_variant LUSC-US 3 69072406 69072406 single base substitution T C 3_prime_UTR_variant LUSC-US 3 69072406 69072406 single base substitution T C downstream_gene_variant LUSC-US 3 69072406 69072406 single base substitution T C synonymous_variant E1068E 3204A>G LUSC-US 3 69072406 69072406 single base substitution T C synonymous_variant E1071E 3213A>G LUSC-US 3 69075232 69075232 single base substitution G T 3_prime_UTR_variant LUSC-US 3 69075232 69075232 single base substitution G T exon_variant LUSC-US 3 69075232 69075232 single base substitution G T missense_variant S925Y 2774C>A LUSC-US 3 69075232 69075232 single base substitution G T missense_variant S928Y 2783C>A LUSC-US 3 69097101 69097101 single base substitution C A exon_variant LUSC-US 3 69097101 69097101 single base substitution C A missense_variant G252V 755G>T LUSC-US 3 69097101 69097101 single base substitution C A upstream_gene_variant LUSC-US 3 69097222 69097222 single base substitution T A exon_variant LUSC-US 3 69097222 69097222 single base substitution T A missense_variant N212Y 634A>T LUSC-US 3 69097222 69097222 single base substitution T A upstream_gene_variant LUSC-US 3 69101202 69101202 single base substitution G A exon_variant LUSC-US 3 69101202 69101202 single base substitution G A synonymous_variant F12F 36C>T LUSC-US 3 69105003 69105003 single base substitution T A upstream_gene_variant MALY-DE 3 69064359 69064359 insertion of <=200bp - T downstream_gene_variant MALY-DE 3 69065157 69065157 single base substitution C G downstream_gene_variant MALY-DE 3 69070197 69070197 single base substitution G A 3_prime_UTR_variant MALY-DE 3 69070197 69070197 single base substitution G A downstream_gene_variant MALY-DE 3 69071136 69071136 single base substitution T A 3_prime_UTR_variant MALY-DE 3 69071136 69071136 single base substitution T A downstream_gene_variant MALY-DE 3 69080411 69080411 single base substitution G A intron_variant MALY-DE 3 69084502 69084502 single base substitution T A intron_variant MALY-DE 3 69088407 69088407 single base substitution T C downstream_gene_variant MALY-DE 3 69088407 69088407 single base substitution T C intron_variant MALY-DE 3 69095945 69095945 single base substitution T G intron_variant MALY-DE 3 69095945 69095945 single base substitution T G upstream_gene_variant MALY-DE 3 69101530 69101530 single base substitution C T upstream_gene_variant MALY-DE 3 69104521 69104521 single base substitution G A upstream_gene_variant MELA-AU 3 69065436 69065436 single base substitution G A downstream_gene_variant MELA-AU 3 69065440 69065440 single base substitution G A downstream_gene_variant MELA-AU 3 69065702 69065702 single base substitution G A downstream_gene_variant MELA-AU 3 69066855 69066855 single base substitution T C downstream_gene_variant MELA-AU 3 69067491 69067491 single base substitution T C downstream_gene_variant MELA-AU 3 69070044 69070044 single base substitution C T 3_prime_UTR_variant MELA-AU 3 69070044 69070044 single base substitution C T downstream_gene_variant MELA-AU 3 69070056 69070056 single base substitution T C 3_prime_UTR_variant MELA-AU 3 69070056 69070056 single base substitution T C downstream_gene_variant MELA-AU 3 69070518 69070518 single base substitution T C 3_prime_UTR_variant MELA-AU 3 69070518 69070518 single base substitution T C downstream_gene_variant MELA-AU 3 69070647 69070647 single base substitution G A 3_prime_UTR_variant MELA-AU 3 69070647 69070647 single base substitution G A downstream_gene_variant MELA-AU 3 69070661 69070661 single base substitution T C 3_prime_UTR_variant MELA-AU 3 69070661 69070661 single base substitution T C downstream_gene_variant MELA-AU 3 69071374 69071374 single base substitution T A 3_prime_UTR_variant MELA-AU 3 69071374 69071374 single base substitution T A downstream_gene_variant MELA-AU 3 69072363 69072363 single base substitution G A 3_prime_UTR_variant MELA-AU 3 69072363 69072363 single base substitution G A downstream_gene_variant MELA-AU 3 69072363 69072363 single base substitution G A stop_gained Q1083* 3247C>T MELA-AU 3 69072363 69072363 single base substitution G A stop_gained Q1086* 3256C>T MELA-AU 3 69072646 69072646 single base substitution G A downstream_gene_variant MELA-AU 3 69072646 69072646 single base substitution G A intron_variant MELA-AU 3 69072785 69072785 single base substitution G A downstream_gene_variant MELA-AU 3 69072785 69072785 single base substitution G A intron_variant MELA-AU 3 69073191 69073191 single base substitution G A downstream_gene_variant MELA-AU 3 69073191 69073191 single base substitution G A intron_variant MELA-AU 3 69073293 69073293 single base substitution C T 3_prime_UTR_variant MELA-AU 3 69073293 69073293 single base substitution C T downstream_gene_variant MELA-AU 3 69073293 69073293 single base substitution C T missense_variant M1017I 3051G>A MELA-AU 3 69073293 69073293 single base substitution C T missense_variant M1020I 3060G>A MELA-AU 3 69073614 69073614 single base substitution G A intron_variant MELA-AU 3 69074388 69074388 single base substitution G A intron_variant MELA-AU 3 69075255 69075255 single base substitution G A splice_region_variant MELA-AU 3 69075255 69075255 single base substitution G A upstream_gene_variant MELA-AU 3 69075579 69075579 single base substitution C T intron_variant MELA-AU 3 69075579 69075579 single base substitution C T upstream_gene_variant MELA-AU 3 69077865 69077865 single base substitution G A intron_variant MELA-AU 3 69077865 69077865 single base substitution G A upstream_gene_variant MELA-AU 3 69078095 69078095 single base substitution A G intron_variant MELA-AU 3 69078095 69078095 single base substitution A G upstream_gene_variant MELA-AU 3 69078553 69078553 single base substitution G A intron_variant MELA-AU 3 69078553 69078553 single base substitution G A upstream_gene_variant MELA-AU 3 69078823 69078823 single base substitution C T intron_variant MELA-AU 3 69078823 69078823 single base substitution C T upstream_gene_variant MELA-AU 3 69079484 69079484 single base substitution G A intron_variant MELA-AU 3 69079484 69079484 single base substitution G A upstream_gene_variant MELA-AU 3 69080446 69080446 single base substitution G A intron_variant MELA-AU 3 69081669 69081669 single base substitution C T intron_variant MELA-AU 3 69081830 69081830 single base substitution C T intron_variant MELA-AU 3 69082468 69082468 single base substitution A C intron_variant MELA-AU 3 69082712 69082712 single base substitution A C intron_variant MELA-AU 3 69082712 69082712 single base substitution A C synonymous_variant L796L 2388T>G MELA-AU 3 69082712 69082712 single base substitution A C synonymous_variant L799L 2397T>G MELA-AU 3 69082808 69082808 single base substitution A T intron_variant MELA-AU 3 69082808 69082808 single base substitution A T synonymous_variant V764V 2292T>A MELA-AU 3 69082808 69082808 single base substitution A T synonymous_variant V767V 2301T>A MELA-AU 3 69083113 69083113 single base substitution C T intron_variant MELA-AU 3 69083551 69083551 single base substitution G A intron_variant MELA-AU 3 69083862 69083862 single base substitution G A intron_variant MELA-AU 3 69083987 69083987 single base substitution G A intron_variant MELA-AU 3 69084107 69084107 single base substitution G A intron_variant MELA-AU 3 69084254 69084254 single base substitution T G exon_variant MELA-AU 3 69084254 69084254 single base substitution T G synonymous_variant R722R 2164A>C MELA-AU 3 69084254 69084254 single base substitution T G synonymous_variant R725R 2173A>C MELA-AU 3 69084388 69084388 single base substitution G A intron_variant MELA-AU 3 69087205 69087205 single base substitution G A intron_variant MELA-AU 3 69087780 69087780 single base substitution G A exon_variant MELA-AU 3 69087780 69087780 single base substitution G A missense_variant L696F 2086C>T MELA-AU 3 69087780 69087780 single base substitution G A missense_variant L699F 2095C>T MELA-AU 3 69088107 69088107 insertion of <=200bp - T downstream_gene_variant MELA-AU 3 69088107 69088107 insertion of <=200bp - T exon_variant MELA-AU 3 69088107 69088107 insertion of <=200bp - T frameshift_variant K627K? MELA-AU 3 69088107 69088107 insertion of <=200bp - T frameshift_variant K630K? MELA-AU 3 69088168 69088168 single base substitution T C downstream_gene_variant MELA-AU 3 69088168 69088168 single base substitution T C splice_region_variant MELA-AU 3 69088891 69088891 single base substitution A G downstream_gene_variant MELA-AU 3 69088891 69088891 single base substitution A G intron_variant MELA-AU 3 69089551 69089551 single base substitution G A downstream_gene_variant MELA-AU 3 69089551 69089551 single base substitution G A intron_variant MELA-AU 3 69089839 69089839 single base substitution G A downstream_gene_variant MELA-AU 3 69089839 69089839 single base substitution G A intron_variant MELA-AU 3 69090201 69090201 single base substitution C T downstream_gene_variant MELA-AU 3 69090201 69090201 single base substitution C T intron_variant MELA-AU 3 69090267 69090267 single base substitution C T downstream_gene_variant MELA-AU 3 69090267 69090267 single base substitution C T intron_variant MELA-AU 3 69090285 69090285 single base substitution T C downstream_gene_variant MELA-AU 3 69090285 69090285 single base substitution T C intron_variant MELA-AU 3 69090569 69090569 single base substitution G A downstream_gene_variant MELA-AU 3 69090569 69090569 single base substitution G A intron_variant MELA-AU 3 69090690 69090690 single base substitution C G downstream_gene_variant MELA-AU 3 69090690 69090690 single base substitution C G intron_variant MELA-AU 3 69090914 69090914 single base substitution A G downstream_gene_variant MELA-AU 3 69090914 69090914 single base substitution A G intron_variant MELA-AU 3 69090930 69090930 single base substitution A G downstream_gene_variant MELA-AU 3 69090930 69090930 single base substitution A G intron_variant MELA-AU 3 69093146 69093146 single base substitution A G intron_variant MELA-AU 3 69093183 69093183 single base substitution G A intron_variant MELA-AU 3 69093417 69093417 single base substitution G A intron_variant MELA-AU 3 69094099 69094099 single base substitution G A intron_variant MELA-AU 3 69094099 69094099 single base substitution G A upstream_gene_variant MELA-AU 3 69094201 69094201 single base substitution G A intron_variant MELA-AU 3 69094201 69094201 single base substitution G A upstream_gene_variant MELA-AU 3 69094619 69094619 single base substitution A G intron_variant MELA-AU 3 69094619 69094619 single base substitution A G upstream_gene_variant MELA-AU 3 69095454 69095454 single base substitution T A intron_variant MELA-AU 3 69095454 69095454 single base substitution T A upstream_gene_variant MELA-AU 3 69096236 69096236 single base substitution G A intron_variant MELA-AU 3 69096236 69096236 single base substitution G A upstream_gene_variant MELA-AU 3 69096392 69096392 single base substitution A G intron_variant MELA-AU 3 69096392 69096392 single base substitution A G upstream_gene_variant MELA-AU 3 69096414 69096414 single base substitution A G intron_variant MELA-AU 3 69096414 69096414 single base substitution A G upstream_gene_variant MELA-AU 3 69097302 69097302 single base substitution G A exon_variant MELA-AU 3 69097302 69097302 single base substitution G A missense_variant S185L 554C>T MELA-AU 3 69097302 69097302 single base substitution G A upstream_gene_variant MELA-AU 3 69097349 69097349 single base substitution T G exon_variant MELA-AU 3 69097349 69097349 single base substitution T G synonymous_variant S169S 507A>C MELA-AU 3 69097349 69097349 single base substitution T G upstream_gene_variant MELA-AU 3 69098356 69098356 single base substitution C T intron_variant MELA-AU 3 69098356 69098356 single base substitution C T upstream_gene_variant MELA-AU 3 69099229 69099229 single base substitution G A intron_variant MELA-AU 3 69101513 69101513 single base substitution G A upstream_gene_variant MELA-AU 3 69101627 69101627 single base substitution G A upstream_gene_variant MELA-AU 3 69102292 69102292 single base substitution G A upstream_gene_variant MELA-AU 3 69102357 69102357 single base substitution A T upstream_gene_variant MELA-AU 3 69102704 69102704 single base substitution G A upstream_gene_variant MELA-AU 3 69103152 69103152 single base substitution G A upstream_gene_variant MELA-AU 3 69103242 69103242 single base substitution G A upstream_gene_variant MELA-AU 3 69103529 69103529 single base substitution T A upstream_gene_variant MELA-AU 3 69104159 69104160 multiple base substitution (>=2bp and <=200bp) GT AG upstream_gene_variant MELA-AU 3 69104313 69104313 single base substitution G A upstream_gene_variant MELA-AU 3 69104602 69104602 single base substitution G A upstream_gene_variant MELA-AU 3 69105696 69105696 single base substitution T A upstream_gene_variant MELA-AU 3 69105974 69105974 single base substitution G A upstream_gene_variant MELA-AU 3 69106364 69106364 deletion of <=200bp A - upstream_gene_variant ORCA-IN 3 69102680 69102680 single base substitution T G upstream_gene_variant OV-AU 3 69065009 69065009 single base substitution G C downstream_gene_variant OV-AU 3 69071318 69071318 single base substitution A G 3_prime_UTR_variant OV-AU 3 69071318 69071318 single base substitution A G downstream_gene_variant OV-AU 3 69075439 69075439 single base substitution G A intron_variant OV-AU 3 69075439 69075439 single base substitution G A upstream_gene_variant OV-AU 3 69084712 69084712 single base substitution C T intron_variant OV-AU 3 69094597 69094597 single base substitution A C intron_variant OV-AU 3 69094597 69094597 single base substitution A C upstream_gene_variant OV-AU 3 69095974 69095974 single base substitution G C intron_variant OV-AU 3 69095974 69095974 single base substitution G C upstream_gene_variant OV-AU 3 69098357 69098357 single base substitution T G intron_variant OV-AU 3 69098357 69098357 single base substitution T G upstream_gene_variant OV-AU 3 69101426 69101426 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant OV-AU 3 69101643 69101643 single base substitution C T upstream_gene_variant OV-AU 3 69103171 69103171 single base substitution T C upstream_gene_variant PACA-AU 3 69072781 69072781 single base substitution C G downstream_gene_variant PACA-AU 3 69072781 69072781 single base substitution C G intron_variant PACA-AU 3 69072954 69072954 single base substitution T C downstream_gene_variant PACA-AU 3 69072954 69072954 single base substitution T C intron_variant PACA-AU 3 69076682 69076682 single base substitution T A intron_variant PACA-AU 3 69076682 69076682 single base substitution T A upstream_gene_variant PACA-AU 3 69078774 69078774 single base substitution G A intron_variant PACA-AU 3 69078774 69078774 single base substitution G A upstream_gene_variant PACA-AU 3 69078776 69078776 single base substitution G A intron_variant PACA-AU 3 69078776 69078776 single base substitution G A upstream_gene_variant PACA-AU 3 69079469 69079469 single base substitution C T intron_variant PACA-AU 3 69079469 69079469 single base substitution C T upstream_gene_variant PACA-AU 3 69091644 69091644 single base substitution C G downstream_gene_variant PACA-AU 3 69091644 69091644 single base substitution C G intron_variant PACA-AU 3 69094176 69094176 single base substitution G A intron_variant PACA-AU 3 69094176 69094176 single base substitution G A upstream_gene_variant PACA-AU 3 69099012 69099012 single base substitution G A intron_variant PACA-AU 3 69105310 69105310 single base substitution A G upstream_gene_variant PACA-CA 3 69069177 69069177 single base substitution C A 3_prime_UTR_variant PACA-CA 3 69069177 69069177 single base substitution C A downstream_gene_variant PACA-CA 3 69077601 69077601 single base substitution A C intron_variant PACA-CA 3 69077601 69077601 single base substitution A C upstream_gene_variant PACA-CA 3 69080126 69080126 single base substitution G C intron_variant PACA-CA 3 69080126 69080126 single base substitution G C upstream_gene_variant PACA-CA 3 69080691 69080691 single base substitution T A intron_variant PACA-CA 3 69083951 69083954 deletion of <=200bp ATCT - intron_variant PACA-CA 3 69085416 69085416 single base substitution G T intron_variant PACA-CA 3 69085650 69085650 single base substitution T A intron_variant PACA-CA 3 69086795 69086795 insertion of <=200bp - A intron_variant PACA-CA 3 69088599 69088599 single base substitution G A downstream_gene_variant PACA-CA 3 69088599 69088599 single base substitution G A intron_variant PACA-CA 3 69090088 69090088 single base substitution A T downstream_gene_variant PACA-CA 3 69090088 69090088 single base substitution A T intron_variant PACA-CA 3 69093220 69093220 single base substitution A G intron_variant PACA-CA 3 69093357 69093357 single base substitution T C intron_variant PACA-CA 3 69101173 69101173 single base substitution T G exon_variant PACA-CA 3 69101173 69101173 single base substitution T G missense_variant K22T 65A>C PACA-CA 3 69106458 69106458 single base substitution C T upstream_gene_variant PACA-CA 3 69106469 69106469 single base substitution A C upstream_gene_variant PAEN-AU 3 69104820 69104820 single base substitution A G upstream_gene_variant PAEN-IT 3 69076398 69076398 single base substitution C T intron_variant PAEN-IT 3 69076398 69076398 single base substitution C T upstream_gene_variant PBCA-DE 3 69093492 69093492 single base substitution G T intron_variant PRAD-UK 3 69069930 69069930 deletion of <=200bp G - 3_prime_UTR_variant PRAD-UK 3 69069930 69069930 deletion of <=200bp G - downstream_gene_variant PRAD-UK 3 69070518 69070518 single base substitution T C 3_prime_UTR_variant PRAD-UK 3 69070518 69070518 single base substitution T C downstream_gene_variant PRAD-UK 3 69072091 69072091 insertion of <=200bp - A 3_prime_UTR_variant PRAD-UK 3 69072091 69072091 insertion of <=200bp - A downstream_gene_variant PRAD-UK 3 69075495 69075495 single base substitution C T intron_variant PRAD-UK 3 69075495 69075495 single base substitution C T upstream_gene_variant PRAD-US 3 69075248 69075248 single base substitution C A exon_variant PRAD-US 3 69075248 69075248 single base substitution C A splice_region_variant PRAD-US 3 69075248 69075248 single base substitution C A stop_gained E920* 2758G>T PRAD-US 3 69075248 69075248 single base substitution C A stop_gained E923* 2767G>T PRAD-US 3 69097585 69097585 single base substitution C T exon_variant PRAD-US 3 69097585 69097585 single base substitution C T missense_variant D91N 271G>A PRAD-US 3 69097585 69097585 single base substitution C T upstream_gene_variant READ-US 3 69073286 69073286 single base substitution C A 3_prime_UTR_variant READ-US 3 69073286 69073286 single base substitution C A downstream_gene_variant READ-US 3 69073286 69073286 single base substitution C A stop_gained E1020* 3058G>T READ-US 3 69073286 69073286 single base substitution C A stop_gained E1023* 3067G>T READ-US 3 69077095 69077095 single base substitution C A 3_prime_UTR_variant READ-US 3 69077095 69077095 single base substitution C A stop_gained E905* 2713G>T READ-US 3 69077095 69077095 single base substitution C A stop_gained E908* 2722G>T READ-US 3 69077095 69077095 single base substitution C A upstream_gene_variant READ-US 3 69096730 69096730 single base substitution T C exon_variant READ-US 3 69096730 69096730 single base substitution T C missense_variant K376E 1126A>G READ-US 3 69096730 69096730 single base substitution T C upstream_gene_variant READ-US 3 69097306 69097306 single base substitution C A exon_variant READ-US 3 69097306 69097306 single base substitution C A stop_gained E184* 550G>T READ-US 3 69097306 69097306 single base substitution C A upstream_gene_variant RECA-EU 3 69066260 69066260 single base substitution T A downstream_gene_variant RECA-EU 3 69081780 69081780 single base substitution G T intron_variant RECA-EU 3 69084316 69084316 single base substitution A G intron_variant SKCA-BR 3 69065407 69065407 insertion of <=200bp - GGTTTGTGTGTGT downstream_gene_variant SKCA-BR 3 69065410 69065410 single base substitution G T downstream_gene_variant SKCA-BR 3 69065436 69065436 single base substitution G A downstream_gene_variant SKCA-BR 3 69073420 69073420 single base substitution T G downstream_gene_variant SKCA-BR 3 69073420 69073420 single base substitution T G intron_variant SKCA-BR 3 69077650 69077650 single base substitution A C intron_variant SKCA-BR 3 69077650 69077650 single base substitution A C upstream_gene_variant SKCA-BR 3 69078193 69078193 insertion of <=200bp - AT intron_variant SKCA-BR 3 69078193 69078193 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 3 69080722 69080722 single base substitution A G intron_variant SKCA-BR 3 69084273 69084273 single base substitution G A splice_region_variant SKCA-BR 3 69084599 69084599 single base substitution G A intron_variant SKCA-BR 3 69090649 69090649 single base substitution T A downstream_gene_variant SKCA-BR 3 69090649 69090649 single base substitution T A intron_variant SKCA-BR 3 69093133 69093133 single base substitution T C intron_variant SKCA-BR 3 69097477 69097477 single base substitution C T exon_variant SKCA-BR 3 69097477 69097477 single base substitution C T missense_variant E127K 379G>A SKCA-BR 3 69097477 69097477 single base substitution C T upstream_gene_variant SKCA-BR 3 69101513 69101513 single base substitution G A upstream_gene_variant SKCA-BR 3 69102714 69102714 single base substitution A T upstream_gene_variant SKCA-BR 3 69103441 69103441 single base substitution C G upstream_gene_variant SKCA-BR 3 69104624 69104624 single base substitution T G upstream_gene_variant SKCM-US 3 69079079 69079079 single base substitution C T exon_variant SKCM-US 3 69079079 69079079 single base substitution C T synonymous_variant Q827Q 2481G>A SKCM-US 3 69079079 69079079 single base substitution C T synonymous_variant Q830Q 2490G>A SKCM-US 3 69079079 69079079 single base substitution C T upstream_gene_variant SKCM-US 3 69079119 69079120 deletion of <=200bp TC - exon_variant SKCM-US 3 69079119 69079120 deletion of <=200bp TC - frameshift_variant E814 SKCM-US 3 69079119 69079120 deletion of <=200bp TC - frameshift_variant E817 SKCM-US 3 69079119 69079120 deletion of <=200bp TC - upstream_gene_variant SKCM-US 3 69088085 69088085 single base substitution G A downstream_gene_variant SKCM-US 3 69088085 69088085 single base substitution G A exon_variant SKCM-US 3 69088085 69088085 single base substitution G A stop_gained Q635* 1903C>T SKCM-US 3 69088085 69088085 single base substitution G A stop_gained Q638* 1912C>T SKCM-US 3 69092038 69092038 single base substitution A C downstream_gene_variant SKCM-US 3 69092038 69092038 single base substitution A C exon_variant SKCM-US 3 69092038 69092038 single base substitution A C missense_variant L535R 1604T>G SKCM-US 3 69092038 69092038 single base substitution A C missense_variant L538R 1613T>G SKCM-US 3 69092986 69092986 single base substitution G A exon_variant SKCM-US 3 69092986 69092986 single base substitution G A missense_variant S498F 1493C>T SKCM-US 3 69092986 69092986 single base substitution G A missense_variant S501F 1502C>T SKCM-US 3 69096510 69096510 single base substitution T A missense_variant K449M 1346A>T SKCM-US 3 69096510 69096510 single base substitution T A splice_region_variant SKCM-US 3 69096510 69096510 single base substitution T A upstream_gene_variant SKCM-US 3 69096520 69096520 single base substitution C T exon_variant SKCM-US 3 69096520 69096520 single base substitution C T missense_variant D446N 1336G>A SKCM-US 3 69096520 69096520 single base substitution C T upstream_gene_variant SKCM-US 3 69097377 69097377 single base substitution G A exon_variant SKCM-US 3 69097377 69097377 single base substitution G A missense_variant S160L 479C>T SKCM-US 3 69097377 69097377 single base substitution G A upstream_gene_variant SKCM-US 3 69097533 69097533 single base substitution G A exon_variant SKCM-US 3 69097533 69097533 single base substitution G A missense_variant T108I 323C>T SKCM-US 3 69097533 69097533 single base substitution G A upstream_gene_variant SKCM-US 3 69097638 69097638 single base substitution G A exon_variant SKCM-US 3 69097638 69097638 single base substitution G A missense_variant P73L 218C>T SKCM-US 3 69097638 69097638 single base substitution G A upstream_gene_variant SKCM-US 3 69097669 69097669 single base substitution C T exon_variant SKCM-US 3 69097669 69097669 single base substitution C T missense_variant G63R 187G>A SKCM-US 3 69097669 69097669 single base substitution C T upstream_gene_variant SKCM-US 3 69105771 69105771 single base substitution C T upstream_gene_variant STAD-US 3 69075185 69075185 single base substitution C T 3_prime_UTR_variant STAD-US 3 69075185 69075185 single base substitution C T exon_variant STAD-US 3 69075185 69075185 single base substitution C T missense_variant V941I 2821G>A STAD-US 3 69075185 69075185 single base substitution C T missense_variant V944I 2830G>A STAD-US 3 69077408 69077408 single base substitution A G 3_prime_UTR_variant STAD-US 3 69077408 69077408 single base substitution A G missense_variant V878A 2633T>C STAD-US 3 69077408 69077408 single base substitution A G missense_variant V881A 2642T>C STAD-US 3 69077408 69077408 single base substitution A G upstream_gene_variant STAD-US 3 69096977 69096977 single base substitution A C exon_variant STAD-US 3 69096977 69096977 single base substitution A C missense_variant F293L 879T>G STAD-US 3 69096977 69096977 single base substitution A C upstream_gene_variant STAD-US 3 69097100 69097100 single base substitution A G exon_variant STAD-US 3 69097100 69097100 single base substitution A G synonymous_variant G252G 756T>C STAD-US 3 69097100 69097100 single base substitution A G upstream_gene_variant STAD-US 3 69101186 69101186 single base substitution A G exon_variant STAD-US 3 69101186 69101186 single base substitution A G missense_variant S18P 52T>C STAD-US 3 69105035 69105035 single base substitution G A upstream_gene_variant THCA-SA 3 69070457 69070457 single base substitution G A 3_prime_UTR_variant THCA-SA 3 69070457 69070457 single base substitution G A downstream_gene_variant THCA-SA 3 69072361 69072364 deletion of <=200bp TTGA - 3_prime_UTR_variant THCA-SA 3 69072361 69072364 deletion of <=200bp TTGA - downstream_gene_variant THCA-SA 3 69072361 69072364 deletion of <=200bp TTGA - frameshift_variant TQ1082 THCA-SA 3 69072361 69072364 deletion of <=200bp TTGA - frameshift_variant TQ1085 THCA-SA 3 69096891 69096891 single base substitution G C exon_variant THCA-SA 3 69096891 69096891 single base substitution G C missense_variant A322G 965C>G THCA-SA 3 69096891 69096891 single base substitution G C upstream_gene_variant THCA-US 3 69088082 69088082 single base substitution C G downstream_gene_variant THCA-US 3 69088082 69088082 single base substitution C G exon_variant THCA-US 3 69088082 69088082 single base substitution C G missense_variant E636Q 1906G>C THCA-US 3 69088082 69088082 single base substitution C G missense_variant E639Q 1915G>C UCEC-US 3 69072387 69072387 single base substitution C A 3_prime_UTR_variant UCEC-US 3 69072387 69072387 single base substitution C A downstream_gene_variant UCEC-US 3 69072387 69072387 single base substitution C A missense_variant D1075Y 3223G>T UCEC-US 3 69072387 69072387 single base substitution C A missense_variant D1078Y 3232G>T UCEC-US 3 69077056 69077056 single base substitution C A 3_prime_UTR_variant UCEC-US 3 69077056 69077056 single base substitution C A stop_gained E918* 2752G>T UCEC-US 3 69077056 69077056 single base substitution C A stop_gained E921* 2761G>T UCEC-US 3 69077056 69077056 single base substitution C A upstream_gene_variant UCEC-US 3 69077068 69077068 single base substitution C A 3_prime_UTR_variant UCEC-US 3 69077068 69077068 single base substitution C A stop_gained E914* 2740G>T UCEC-US 3 69077068 69077068 single base substitution C A stop_gained E917* 2749G>T UCEC-US 3 69077068 69077068 single base substitution C A upstream_gene_variant UCEC-US 3 69077425 69077425 single base substitution G C 3_prime_UTR_variant UCEC-US 3 69077425 69077425 single base substitution G C missense_variant N872K 2616C>G UCEC-US 3 69077425 69077425 single base substitution G C missense_variant N875K 2625C>G UCEC-US 3 69077425 69077425 single base substitution G C upstream_gene_variant UCEC-US 3 69082718 69082718 single base substitution C A intron_variant UCEC-US 3 69082718 69082718 single base substitution C A missense_variant K794N 2382G>T UCEC-US 3 69082718 69082718 single base substitution C A missense_variant K797N 2391G>T UCEC-US 3 69087783 69087783 single base substitution C A exon_variant UCEC-US 3 69087783 69087783 single base substitution C A stop_gained E695* 2083G>T UCEC-US 3 69087783 69087783 single base substitution C A stop_gained E698* 2092G>T UCEC-US 3 69096604 69096604 single base substitution T C exon_variant UCEC-US 3 69096604 69096604 single base substitution T C missense_variant N418D 1252A>G UCEC-US 3 69096604 69096604 single base substitution T C upstream_gene_variant UCEC-US 3 69096784 69096784 insertion of <=200bp - AG exon_variant UCEC-US 3 69096784 69096784 insertion of <=200bp - AG frameshift_variant I358T? UCEC-US 3 69096784 69096784 insertion of <=200bp - AG upstream_gene_variant UCEC-US 3 69097037 69097037 single base substitution C T exon_variant UCEC-US 3 69097037 69097037 single base substitution C T synonymous_variant A273A 819G>A UCEC-US 3 69097037 69097037 single base substitution C T upstream_gene_variant UCEC-US 3 69097078 69097078 single base substitution C A exon_variant UCEC-US 3 69097078 69097078 single base substitution C A stop_gained E260* 778G>T UCEC-US 3 69097078 69097078 single base substitution C A upstream_gene_variant UCEC-US 3 69097301 69097301 single base substitution C T exon_variant UCEC-US 3 69097301 69097301 single base substitution C T synonymous_variant S185S 555G>A UCEC-US 3 69097301 69097301 single base substitution C T upstream_gene_variant UCEC-US 3 69097324 69097324 single base substitution C T exon_variant UCEC-US 3 69097324 69097324 single base substitution C T missense_variant E178K 532G>A UCEC-US 3 69097324 69097324 single base substitution C T upstream_gene_variant UCEC-US 3 69101175 69101175 single base substitution C T exon_variant UCEC-US 3 69101175 69101175 single base substitution C T synonymous_variant Q21Q 63G>A UCEC-US 3 69106448 69106448 single base substitution C A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T3236 COSM4734661 c.2716delA p.R906fs*11 Deletion - Frameshift 3:69027941-69027941 - ZZUFHECRKL-G067T COSM5438732 c.1426G>T p.E476* Substitution - Nonsense 3:69044517-69044517 - TCGA-BR-8589-01 COSM4119994 c.879T>G p.F293L Substitution - Missense 3:69047826-69047826 - HCT15 COSM2784426 c.1190G>A p.G397E Substitution - Missense 3:69047515-69047515 - ESO-632 COSM1268155 c.572C>G p.T191S Substitution - Missense 3:69048133-69048133 - TCGA-BS-A0UF-01 COSM1048260 c.2382G>T p.K794N Substitution - Missense 3:69033567-69033567 - MO_1128 COSM5566399 c.1667G>T p.R556L Substitution - Missense 3:69042824-69042824 - T2950 COSM4734668 c.1215_1216delTG p.C405fs*1 Deletion - Frameshift 3:69047489-69047490 - TCGA-06-5858-01 COSM1048264 c.819G>A p.A273A Substitution - coding silent 3:69047886-69047886 - ESO-752 COSM1268156 c.2253G>T p.Q751H Substitution - Missense 3:69033696-69033696 - T3225 COSM4734664 c.2229C>T p.I743I Substitution - coding silent 3:69035038-69035038 - TCGA-BS-A0UV-01 COSM1048258 c.2740G>T p.E914* Substitution - Nonsense 3:69027917-69027917 - SNUH_G10_S1 COSM4002813 c.1242C>G p.S414S Substitution - coding silent 3:69047463-69047463 - TCGA-CC-A3MC-01 COSM4919569 c.719A>G p.N240S Substitution - Missense 3:69047986-69047986 - TCGA-GV-A3QH-01 COSM1309455 c.559A>G p.M187V Substitution - Missense 3:69048146-69048146 - TCGA-39-5031-01 COSM731659 c.2774C>A p.S925Y Substitution - Missense 3:69026081-69026081 - TCGA-CC-A3MA-01 COSM4942754 c.2480A>G p.Q827R Substitution - Missense 3:69029929-69029929 - HN_00190 COSM129790 c.2489C>T p.S830F Substitution - Missense 3:69029920-69029920 - TCGA-G5-6641-01 COSM1567145 c.1126A>G p.K376E Substitution - Missense 3:69047579-69047579 - B89-10-Tumor COSM1753371 c.3097G>A p.E1033K Substitution - Missense 3:69024096-69024096 - TCGA-AX-A0J0-01 COSM1048261 c.2083G>T p.E695* Substitution - Nonsense 3:69038632-69038632 - TCGA-D9-A6EC-06 COSM4403329 c.1604T>G p.L535R Substitution - Missense 3:69042887-69042887 - TCGA-AD-6889-01 COSM1425191 c.2241G>A p.Q747Q Substitution - coding silent 3:69035026-69035026 - SC_9047 COSM5553510 c.1475A>G p.E492G Substitution - Missense 3:69043853-69043853 - PT41 COSM5924313 c.1889C>T p.S630F Substitution - Missense 3:69038948-69038948 - 66 COSM5742976 c.1901G>A p.R634H Substitution - Missense 3:69038936-69038936 - MedB-1 COSM5622014 c.1234G>A p.V412I Substitution - Missense 3:69047471-69047471 - TCGA-AP-A056-01 COSM1048267 c.532G>A p.E178K Substitution - Missense 3:69048173-69048173 - TCGA-BQ-5878-01 COSM3993309 c.27C>T p.L9L Substitution - coding silent 3:69052060-69052060 - TCGA-AA-A00N-01 COSM277736 c.1517G>T p.R506I Substitution - Missense 3:69043811-69043811 - pfg034T COSM4756952 c.931C>A p.Q311K Substitution - Missense 3:69047774-69047774 - CHEWS032 COSM2784414 c.2088T>C p.L696L Substitution - coding silent 3:69038627-69038627 - TCGA-AP-A059-01 COSM1048262 c.1252A>G p.N418D Substitution - Missense 3:69047453-69047453 - HCT-15 COSM1670339 c.644C>T p.T215M Substitution - Missense 3:69048061-69048061 - DN120A6 COSM5789816 c.592G>A p.E198K Substitution - Missense 3:69048113-69048113 - CSCC-10-T COSM4570889 c.341T>G p.V114G Substitution - Missense 3:69048364-69048364 - T578 COSM1048260 c.2382G>T p.K794N Substitution - Missense 3:69033567-69033567 - TCGA-Q1-A6DW-01 COSM4856021 c.29C>G p.S10C Substitution - Missense 3:69052058-69052058 - TCGA-AD-6895-01 COSM1425189 c.2980A>T p.K994* Substitution - Nonsense 3:69025592-69025592 - B86-Tumor COSM1753372 c.2630A>G p.Y877C Substitution - Missense 3:69028260-69028260 - PANTSM COSM5004230 c.2652G>C p.T884T Substitution - coding silent 3:69028238-69028238 - TCGA-FW-A5DY-06 COSM3597239 c.479C>T p.S160L Substitution - Missense 3:69048226-69048226 - HCC2998 COSM1670338 c.1690A>C p.K564Q Substitution - Missense 3:69039688-69039688 - TCGA-J4-A67O-01 COSM3783753 c.271G>A p.D91N Substitution - Missense 3:69048434-69048434 - TCGA-CA-6718-01 COSM1425193 c.1867G>T p.E623* Substitution - Nonsense 3:69038970-69038970 - ESO-2143 COSM1268153 c.2318G>A p.R773Q Substitution - Missense 3:69033631-69033631 - TCGA-AX-A0J1-01 COSM1048266 c.555G>A p.S185S Substitution - coding silent 3:69048150-69048150 - Case2d COSM1717129 c.1533A>T p.E511D Substitution - Missense 3:69043795-69043795 - 2492730 COSM5728760 c.546T>C p.N182N Substitution - coding silent 3:69048159-69048159 - P03-871 COSM247909 c.3241A>G p.K1081E Substitution - Missense 3:69023218-69023218 - EGC8 COSM5059938 c.2800C>T p.R934C Substitution - Missense 3:69026055-69026055 - PD11345a COSM5789816 c.592G>A p.E198K Substitution - Missense 3:69048113-69048113 - PCSI_0083_Pa_P_526 COSM3781858 c.65A>C p.K22T Substitution - Missense 3:69052022-69052022 - TCGA-EL-A3CR-01 COSM3373292 c.1906G>C p.E636Q Substitution - Missense 3:69038931-69038931 - SC_9012 COSM5562113 c.905C>T p.P302L Substitution - Missense 3:69047800-69047800 - 391 COSM4427955 c.1799T>C p.L600P Substitution - Missense 3:69039579-69039579 - TCGA-EP-A3JL-01 COSM4913940 c.2180G>T p.R727L Substitution - Missense 3:69035087-69035087 - TCGA-AX-A05Z-01 COSM1048264 c.819G>A p.A273A Substitution - coding silent 3:69047886-69047886 - 587376 COSM1048258 c.2740G>T p.E914* Substitution - Nonsense 3:69027917-69027917 - TCGA-EE-A29D-06 COSM3597235 c.2481G>A p.Q827Q Substitution - coding silent 3:69029928-69029928 - HCT15 COSM1670339 c.644C>T p.T215M Substitution - Missense 3:69048061-69048061 - pfg016T COSM1642343 c.383_385delAAG p.E128delE Deletion - In frame 3:69048320-69048322 - TCGA-76-6664-01 COSM3408873 c.371G>A p.R124Q Substitution - Missense 3:69048334-69048334 - LUAD-RT-S01711 COSM380177 c.2193G>T p.A731A Substitution - coding silent 3:69035074-69035074 - CR108 COSM4994763 c.3163A>C p.I1055L Substitution - Missense 3:69023296-69023296 - STC297 COSM5059939 c.1567G>A p.A523T Substitution - Missense 3:69043761-69043761 - 587376 COSM1048261 c.2083G>T p.E695* Substitution - Nonsense 3:69038632-69038632 - TCGA-39-5016-01 COSM731657 c.634A>T p.N212Y Substitution - Missense 3:69048071-69048071 - TCGA-CM-6171-01 COSM1425192 c.1921C>T p.R641C Substitution - Missense 3:69038916-69038916 - TCGA-GF-A6C9-06 COSM4900386 c.218C>T p.P73L Substitution - Missense 3:69048487-69048487 - T155 COSM1177259 c.382G>T p.E128* Substitution - Nonsense 3:69048323-69048323 - TCGA-18-4083-01 COSM584596 c.36C>T p.F12F Substitution - coding silent 3:69052051-69052051 - 049T COSM1729877 c.3148C>A p.Q1050K Substitution - Missense 3:69023311-69023311 - HCC066T COSM5821586 c.104C>G p.P35R Substitution - Missense 3:69051983-69051983 - B65-Tumor COSM1753373 c.2521G>C p.E841Q Substitution - Missense 3:69029888-69029888 - TCGA-A4-A6HP-01 COSM3993308 c.3150A>G p.Q1050Q Substitution - coding silent 3:69023309-69023309 - T3 COSM5344533 c.425C>T p.S142L Substitution - Missense 3:69048280-69048280 - T3174 COSM4734667 c.1565_1566insGA p.D522fs*11 Insertion - Frameshift 3:69043762-69043763 - T2269 COSM4734666 c.1691A>T p.K564I Substitution - Missense 3:69039687-69039687 - TCGA-D8-A1JA-01 COSM3824590 c.1117G>A p.A373T Substitution - Missense 3:69047588-69047588 - TCGA-AX-A0J0-01 COSM1048265 c.778G>T p.E260* Substitution - Nonsense 3:69047927-69047927 - 2186 COSM5017026 c.256C>T p.R86W Substitution - Missense 3:69048449-69048449 - CSCC-49-T COSM4559065 c.78G>A p.R26R Substitution - coding silent 3:69052009-69052009 - T207 COSM4734670 c.467_469delCTT p.S156delS Deletion - In frame 3:69048236-69048238 - TCGA-DK-A1AC-01 COSM1309454 c.2869C>T p.H957Y Substitution - Missense 3:69025703-69025703 - TCGA-CA-6717-01 COSM1425196 c.1081A>C p.N361H Substitution - Missense 3:69047624-69047624 - 587376 COSM1229769 c.2905A>C p.N969H Substitution - Missense 3:69025667-69025667 - TCGA-CA-6718-01 COSM1425195 c.1731G>T p.K577N Substitution - Missense 3:69039647-69039647 - TCGA-GF-A6C9-06 COSM4903619 c.187G>A p.G63R Substitution - Missense 3:69048518-69048518 - BCM617T COSM4955974 c.639G>T p.T213T Substitution - coding silent 3:69048066-69048066 - PTC_435 COSM5957237 c.965C>G p.A322G Substitution - Missense 3:69047740-69047740 - Pat_44_B COSM5865264 c.574G>A p.V192I Substitution - Missense 3:69048131-69048131 - TCGA-BS-A0UF-01 COSM1048256 c.3223G>T p.D1075Y Substitution - Missense 3:69023236-69023236 - RK288_C01 COSM4780481 c.1578G>A p.K526K Substitution - coding silent 3:69043750-69043750 - 587376 COSM1229770 c.1193G>A p.R398Q Substitution - Missense 3:69047512-69047512 - TCGA-AX-A05Z-01 COSM1048268 c.63G>A p.Q21Q Substitution - coding silent 3:69052024-69052024 - PTC-28C COSM4158308 c.1711C>A p.H571N Substitution - Missense 3:69039667-69039667 - LIM1899 COSM4613104 c.3037_3038insA p.T1013fs*7 Insertion - Frameshift 3:69024155-69024156 - 587234 COSM1229768 c.209C>A p.P70H Substitution - Missense 3:69048496-69048496 - TCGA-22-1016-01 COSM731660 c.3204A>G p.E1068E Substitution - coding silent 3:69023255-69023255 - TCGA-BR-A4CS-01 COSM4119996 c.52T>C p.S18P Substitution - Missense 3:69052035-69052035 - TCGA-HU-A4H4-01 COSM4119993 c.2633T>C p.V878A Substitution - Missense 3:69028257-69028257 - TCGA-AM-5821-01 COSM3760218 c.2392G>C p.D798H Substitution - Missense 3:69033557-69033557 - TCGA-EI-6917-01 COSM3427857 c.2713G>T p.E905* Substitution - Nonsense 3:69027944-69027944 - T1240 COSM1425192 c.1921C>T p.R641C Substitution - Missense 3:69038916-69038916 - ODG3 COSM5444654 c.2718G>A p.R906R Substitution - coding silent 3:69027939-69027939 - TCGA-D9-A6EC-06 COSM4401882 c.1346A>T p.K449M Substitution - Missense 3:69047359-69047359 - TCGA-AC-A23H-01 COSM3824591 c.356C>T p.P119L Substitution - Missense 3:69048349-69048349 - cSCCP6 COSM136358 c.3031G>A p.E1011K Substitution - Missense 3:69024162-69024162 - TCGA-AP-A056-01 COSM1048263 c.1071_1072insCT p.I358fs*3 Insertion - Frameshift 3:69047633-69047634 - YUROC COSM5399982 c.1815G>A p.Q605Q Substitution - coding silent 3:69039563-69039563 - TCGA-DR-A0ZM-01 COSM460739 c.3079C>G p.Q1027E Substitution - Missense 3:69024114-69024114 - TCGA-FU-A3HZ-01 COSM4840686 c.1447A>C p.K483Q Substitution - Missense 3:69044496-69044496 - 25 COSM4166997 c.2257G>A p.A753T Substitution - Missense 3:69033692-69033692 - T3024 COSM4734662 c.2346G>C p.L782L Substitution - coding silent 3:69033603-69033603 - SS6003149 COSM4091169 c.248A>G p.K83R Substitution - Missense 3:69048457-69048457 - TCGA-EK-A3GK-01 COSM4853646 c.2857C>G p.Q953E Substitution - Missense 3:69025998-69025998 - RK120_C01 COSM3702474 c.973A>G p.R325G Substitution - Missense 3:69047732-69047732 - B25 COSM1753374 c.318C>G p.V106V Substitution - coding silent 3:69048387-69048387 - TCGA-CA-6718-01 COSM1425194 c.1814A>G p.Q605R Substitution - Missense 3:69039564-69039564 - TCGA-AK-3447-01 COSM1495617 c.1994+2T>A p.? Unknown 3:69038841-69038841 - TCGA-F5-6814-01 COSM3427858 c.550G>T p.E184* Substitution - Nonsense 3:69048155-69048155 - HCC2998 COSM2784433 c.645G>A p.T215T Substitution - coding silent 3:69048060-69048060 - I2L-P19Ta-Tumor-Organoid COSM5354974 c.1650_1651delGA p.K551fs*2 Deletion - Frameshift 3:69042840-69042841 - PTC_285 COSM5959114 c.3246_3249delTCAA p.Q1083fs*1 Deletion - Frameshift 3:69023210-69023213 - TCGA-EE-A29W-06 COSM3597240 c.323C>T p.T108I Substitution - Missense 3:69048382-69048382 - TCGA-EB-A3XC-01 COSM3597238 c.1336G>A p.D446N Substitution - Missense 3:69047369-69047369 - TCGA-EI-6917-01 COSM3427856 c.3058G>T p.E1020* Substitution - Nonsense 3:69024135-69024135 - TCGA-AD-6895-01 COSM1309454 c.2869C>T p.H957Y Substitution - Missense 3:69025703-69025703 - PCSI_0083_Pa_X COSM3781858 c.65A>C p.K22T Substitution - Missense 3:69052022-69052022 - DLD1 COSM2784426 c.1190G>A p.G397E Substitution - Missense 3:69047515-69047515 - I2L-P19Ta-Tumor-Biopsy COSM5354974 c.1650_1651delGA p.K551fs*2 Deletion - Frameshift 3:69042840-69042841 - 522 COSM5612182 c.2957T>C p.I986T Substitution - Missense 3:69025615-69025615 - 585272 COSM326702 c.3095A>T p.E1032V Substitution - Missense 3:69024098-69024098 - LIM2405 COSM2784438 c.306G>A p.S102S Substitution - coding silent 3:69048399-69048399 - TCGA-24-1563-01 COSM1328078 c.2245-1_2245GA>TC p.? Unknown 3:69033704-69033705 - TCGA-B5-A11E-01 COSM1048264 c.819G>A p.A273A Substitution - coding silent 3:69047886-69047886 - TCGA-D1-A16Y-01 COSM1048259 c.2616C>G p.N872K Substitution - Missense 3:69028274-69028274 - TCGA-06-2559-01 COSM3408872 c.2765A>G p.K922R Substitution - Missense 3:69026090-69026090 - TCGA-60-2709-01 COSM731658 c.755G>T p.G252V Substitution - Missense 3:69047950-69047950 - BCM617T COSM4955974 c.639G>T p.T213T Substitution - coding silent 3:69048066-69048066 - TCGA-AX-A05Z-01 COSM1048260 c.2382G>T p.K794N Substitution - Missense 3:69033567-69033567 - V-PH-17T COSM4770430 c.598G>C p.V200L Substitution - Missense 3:69048107-69048107 - B86 COSM1753372 c.2630A>G p.Y877C Substitution - Missense 3:69028260-69028260 - B89-10 COSM1753371 c.3097G>A p.E1033K Substitution - Missense 3:69024096-69024096 - 23 COSM5748436 c.2329A>C p.N777H Substitution - Missense 3:69033620-69033620 - TCGA-BR-A4QL-01 COSM4119995 c.756T>C p.G252G Substitution - coding silent 3:69047949-69047949 - TCGA-D3-A1QB-06 COSM3597236 c.1903C>T p.Q635* Substitution - Nonsense 3:69038934-69038934 - TCGA-AY-6197-01 COSM1425198 c.186G>A p.W62* Substitution - Nonsense 3:69048519-69048519 - TCGA-A8-A0A6-01 COSM3824588 c.2153T>G p.V718G Substitution - Missense 3:69035114-69035114 - LUAD-F00121 COSM365803 c.2083G>C p.E695Q Substitution - Missense 3:69038632-69038632 - B65 COSM1753373 c.2521G>C p.E841Q Substitution - Missense 3:69029888-69029888 - T3298 COSM4734669 c.687T>C p.P229P Substitution - coding silent 3:69048018-69048018 - TCGA-AZ-4315-01 COSM1425190 c.2696G>T p.R899I Substitution - Missense 3:69027961-69027961 - TCGA-CM-6674-01 COSM1425188 c.3155A>G p.Y1052C Substitution - Missense 3:69023304-69023304 - ESO-582 COSM1268154 c.443C>G p.T148S Substitution - Missense 3:69048262-69048262 - HCA7 COSM4630901 c.1417G>A p.A473T Substitution - Missense 3:69044526-69044526 - TCGA-CZ-5985-01 COSM480557 c.3084T>G p.N1028K Substitution - Missense 3:69024109-69024109 - B25-Tumor COSM1753374 c.318C>G p.V106V Substitution - coding silent 3:69048387-69048387 - T2284 COSM4734665 c.2218C>T p.R740C Substitution - Missense 3:69035049-69035049 - HCC2998 COSM1670338 c.1690A>C p.K564Q Substitution - Missense 3:69039688-69039688 - SC_9009 COSM5552367 c.172G>T p.D58Y Substitution - Missense 3:69048533-69048533 - TCGA-CC-A7IH-01 COSM4924372 c.802A>G p.I268V Substitution - Missense 3:69047903-69047903 - TCGA-EE-A3AC-06 COSM3597237 c.1493C>T p.S498F Substitution - Missense 3:69043835-69043835 - 587376 COSM1229771 c.974G>T p.R325I Substitution - Missense 3:69047731-69047731 - Pat_14_A COSM5865265 c.365C>T p.S122L Substitution - Missense 3:69048340-69048340 - T2766 COSM4734663 c.2309C>T p.P770L Substitution - Missense 3:69033640-69033640 - ESCC_BICR_066T COSM5444654 c.2718G>A p.R906R Substitution - coding silent 3:69027939-69027939 - TCGA-EJ-7788-01 COSM3674030 c.2758G>T p.E920* Substitution - Nonsense 3:69026097-69026097 - PA285 COSM1163352 c.582G>A p.L194L Substitution - coding silent 3:69048123-69048123 - TCGA-G4-6588-01 COSM1425197 c.706G>T p.D236Y Substitution - Missense 3:69047999-69047999 - TCGA-AA-A010-01 COSM285824 c.1564G>A p.D522N Substitution - Missense 3:69043764-69043764 - TCGA-AR-A252-01 COSM1485461 c.3270A>G p.Q1090Q Substitution - coding silent 3:69023189-69023189 - TCGA-AN-A046-01 COSM3824589 c.1961G>A p.R654Q Substitution - Missense 3:69038876-69038876 - TCGA-D7-6527-01 COSM4119992 c.2821G>A p.V941I Substitution - Missense 3:69026034-69026034 - TCGA-BS-A0UF-01 COSM1048257 c.2752G>T p.E918* Substitution - Nonsense 3:69027905-69027905 - TCGA-AA-A00N-01 COSM277735 c.2023G>A p.A675T Substitution - Missense 3:69038692-69038692 - DLD1 COSM1670339 c.644C>T p.T215M Substitution - Missense 3:69048061-69048061 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.267632 3p21-p12 601126

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.N1028K c.3084T>G 3 69073260 RCCC A G Missense p.L1073P c.3218T>C 3 69072392 CM C A Missense p.A685S c.2053G>T 3 69087813 LUAD C A Missense p.G252V c.755G>T 3 69097101 LUSC C A Missense p.Q751H c.2253G>T 3 69082847 ESCA C A Missense p.R844I c.2531G>T 3 69079029 LUAD C A Nonsense p.E920* c.2758G>T 3 69075248 PRAD C G Missense p.E636Q c.1906G>C 3 69088082 THCA C T Missense p.D1029N c.3085G>A 3 69073259 HNSC C T Missense p.D1029N c.3085G>A 3 69073259 LUAD C T Missense p.D91N c.271G>A 3 69097585 PRAD C T Missense p.R124Q c.371G>A 3 69097485 GBM C T Missense p.R773Q c.2318G>A 3 69082782 ESCA C T Missense p.V941I c.2821G>A 3 69075185 STAD C T Synonymous p.E443E c.1329G>A 3 69096527 CM CTT - InFrameDeletion p.E128delE c.383_385delAAG 3 69097471 STAD G A Missense p.S498F c.1493C>T 3 69092986 CM G A Missense p.S830F c.2489C>T 3 69079071 HNSC G A Missense p.T108I c.323C>T 3 69097533 CM G A Nonsense p.Q635* c.1903C>T 3 69088085 CM G A Nonsense p.Q657* c.1969C>T 3 69088019 HNSC G A Synonymous p.F12F c.36C>T 3 69101202 LUAD G A Synonymous p.F12F c.36C>T 3 69101202 LUSC G A Synonymous p.L296L c.888C>T 3 69096968 LUAD G C Missense p.N872K c.2616C>G 3 69077425 UCEC G C Missense p.T148S c.443C>G 3 69097413 ESCA G C Missense p.T191S c.572C>G 3 69097284 ESCA G T Missense p.S925Y c.2774C>A 3 69075232 LUSC T A Missense p.D236V c.707A>T 3 69097149 STAD T A Missense p.E1032V c.3095A>T 3 69073249 SCLC T A Missense p.K693I c.2078A>T 3 69087788 MM T A Missense p.N212Y c.634A>T 3 69097222 LUSC TC - Frameshift p.E814Tfs*10 c.2440_2441delGA 3 69079119 CM TC GA SpliceAcceptorBlockSubstitution . c.2245-1_2245delinsTC 3 69082855 OV T C Missense p.K922R c.2765A>G 3 69075241 GBM T C Missense p.T191A c.571A>G 3 69097285 LUAD T C Missense p.T222A c.664A>G 3 69097192 LUAD T C Missense p.Y304C c.911A>G 3 69096945 HNSC T C Synonymous p.E1068E c.3204A>G 3 69072406 LUSC T C Synonymous p.Q1090Q c.3270A>G 3 69072340 BRCA