Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 23 16871808 16871808 + Missense_Mutation SNP A A G TCGA-OR-A5LP-01A-11D-A29I-10 TCGA-OR-A5LP-10A-01D-A29L-10 g.chrX:16871808A>G c.755T>C c.(754-756)aTg>aCg p.M252T BLCA 23 16864007 16864007 + Nonsense_Mutation SNP C C A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chrX:16864007C>A c.1153G>T c.(1153-1155)Gag>Tag p.E385* BLCA 23 16864054 16864054 + Missense_Mutation SNP T T A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chrX:16864054T>A c.1106A>T c.(1105-1107)cAt>cTt p.H369L BLCA 23 16876880 16876880 + Missense_Mutation SNP G G T TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chrX:16876880G>T c.400C>A c.(400-402)Cag>Aag p.Q134K BLCA 23 16876951 16876951 + Missense_Mutation SNP A A G TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chrX:16876951A>G c.329T>C c.(328-330)gTa>gCa p.V110A BLCA 23 16881165 16881165 + Missense_Mutation SNP C C T TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chrX:16881165C>T c.220G>A c.(220-222)Gag>Aag p.E74K BLCA 23 16887315 16887315 + Silent SNP G G C TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chrX:16887315G>C c.45C>G c.(43-45)gtC>gtG p.V15V BLCA 23 16887338 16887338 + Missense_Mutation SNP C C G TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chrX:16887338C>G c.22G>C c.(22-24)Gaa>Caa p.E8Q BRCA 23 16863181 16863181 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:16863181C>T c.1255G>A c.(1255-1257)Gaa>Aaa p.E419K BRCA 23 16863950 16863950 + Splice_Site SNP C C A TCGA-AC-A23C-01A-12D-A167-09 TCGA-AC-A23C-10A-01D-A167-09 g.chrX:16863950C>A c.e11+1 BRCA 23 16871848 16871848 + Missense_Mutation SNP C C G TCGA-AO-A1KS-01A-11D-A13L-09 TCGA-AO-A1KS-10A-01W-A14R-09 g.chrX:16871848C>G c.715G>C c.(715-717)Gag>Cag p.E239Q BRCA 23 16887272 16887272 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:16887272G>T c.88C>A c.(88-90)Cta>Ata p.L30I CESC 23 16870688 16870688 + Missense_Mutation SNP C C T TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chrX:16870688C>T c.949G>A c.(949-951)Gat>Aat p.D317N COAD 23 16863189 16863189 + Missense_Mutation SNP G G A TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chrX:16863189G>A c.1247C>T c.(1246-1248)aCg>aTg p.T416M COAD 23 16864001 16864001 + Frame_Shift_Del DEL A A - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chrX:16864001delA c.1159delT c.(1159-1161)tggfs p.W387fs COAD 23 16870190 16870190 + Missense_Mutation SNP C C T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chrX:16870190C>T c.1019G>A c.(1018-1020)cGc>cAc p.R340H COAD 23 16870194 16870194 + Missense_Mutation SNP G G T TCGA-A6-2671-01A-01D-1408-10 TCGA-A6-2671-10A-01D-1408-10 g.chrX:16870194G>T c.1015C>A c.(1015-1017)Cgc>Agc p.R339S COAD 23 16870679 16870679 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:16870679A>C c.958T>G c.(958-960)Ttc>Gtc p.F320V COAD 23 16870700 16870700 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:16870700C>T c.937G>A c.(937-939)Gaa>Aaa p.E313K COAD 23 16870701 16870701 + Silent SNP G G A TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chrX:16870701G>A c.936C>T c.(934-936)ttC>ttT p.F312F COAD 23 16870703 16870703 + Missense_Mutation SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chrX:16870703A>G c.934T>C c.(934-936)Ttc>Ctc p.F312L COAD 23 16870703 16870703 + Missense_Mutation SNP A A G TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chrX:16870703A>G c.934T>C c.(934-936)Ttc>Ctc p.F312L COAD 23 16870930 16870930 + Missense_Mutation SNP T T C TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chrX:16870930T>C c.827A>G c.(826-828)aAc>aGc p.N276S COAD 23 16870937 16870937 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:16870937C>T c.820G>A c.(820-822)Gaa>Aaa p.E274K COAD 23 16870937 16870937 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:16870937C>T c.820G>A c.(820-822)Gaa>Aaa p.E274K COAD 23 16870948 16870948 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:16870948G>A c.809C>T c.(808-810)gCg>gTg p.A270V COAD 23 16876898 16876898 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:16876898G>A c.382C>T c.(382-384)Cgt>Tgt p.R128C COAD 23 16876898 16876898 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:16876898G>A c.382C>T c.(382-384)Cgt>Tgt p.R128C COAD 23 16887283 16887285 + In_Frame_Del DEL TTC TTC - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chrX:16887283_16887285delTTC c.75_77delGAA c.(73-78)aagaat>aat p.K25del COAD 23 16887317 16887317 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chrX:16887317C>T c.43G>A c.(43-45)Gtc>Atc p.V15I COADREAD 23 16863189 16863189 + Missense_Mutation SNP G G A TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chrX:16863189G>A c.1247C>T c.(1246-1248)aCg>aTg p.T416M COADREAD 23 16864001 16864001 + Frame_Shift_Del DEL A A - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chrX:16864001delA c.1159delT c.(1159-1161)tggfs p.W387fs COADREAD 23 16870190 16870190 + Missense_Mutation SNP C C T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chrX:16870190C>T c.1019G>A c.(1018-1020)cGc>cAc p.R340H COADREAD 23 16870190 16870190 + Missense_Mutation SNP C C T TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chrX:16870190C>T c.1019G>A c.(1018-1020)cGc>cAc p.R340H COADREAD 23 16870194 16870194 + Missense_Mutation SNP G G T TCGA-A6-2671-01A-01D-1408-10 TCGA-A6-2671-10A-01D-1408-10 g.chrX:16870194G>T c.1015C>A c.(1015-1017)Cgc>Agc p.R339S COADREAD 23 16870679 16870679 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:16870679A>C c.958T>G c.(958-960)Ttc>Gtc p.F320V COADREAD 23 16870700 16870700 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:16870700C>T c.937G>A c.(937-939)Gaa>Aaa p.E313K COADREAD 23 16870700 16870700 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:16870700C>T c.937G>A c.(937-939)Gaa>Aaa p.E313K COADREAD 23 16870701 16870701 + Silent SNP G G A TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chrX:16870701G>A c.936C>T c.(934-936)ttC>ttT p.F312F COADREAD 23 16870703 16870703 + Missense_Mutation SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chrX:16870703A>G c.934T>C c.(934-936)Ttc>Ctc p.F312L COADREAD 23 16870703 16870703 + Missense_Mutation SNP A A G TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chrX:16870703A>G c.934T>C c.(934-936)Ttc>Ctc p.F312L COADREAD 23 16870930 16870930 + Missense_Mutation SNP T T C TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chrX:16870930T>C c.827A>G c.(826-828)aAc>aGc p.N276S COADREAD 23 16870937 16870937 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:16870937C>T c.820G>A c.(820-822)Gaa>Aaa p.E274K COADREAD 23 16870937 16870937 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:16870937C>T c.820G>A c.(820-822)Gaa>Aaa p.E274K COADREAD 23 16870948 16870948 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:16870948G>A c.809C>T c.(808-810)gCg>gTg p.A270V COADREAD 23 16876898 16876898 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:16876898G>A c.382C>T c.(382-384)Cgt>Tgt p.R128C COADREAD 23 16876898 16876898 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:16876898G>A c.382C>T c.(382-384)Cgt>Tgt p.R128C COADREAD 23 16887283 16887285 + In_Frame_Del DEL TTC TTC - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chrX:16887283_16887285delTTC c.75_77delGAA c.(73-78)aagaat>aat p.K25del COADREAD 23 16887317 16887317 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chrX:16887317C>T c.43G>A c.(43-45)Gtc>Atc p.V15I DLBC 23 16881137 16881137 + Missense_Mutation SNP A A C TCGA-GS-A9TT-01A-11D-A382-10 TCGA-GS-A9TT-10A-01D-A385-10 g.chrX:16881137A>C c.248T>G c.(247-249)gTa>gGa p.V83G ESCA 23 16864049 16864050 + Frame_Shift_Del DEL CT CT - TCGA-IG-A51D-01A-11D-A27G-09 TCGA-IG-A51D-10A-01D-A27G-09 g.chrX:16864049_16864050delCT c.1110_1111delAG c.(1108-1113)ggaggafs p.GG370fs ESCA 23 16887221 16887221 + Nonsense_Mutation SNP G G A TCGA-Z6-A8JE-01A-11D-A37C-09 TCGA-Z6-A8JE-10A-01D-A37F-09 g.chrX:16887221G>A c.139C>T c.(139-141)Cag>Tag p.Q47* GBMLGG 23 16863952 16863952 + Splice_Site SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:16863952A>G c.1208T>C c.(1207-1209)aTg>aCg p.M403T GBMLGG 23 16870701 16870701 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:16870701G>A c.936C>T c.(934-936)ttC>ttT p.F312F GBMLGG 23 16887194 16887197 + Splice_Site DEL CTTA CTTA - TCGA-HT-A5R9-01A-11D-A289-08 TCGA-HT-A5R9-10A-01D-A289-08 g.chrX:16887194_16887197delCTTA c.e2+1 HNSC 23 16863980 16863980 + Missense_Mutation SNP C C G TCGA-CV-6955-01A-11D-2012-08 TCGA-CV-6955-10A-01D-2013-08 g.chrX:16863980C>G c.1180G>C c.(1180-1182)Gag>Cag p.E394Q HNSC 23 16870184 16870184 + Missense_Mutation SNP T T G TCGA-CR-7376-01A-11D-2129-08 TCGA-CR-7376-10A-01D-2129-08 g.chrX:16870184T>G c.1025A>C c.(1024-1026)aAt>aCt p.N342T HNSC 23 16871871 16871871 + Missense_Mutation SNP T T A TCGA-CQ-A4C9-01A-11D-A25D-08 TCGA-CQ-A4C9-10A-01D-A25E-08 g.chrX:16871871T>A c.692A>T c.(691-693)gAt>gTt p.D231V HNSC 23 16887232 16887232 + Missense_Mutation SNP C C A TCGA-CV-7423-01A-11D-2078-08 TCGA-CV-7423-10A-01D-2078-08 g.chrX:16887232C>A c.128G>T c.(127-129)aGt>aTt p.S43I HNSC 23 16887237 16887237 + Missense_Mutation SNP C C G TCGA-CV-7423-01A-11D-2078-08 TCGA-CV-7423-10A-01D-2078-08 g.chrX:16887237C>G c.123G>C c.(121-123)tgG>tgC p.W41C HNSC 23 16887242 16887242 + Nonsense_Mutation SNP G G A TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chrX:16887242G>A c.118C>T c.(118-120)Cag>Tag p.Q40* HNSC 23 16887263 16887263 + Missense_Mutation SNP G G C TCGA-BA-A6DJ-01A-11D-A30E-08 TCGA-BA-A6DJ-10A-01D-A30H-08 g.chrX:16887263G>C c.97C>G c.(97-99)Ctg>Gtg p.L33V KIPAN 23 16864059 16864059 + Silent SNP A A G TCGA-G7-6793-01A-11D-1961-08 TCGA-G7-6793-10A-01D-1962-08 g.chrX:16864059A>G c.1101T>C c.(1099-1101)ttT>ttC p.F367F KIRP 23 16864059 16864059 + Silent SNP A A G TCGA-G7-6793-01A-11D-1961-08 TCGA-G7-6793-10A-01D-1962-08 g.chrX:16864059A>G c.1101T>C c.(1099-1101)ttT>ttC p.F367F LGG 23 16863952 16863952 + Splice_Site SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:16863952A>G c.1208T>C c.(1207-1209)aTg>aCg p.M403T LGG 23 16870701 16870701 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:16870701G>A c.936C>T c.(934-936)ttC>ttT p.F312F LGG 23 16887194 16887197 + Splice_Site DEL CTTA CTTA - TCGA-HT-A5R9-01A-11D-A289-08 TCGA-HT-A5R9-10A-01D-A289-08 g.chrX:16887194_16887197delCTTA c.e2+1 LIHC 23 16876872 16876872 + Silent SNP A A G TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chrX:16876872A>G c.408T>C c.(406-408)ccT>ccC p.P136P LIHC 23 16876930 16876930 + Missense_Mutation SNP T T C TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chrX:16876930T>C c.350A>G c.(349-351)gAa>gGa p.E117G LUAD 23 16867404 16867404 + Nonsense_Mutation SNP G G C TCGA-97-A4M5-01A-11D-A24P-08 TCGA-97-A4M5-10A-01D-A24P-08 g.chrX:16867404G>C c.1061C>G c.(1060-1062)tCa>tGa p.S354* LUAD 23 16870189 16870189 + Silent SNP G G T TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chrX:16870189G>T c.1020C>A c.(1018-1020)cgC>cgA p.R340R LUAD 23 16870709 16870709 + Frame_Shift_Del DEL G G - TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chrX:16870709delG c.928delC c.(928-930)catfs p.H310fs LUAD 23 16875781 16875781 + Missense_Mutation SNP T T C TCGA-50-8459-01A-11D-2323-08 TCGA-50-8459-10A-01D-2323-08 g.chrX:16875781T>C c.533A>G c.(532-534)gAa>gGa p.E178G LUAD 23 16888165 16888165 + Frame_Shift_Del DEL T T - TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chrX:16888165delT c.12delA c.(10-12)aaafs p.K4fs LUSC 23 16881153 16881153 + Silent SNP G G A TCGA-33-4547-01A-01D-1267-08 TCGA-33-4547-11A-01D-1267-08 g.chrX:16881153G>A c.232C>T c.(232-234)Ctg>Ttg p.L78L OV 23 16870701 16870701 + Silent SNP G G A TCGA-10-0931-01A-01W-0420-08 TCGA-10-0931-11A-01W-0420-08 g.chrX:16870701G>A c.936C>T c.(934-936)ttC>ttT p.F312F READ 23 16870190 16870190 + Missense_Mutation SNP C C T TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chrX:16870190C>T c.1019G>A c.(1018-1020)cGc>cAc p.R340H READ 23 16870700 16870700 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:16870700C>T c.937G>A c.(937-939)Gaa>Aaa p.E313K SARC 23 16875794 16875794 + Missense_Mutation SNP C C G TCGA-FX-A3RE-01A-11D-A228-09 TCGA-FX-A3RE-10A-01D-A22A-09 g.chrX:16875794C>G c.520G>C c.(520-522)Ggt>Cgt p.G174R SARC 23 16875809 16875809 + Missense_Mutation SNP C C A TCGA-3B-A9HX-01A-11D-A38Z-09 TCGA-3B-A9HX-10A-01D-A38Z-09 g.chrX:16875809C>A c.505G>T c.(505-507)Gat>Tat p.D169Y SKCM 23 16870694 16870694 + Missense_Mutation SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chrX:16870694G>A c.943C>T c.(943-945)Cat>Tat p.H315Y

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 X 16887288 16887288 single base substitution C T 5_prime_UTR_variant BLCA-CN X 16887288 16887288 single base substitution C T synonymous_variant K21K 63G>A BLCA-CN X 16887288 16887288 single base substitution C T synonymous_variant K24K 72G>A BLCA-CN X 16887288 16887288 single base substitution C T synonymous_variant K68K 204G>A BLCA-US X 16864054 16864054 single base substitution T A downstream_gene_variant BLCA-US X 16864054 16864054 single base substitution T A exon_variant BLCA-US X 16864054 16864054 single base substitution T A missense_variant H29L 86A>T BLCA-US X 16864054 16864054 single base substitution T A missense_variant H360L 1079A>T BLCA-US X 16864054 16864054 single base substitution T A missense_variant H369L 1106A>T BLCA-US X 16864054 16864054 single base substitution T A missense_variant H413L 1238A>T BRCA-EU X 16853395 16853395 single base substitution G A downstream_gene_variant BRCA-EU X 16854390 16854390 single base substitution A G downstream_gene_variant BRCA-EU X 16855305 16855305 single base substitution T C downstream_gene_variant BRCA-EU X 16855652 16855652 single base substitution G C downstream_gene_variant BRCA-EU X 16855668 16855668 single base substitution G C downstream_gene_variant BRCA-EU X 16857820 16857820 single base substitution C T downstream_gene_variant BRCA-EU X 16857820 16857820 single base substitution C T intron_variant BRCA-EU X 16859563 16859563 single base substitution G C downstream_gene_variant BRCA-EU X 16859563 16859563 single base substitution G C intron_variant BRCA-EU X 16860554 16860554 single base substitution G C downstream_gene_variant BRCA-EU X 16860554 16860554 single base substitution G C intron_variant BRCA-EU X 16860678 16860678 single base substitution A G downstream_gene_variant BRCA-EU X 16860678 16860678 single base substitution A G intron_variant BRCA-EU X 16861024 16861024 single base substitution C G downstream_gene_variant BRCA-EU X 16861024 16861024 single base substitution C G intron_variant BRCA-EU X 16862493 16862493 single base substitution C G 3_prime_UTR_variant BRCA-EU X 16862493 16862493 single base substitution C G downstream_gene_variant BRCA-EU X 16862493 16862493 single base substitution C G intron_variant BRCA-EU X 16862850 16862850 single base substitution A T 3_prime_UTR_variant BRCA-EU X 16862850 16862850 single base substitution A T downstream_gene_variant BRCA-EU X 16862850 16862850 single base substitution A T exon_variant BRCA-EU X 16862850 16862850 single base substitution A T intron_variant BRCA-EU X 16863590 16863590 single base substitution T G downstream_gene_variant BRCA-EU X 16863590 16863590 single base substitution T G intron_variant BRCA-EU X 16864579 16864579 single base substitution G T downstream_gene_variant BRCA-EU X 16864579 16864579 single base substitution G T exon_variant BRCA-EU X 16864579 16864579 single base substitution G T intron_variant BRCA-EU X 16865312 16865312 single base substitution C G downstream_gene_variant BRCA-EU X 16865312 16865312 single base substitution C G exon_variant BRCA-EU X 16865312 16865312 single base substitution C G intron_variant BRCA-EU X 16866052 16866052 deletion of <=200bp G - downstream_gene_variant BRCA-EU X 16866052 16866052 deletion of <=200bp G - exon_variant BRCA-EU X 16866052 16866052 deletion of <=200bp G - intron_variant BRCA-EU X 16866963 16866963 single base substitution C G downstream_gene_variant BRCA-EU X 16866963 16866963 single base substitution C G exon_variant BRCA-EU X 16866963 16866963 single base substitution C G intron_variant BRCA-EU X 16867286 16867286 single base substitution T C 3_prime_UTR_variant BRCA-EU X 16867286 16867286 single base substitution T C downstream_gene_variant BRCA-EU X 16867286 16867286 single base substitution T C exon_variant BRCA-EU X 16867286 16867286 single base substitution T C intron_variant BRCA-EU X 16867297 16867297 single base substitution C T 3_prime_UTR_variant BRCA-EU X 16867297 16867297 single base substitution C T downstream_gene_variant BRCA-EU X 16867297 16867297 single base substitution C T exon_variant BRCA-EU X 16867297 16867297 single base substitution C T intron_variant BRCA-EU X 16867719 16867719 single base substitution C T downstream_gene_variant BRCA-EU X 16867719 16867719 single base substitution C T intron_variant BRCA-EU X 16867739 16867739 single base substitution G C downstream_gene_variant BRCA-EU X 16867739 16867739 single base substitution G C intron_variant BRCA-EU X 16868005 16868005 deletion of <=200bp A - downstream_gene_variant BRCA-EU X 16868005 16868005 deletion of <=200bp A - intron_variant BRCA-EU X 16868393 16868393 single base substitution C G downstream_gene_variant BRCA-EU X 16868393 16868393 single base substitution C G intron_variant BRCA-EU X 16869020 16869020 single base substitution G A downstream_gene_variant BRCA-EU X 16869020 16869020 single base substitution G A intron_variant BRCA-EU X 16869155 16869155 single base substitution G A downstream_gene_variant BRCA-EU X 16869155 16869155 single base substitution G A intron_variant BRCA-EU X 16871267 16871267 single base substitution G C exon_variant BRCA-EU X 16871267 16871267 single base substitution G C intron_variant BRCA-EU X 16871267 16871267 single base substitution G C upstream_gene_variant BRCA-EU X 16871366 16871369 deletion of <=200bp TGAA - exon_variant BRCA-EU X 16871366 16871369 deletion of <=200bp TGAA - intron_variant BRCA-EU X 16871366 16871369 deletion of <=200bp TGAA - upstream_gene_variant BRCA-EU X 16871622 16871622 single base substitution C G exon_variant BRCA-EU X 16871622 16871622 single base substitution C G intron_variant BRCA-EU X 16871622 16871622 single base substitution C G upstream_gene_variant BRCA-EU X 16873266 16873266 single base substitution G A intron_variant BRCA-EU X 16873266 16873266 single base substitution G A upstream_gene_variant BRCA-EU X 16874862 16874862 single base substitution A C intron_variant BRCA-EU X 16874862 16874862 single base substitution A C upstream_gene_variant BRCA-EU X 16875611 16875611 single base substitution G C intron_variant BRCA-EU X 16875611 16875611 single base substitution G C upstream_gene_variant BRCA-EU X 16877009 16877009 single base substitution C G downstream_gene_variant BRCA-EU X 16877009 16877009 single base substitution C G intron_variant BRCA-EU X 16877009 16877009 single base substitution C G upstream_gene_variant BRCA-EU X 16877420 16877420 single base substitution G C downstream_gene_variant BRCA-EU X 16877420 16877420 single base substitution G C intron_variant BRCA-EU X 16877420 16877420 single base substitution G C upstream_gene_variant BRCA-EU X 16877443 16877443 single base substitution C T downstream_gene_variant BRCA-EU X 16877443 16877443 single base substitution C T intron_variant BRCA-EU X 16877443 16877443 single base substitution C T upstream_gene_variant BRCA-EU X 16877618 16877618 single base substitution C A downstream_gene_variant BRCA-EU X 16877618 16877618 single base substitution C A intron_variant BRCA-EU X 16877618 16877618 single base substitution C A upstream_gene_variant BRCA-EU X 16879275 16879275 single base substitution C T downstream_gene_variant BRCA-EU X 16879275 16879275 single base substitution C T intron_variant BRCA-EU X 16879275 16879275 single base substitution C T upstream_gene_variant BRCA-EU X 16879676 16879676 single base substitution G T downstream_gene_variant BRCA-EU X 16879676 16879676 single base substitution G T intron_variant BRCA-EU X 16879676 16879676 single base substitution G T upstream_gene_variant BRCA-EU X 16885141 16885141 single base substitution T A downstream_gene_variant BRCA-EU X 16885141 16885141 single base substitution T A intron_variant BRCA-EU X 16885141 16885141 single base substitution T A upstream_gene_variant BRCA-EU X 16886305 16886305 single base substitution C G downstream_gene_variant BRCA-EU X 16886305 16886305 single base substitution C G intron_variant BRCA-EU X 16886700 16886700 single base substitution C G downstream_gene_variant BRCA-EU X 16886700 16886700 single base substitution C G intron_variant BRCA-EU X 16887427 16887427 single base substitution C T intron_variant BRCA-EU X 16889154 16889154 single base substitution G A upstream_gene_variant BRCA-EU X 16889570 16889570 single base substitution G A upstream_gene_variant BRCA-EU X 16889725 16889725 deletion of <=200bp G - upstream_gene_variant BRCA-EU X 16891451 16891451 single base substitution G C upstream_gene_variant BRCA-EU X 16891480 16891480 single base substitution C A upstream_gene_variant BRCA-EU X 16891735 16891735 deletion of <=200bp T - upstream_gene_variant BRCA-EU X 16891817 16891817 single base substitution C G upstream_gene_variant BRCA-EU X 16892538 16892538 single base substitution A G upstream_gene_variant BRCA-EU X 16893327 16893327 single base substitution C T upstream_gene_variant BRCA-EU X 16893468 16893468 single base substitution A G upstream_gene_variant BRCA-FR X 16857820 16857820 single base substitution C T downstream_gene_variant BRCA-FR X 16857820 16857820 single base substitution C T intron_variant BRCA-FR X 16857989 16857989 single base substitution C T downstream_gene_variant BRCA-FR X 16857989 16857989 single base substitution C T intron_variant BRCA-FR X 16859563 16859563 single base substitution G C downstream_gene_variant BRCA-FR X 16859563 16859563 single base substitution G C intron_variant BRCA-FR X 16860509 16860509 single base substitution T C downstream_gene_variant BRCA-FR X 16860509 16860509 single base substitution T C intron_variant BRCA-FR X 16867297 16867297 single base substitution C T 3_prime_UTR_variant BRCA-FR X 16867297 16867297 single base substitution C T downstream_gene_variant BRCA-FR X 16867297 16867297 single base substitution C T exon_variant BRCA-FR X 16867297 16867297 single base substitution C T intron_variant BRCA-FR X 16868393 16868393 single base substitution C G downstream_gene_variant BRCA-FR X 16868393 16868393 single base substitution C G intron_variant BRCA-FR X 16877420 16877420 single base substitution G C downstream_gene_variant BRCA-FR X 16877420 16877420 single base substitution G C intron_variant BRCA-FR X 16877420 16877420 single base substitution G C upstream_gene_variant BRCA-FR X 16887427 16887427 single base substitution C T intron_variant BRCA-UK X 16869607 16869607 single base substitution C G downstream_gene_variant BRCA-UK X 16869607 16869607 single base substitution C G intron_variant BRCA-UK X 16871267 16871267 single base substitution G C exon_variant BRCA-UK X 16871267 16871267 single base substitution G C intron_variant BRCA-UK X 16871267 16871267 single base substitution G C upstream_gene_variant BRCA-US X 16859739 16859739 single base substitution C T downstream_gene_variant BRCA-US X 16859739 16859739 single base substitution C T intron_variant BRCA-US X 16860134 16860134 single base substitution T C downstream_gene_variant BRCA-US X 16860134 16860134 single base substitution T C intron_variant BRCA-US X 16863181 16863181 single base substitution C T downstream_gene_variant BRCA-US X 16863181 16863181 single base substitution C T exon_variant BRCA-US X 16863181 16863181 single base substitution C T missense_variant E410K 1228G>A BRCA-US X 16863181 16863181 single base substitution C T missense_variant E419K 1255G>A BRCA-US X 16863181 16863181 single base substitution C T missense_variant E463K 1387G>A BRCA-US X 16863181 16863181 single base substitution C T missense_variant E79K 235G>A BRCA-US X 16863950 16863950 single base substitution C A downstream_gene_variant BRCA-US X 16863950 16863950 single base substitution C A splice_donor_variant BRCA-US X 16871848 16871848 single base substitution C G exon_variant BRCA-US X 16871848 16871848 single base substitution C G missense_variant E159Q 475G>C BRCA-US X 16871848 16871848 single base substitution C G missense_variant E230Q 688G>C BRCA-US X 16871848 16871848 single base substitution C G missense_variant E239Q 715G>C BRCA-US X 16871848 16871848 single base substitution C G missense_variant E283Q 847G>C BRCA-US X 16871848 16871848 single base substitution C G missense_variant E43Q 127G>C BRCA-US X 16871848 16871848 single base substitution C G upstream_gene_variant BRCA-US X 16887272 16887272 single base substitution G T 5_prime_UTR_variant BRCA-US X 16887272 16887272 single base substitution G T missense_variant L27I 79C>A BRCA-US X 16887272 16887272 single base substitution G T missense_variant L30I 88C>A BRCA-US X 16887272 16887272 single base substitution G T missense_variant L74I 220C>A BTCA-JP X 16859681 16859692 deletion of <=200bp CCATCAAAGCGG - downstream_gene_variant BTCA-JP X 16859681 16859692 deletion of <=200bp CCATCAAAGCGG - intron_variant BTCA-JP X 16872028 16872028 single base substitution T C intron_variant BTCA-JP X 16872028 16872028 single base substitution T C upstream_gene_variant BTCA-JP X 16875873 16875873 single base substitution C A intron_variant BTCA-JP X 16875873 16875873 single base substitution C A upstream_gene_variant BTCA-JP X 16887115 16887115 single base substitution T C downstream_gene_variant BTCA-JP X 16887115 16887115 single base substitution T C intron_variant BTCA-JP X 16887283 16887285 deletion of <=200bp TTC - 5_prime_UTR_variant BTCA-JP X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN22N BTCA-JP X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN25N BTCA-JP X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN69N CESC-US X 16859626 16859626 single base substitution C A downstream_gene_variant CESC-US X 16859626 16859626 single base substitution C A intron_variant CESC-US X 16870688 16870688 single base substitution C T exon_variant CESC-US X 16870688 16870688 single base substitution C T intron_variant CESC-US X 16870688 16870688 single base substitution C T missense_variant D121N 361G>A CESC-US X 16870688 16870688 single base substitution C T missense_variant D308N 922G>A CESC-US X 16870688 16870688 single base substitution C T missense_variant D317N 949G>A CESC-US X 16870688 16870688 single base substitution C T missense_variant D361N 1081G>A CESC-US X 16870688 16870688 single base substitution C T upstream_gene_variant CLLE-ES X 16893349 16893349 single base substitution G T upstream_gene_variant COAD-US X 16852426 16852426 single base substitution A C downstream_gene_variant COAD-US X 16859607 16859607 single base substitution G T downstream_gene_variant COAD-US X 16859607 16859607 single base substitution G T intron_variant COAD-US X 16859628 16859628 single base substitution G A downstream_gene_variant COAD-US X 16859628 16859628 single base substitution G A intron_variant COAD-US X 16864001 16864001 deletion of <=200bp A - downstream_gene_variant COAD-US X 16864001 16864001 deletion of <=200bp A - exon_variant COAD-US X 16864001 16864001 deletion of <=200bp A - frameshift_variant W378 COAD-US X 16864001 16864001 deletion of <=200bp A - frameshift_variant W387 COAD-US X 16864001 16864001 deletion of <=200bp A - frameshift_variant W431 COAD-US X 16864001 16864001 deletion of <=200bp A - frameshift_variant W47 COAD-US X 16870194 16870194 single base substitution G T downstream_gene_variant COAD-US X 16870194 16870194 single base substitution G T exon_variant COAD-US X 16870194 16870194 single base substitution G T missense_variant R143S 427C>A COAD-US X 16870194 16870194 single base substitution G T missense_variant R278S 832C>A COAD-US X 16870194 16870194 single base substitution G T missense_variant R330S 988C>A COAD-US X 16870194 16870194 single base substitution G T missense_variant R339S 1015C>A COAD-US X 16870194 16870194 single base substitution G T missense_variant R383S 1147C>A COAD-US X 16870194 16870194 single base substitution G T upstream_gene_variant COAD-US X 16870679 16870679 single base substitution A C exon_variant COAD-US X 16870679 16870679 single base substitution A C missense_variant F124V 370T>G COAD-US X 16870679 16870679 single base substitution A C missense_variant F311V 931T>G COAD-US X 16870679 16870679 single base substitution A C missense_variant F320V 958T>G COAD-US X 16870679 16870679 single base substitution A C missense_variant F364V 1090T>G COAD-US X 16870679 16870679 single base substitution A C splice_region_variant COAD-US X 16870679 16870679 single base substitution A C upstream_gene_variant COAD-US X 16876898 16876898 single base substitution G A downstream_gene_variant COAD-US X 16876898 16876898 single base substitution G A exon_variant COAD-US X 16876898 16876898 single base substitution G A missense_variant R119C 355C>T COAD-US X 16876898 16876898 single base substitution G A missense_variant R128C 382C>T COAD-US X 16876898 16876898 single base substitution G A missense_variant R172C 514C>T COAD-US X 16876898 16876898 single base substitution G A missense_variant R48C 142C>T COAD-US X 16876898 16876898 single base substitution G A upstream_gene_variant COAD-US X 16887283 16887285 deletion of <=200bp TTC - 5_prime_UTR_variant COAD-US X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN22N COAD-US X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN25N COAD-US X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN69N COAD-US X 16887317 16887317 single base substitution C T 5_prime_UTR_variant COAD-US X 16887317 16887317 single base substitution C T missense_variant V12I 34G>A COAD-US X 16887317 16887317 single base substitution C T missense_variant V15I 43G>A COAD-US X 16887317 16887317 single base substitution C T missense_variant V59I 175G>A COCA-CN X 16859482 16859482 single base substitution G A downstream_gene_variant COCA-CN X 16859482 16859482 single base substitution G A intron_variant COCA-CN X 16863174 16863174 single base substitution T G downstream_gene_variant COCA-CN X 16863174 16863174 single base substitution T G exon_variant COCA-CN X 16863174 16863174 single base substitution T G missense_variant E412A 1235A>C COCA-CN X 16863174 16863174 single base substitution T G missense_variant E421A 1262A>C COCA-CN X 16863174 16863174 single base substitution T G missense_variant E465A 1394A>C COCA-CN X 16863174 16863174 single base substitution T G missense_variant E81A 242A>C COCA-CN X 16864135 16864135 single base substitution T G downstream_gene_variant COCA-CN X 16864135 16864135 single base substitution T G exon_variant COCA-CN X 16864135 16864135 single base substitution T G intron_variant COCA-CN X 16870729 16870729 single base substitution C T exon_variant COCA-CN X 16870729 16870729 single base substitution C T intron_variant COCA-CN X 16870729 16870729 single base substitution C T missense_variant R107H 320G>A COCA-CN X 16870729 16870729 single base substitution C T missense_variant R294H 881G>A COCA-CN X 16870729 16870729 single base substitution C T missense_variant R303H 908G>A COCA-CN X 16870729 16870729 single base substitution C T missense_variant R347H 1040G>A COCA-CN X 16870729 16870729 single base substitution C T upstream_gene_variant COCA-CN X 16870866 16870866 single base substitution C T exon_variant COCA-CN X 16870866 16870866 single base substitution C T intron_variant COCA-CN X 16870866 16870866 single base substitution C T splice_region_variant COCA-CN X 16870866 16870866 single base substitution C T upstream_gene_variant COCA-CN X 16870937 16870937 single base substitution C T exon_variant COCA-CN X 16870937 16870937 single base substitution C T missense_variant E194K 580G>A COCA-CN X 16870937 16870937 single base substitution C T missense_variant E265K 793G>A COCA-CN X 16870937 16870937 single base substitution C T missense_variant E274K 820G>A COCA-CN X 16870937 16870937 single base substitution C T missense_variant E318K 952G>A COCA-CN X 16870937 16870937 single base substitution C T missense_variant E78K 232G>A COCA-CN X 16870937 16870937 single base substitution C T upstream_gene_variant COCA-CN X 16871891 16871891 single base substitution G A exon_variant COCA-CN X 16871891 16871891 single base substitution G A synonymous_variant G144G 432C>T COCA-CN X 16871891 16871891 single base substitution G A synonymous_variant G215G 645C>T COCA-CN X 16871891 16871891 single base substitution G A synonymous_variant G224G 672C>T COCA-CN X 16871891 16871891 single base substitution G A synonymous_variant G268G 804C>T COCA-CN X 16871891 16871891 single base substitution G A synonymous_variant G28G 84C>T COCA-CN X 16871891 16871891 single base substitution G A upstream_gene_variant COCA-CN X 16873160 16873160 single base substitution G T intron_variant COCA-CN X 16873160 16873160 single base substitution G T upstream_gene_variant COCA-CN X 16875702 16875702 single base substitution G T intron_variant COCA-CN X 16875702 16875702 single base substitution G T upstream_gene_variant EOPC-DE X 16857990 16857990 single base substitution G A downstream_gene_variant EOPC-DE X 16857990 16857990 single base substitution G A intron_variant ESCA-CN X 16887273 16887273 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN X 16887273 16887273 single base substitution A C missense_variant F26L 78T>G ESCA-CN X 16887273 16887273 single base substitution A C missense_variant F29L 87T>G ESCA-CN X 16887273 16887273 single base substitution A C missense_variant F73L 219T>G KIRP-US X 16864059 16864059 single base substitution A G downstream_gene_variant KIRP-US X 16864059 16864059 single base substitution A G exon_variant KIRP-US X 16864059 16864059 single base substitution A G splice_region_variant LGG-US X 16887194 16887197 deletion of <=200bp CTTA - downstream_gene_variant LGG-US X 16887194 16887197 deletion of <=200bp CTTA - splice_donor_variant LICA-CN X 16887237 16887237 single base substitution C G downstream_gene_variant LICA-CN X 16887237 16887237 single base substitution C G missense_variant W41C 123G>C LICA-CN X 16887237 16887237 single base substitution C G missense_variant W7C 21G>C LICA-CN X 16887237 16887237 single base substitution C G missense_variant W85C 255G>C LINC-JP X 16852434 16852434 single base substitution A G downstream_gene_variant LINC-JP X 16858113 16858113 single base substitution C T downstream_gene_variant LINC-JP X 16858113 16858113 single base substitution C T intron_variant LINC-JP X 16864075 16864075 deletion of <=200bp A - downstream_gene_variant LINC-JP X 16864075 16864075 deletion of <=200bp A - exon_variant LINC-JP X 16864075 16864075 deletion of <=200bp A - intron_variant LINC-JP X 16870915 16870915 single base substitution T C exon_variant LINC-JP X 16870915 16870915 single base substitution T C missense_variant N201S 602A>G LINC-JP X 16870915 16870915 single base substitution T C missense_variant N272S 815A>G LINC-JP X 16870915 16870915 single base substitution T C missense_variant N281S 842A>G LINC-JP X 16870915 16870915 single base substitution T C missense_variant N325S 974A>G LINC-JP X 16870915 16870915 single base substitution T C missense_variant N85S 254A>G LINC-JP X 16870915 16870915 single base substitution T C upstream_gene_variant LINC-JP X 16871713 16871713 deletion of <=200bp A - exon_variant LINC-JP X 16871713 16871713 deletion of <=200bp A - intron_variant LINC-JP X 16871713 16871713 deletion of <=200bp A - upstream_gene_variant LINC-JP X 16871980 16871980 single base substitution G C intron_variant LINC-JP X 16871980 16871980 single base substitution G C upstream_gene_variant LINC-JP X 16871993 16871993 single base substitution G A intron_variant LINC-JP X 16871993 16871993 single base substitution G A upstream_gene_variant LINC-JP X 16872028 16872028 single base substitution T C intron_variant LINC-JP X 16872028 16872028 single base substitution T C upstream_gene_variant LINC-JP X 16883217 16883217 single base substitution T A downstream_gene_variant LINC-JP X 16883217 16883217 single base substitution T A intron_variant LINC-JP X 16883217 16883217 single base substitution T A upstream_gene_variant LINC-JP X 16883532 16883532 single base substitution G T downstream_gene_variant LINC-JP X 16883532 16883532 single base substitution G T intron_variant LINC-JP X 16883532 16883532 single base substitution G T upstream_gene_variant LINC-JP X 16884422 16884422 single base substitution G A downstream_gene_variant LINC-JP X 16884422 16884422 single base substitution G A intron_variant LINC-JP X 16884422 16884422 single base substitution G A upstream_gene_variant LINC-JP X 16887218 16887218 single base substitution A G downstream_gene_variant LINC-JP X 16887218 16887218 single base substitution A G missense_variant W14R 40T>C LINC-JP X 16887218 16887218 single base substitution A G missense_variant W48R 142T>C LINC-JP X 16887218 16887218 single base substitution A G missense_variant W92R 274T>C LIRI-JP X 16860044 16860044 single base substitution T G downstream_gene_variant LIRI-JP X 16860044 16860044 single base substitution T G intron_variant LIRI-JP X 16860052 16860052 single base substitution T G downstream_gene_variant LIRI-JP X 16860052 16860052 single base substitution T G intron_variant LIRI-JP X 16862022 16862022 single base substitution A C downstream_gene_variant LIRI-JP X 16862022 16862022 single base substitution A C intron_variant LIRI-JP X 16863237 16863237 deletion of <=200bp C - downstream_gene_variant LIRI-JP X 16863237 16863237 deletion of <=200bp C - intron_variant LIRI-JP X 16865083 16865083 single base substitution C A downstream_gene_variant LIRI-JP X 16865083 16865083 single base substitution C A exon_variant LIRI-JP X 16865083 16865083 single base substitution C A intron_variant LIRI-JP X 16872794 16872794 single base substitution C T intron_variant LIRI-JP X 16872794 16872794 single base substitution C T upstream_gene_variant LIRI-JP X 16877031 16877031 single base substitution C G downstream_gene_variant LIRI-JP X 16877031 16877031 single base substitution C G intron_variant LIRI-JP X 16877031 16877031 single base substitution C G upstream_gene_variant LIRI-JP X 16877311 16877311 single base substitution T A downstream_gene_variant LIRI-JP X 16877311 16877311 single base substitution T A intron_variant LIRI-JP X 16877311 16877311 single base substitution T A upstream_gene_variant LIRI-JP X 16877580 16877580 single base substitution T C downstream_gene_variant LIRI-JP X 16877580 16877580 single base substitution T C intron_variant LIRI-JP X 16877580 16877580 single base substitution T C upstream_gene_variant LIRI-JP X 16882006 16882006 single base substitution T C intron_variant LIRI-JP X 16882006 16882006 single base substitution T C upstream_gene_variant LIRI-JP X 16884425 16884425 single base substitution C T downstream_gene_variant LIRI-JP X 16884425 16884425 single base substitution C T intron_variant LIRI-JP X 16884425 16884425 single base substitution C T upstream_gene_variant LIRI-JP X 16886061 16886061 single base substitution G A downstream_gene_variant LIRI-JP X 16886061 16886061 single base substitution G A intron_variant LIRI-JP X 16886061 16886061 single base substitution G A upstream_gene_variant LIRI-JP X 16886229 16886229 single base substitution C A downstream_gene_variant LIRI-JP X 16886229 16886229 single base substitution C A intron_variant LIRI-JP X 16886619 16886619 single base substitution T C downstream_gene_variant LIRI-JP X 16886619 16886619 single base substitution T C intron_variant LIRI-JP X 16888932 16888932 single base substitution G T upstream_gene_variant LIRI-JP X 16889588 16889588 single base substitution C T upstream_gene_variant LUSC-KR X 16860134 16860134 single base substitution T C downstream_gene_variant LUSC-KR X 16860134 16860134 single base substitution T C intron_variant LUSC-KR X 16880993 16880993 single base substitution A G downstream_gene_variant LUSC-KR X 16880993 16880993 single base substitution A G intron_variant LUSC-KR X 16880993 16880993 single base substitution A G upstream_gene_variant LUSC-KR X 16881201 16881201 single base substitution G A missense_variant L106F 316C>T LUSC-KR X 16881201 16881201 single base substitution G A missense_variant L28F 82C>T LUSC-KR X 16881201 16881201 single base substitution G A missense_variant L62F 184C>T LUSC-KR X 16881201 16881201 single base substitution G A upstream_gene_variant LUSC-KR X 16890088 16890088 single base substitution C A upstream_gene_variant LUSC-US X 16858001 16858001 single base substitution G T downstream_gene_variant LUSC-US X 16858001 16858001 single base substitution G T intron_variant LUSC-US X 16881153 16881153 single base substitution G A synonymous_variant L122L 364C>T LUSC-US X 16881153 16881153 single base substitution G A synonymous_variant L44L 130C>T LUSC-US X 16881153 16881153 single base substitution G A synonymous_variant L78L 232C>T LUSC-US X 16881153 16881153 single base substitution G A upstream_gene_variant MALY-DE X 16859377 16859377 single base substitution C T downstream_gene_variant MALY-DE X 16859377 16859377 single base substitution C T intron_variant MALY-DE X 16876400 16876400 single base substitution C T downstream_gene_variant MALY-DE X 16876400 16876400 single base substitution C T intron_variant MALY-DE X 16876400 16876400 single base substitution C T upstream_gene_variant MALY-DE X 16880671 16880671 single base substitution A T downstream_gene_variant MALY-DE X 16880671 16880671 single base substitution A T intron_variant MALY-DE X 16880671 16880671 single base substitution A T upstream_gene_variant MALY-DE X 16882277 16882278 deletion of <=200bp AC - downstream_gene_variant MALY-DE X 16882277 16882278 deletion of <=200bp AC - intron_variant MALY-DE X 16882277 16882278 deletion of <=200bp AC - upstream_gene_variant MALY-DE X 16886894 16886894 single base substitution A C downstream_gene_variant MALY-DE X 16886894 16886894 single base substitution A C intron_variant MALY-DE X 16887153 16887153 single base substitution A G downstream_gene_variant MALY-DE X 16887153 16887153 single base substitution A G intron_variant MALY-DE X 16887162 16887162 single base substitution A G downstream_gene_variant MALY-DE X 16887162 16887162 single base substitution A G intron_variant MELA-AU X 16852721 16852721 single base substitution G A downstream_gene_variant MELA-AU X 16854273 16854273 single base substitution C T downstream_gene_variant MELA-AU X 16855629 16855629 single base substitution A G downstream_gene_variant MELA-AU X 16856263 16856263 single base substitution C T downstream_gene_variant MELA-AU X 16857704 16857704 single base substitution A G downstream_gene_variant MELA-AU X 16857704 16857704 single base substitution A G intron_variant MELA-AU X 16858566 16858566 single base substitution A G downstream_gene_variant MELA-AU X 16858566 16858566 single base substitution A G intron_variant MELA-AU X 16859502 16859502 single base substitution A G downstream_gene_variant MELA-AU X 16859502 16859502 single base substitution A G intron_variant MELA-AU X 16859516 16859516 single base substitution T C downstream_gene_variant MELA-AU X 16859516 16859516 single base substitution T C intron_variant MELA-AU X 16859926 16859926 single base substitution G A downstream_gene_variant MELA-AU X 16859926 16859926 single base substitution G A intron_variant MELA-AU X 16860038 16860038 single base substitution G A downstream_gene_variant MELA-AU X 16860038 16860038 single base substitution G A intron_variant MELA-AU X 16860143 16860143 single base substitution C T downstream_gene_variant MELA-AU X 16860143 16860143 single base substitution C T intron_variant MELA-AU X 16861423 16861423 single base substitution G A downstream_gene_variant MELA-AU X 16861423 16861423 single base substitution G A intron_variant MELA-AU X 16862012 16862012 single base substitution G A downstream_gene_variant MELA-AU X 16862012 16862012 single base substitution G A intron_variant MELA-AU X 16862699 16862699 single base substitution T C 3_prime_UTR_variant MELA-AU X 16862699 16862699 single base substitution T C downstream_gene_variant MELA-AU X 16862699 16862699 single base substitution T C intron_variant MELA-AU X 16862924 16862924 single base substitution C T 3_prime_UTR_variant MELA-AU X 16862924 16862924 single base substitution C T downstream_gene_variant MELA-AU X 16862924 16862924 single base substitution C T exon_variant MELA-AU X 16862924 16862924 single base substitution C T intron_variant MELA-AU X 16863872 16863872 single base substitution G A downstream_gene_variant MELA-AU X 16863872 16863872 single base substitution G A intron_variant MELA-AU X 16865177 16865177 single base substitution G A downstream_gene_variant MELA-AU X 16865177 16865177 single base substitution G A exon_variant MELA-AU X 16865177 16865177 single base substitution G A intron_variant MELA-AU X 16866830 16866830 single base substitution G A downstream_gene_variant MELA-AU X 16866830 16866830 single base substitution G A exon_variant MELA-AU X 16866830 16866830 single base substitution G A intron_variant MELA-AU X 16866990 16866990 single base substitution G A downstream_gene_variant MELA-AU X 16866990 16866990 single base substitution G A exon_variant MELA-AU X 16866990 16866990 single base substitution G A intron_variant MELA-AU X 16867007 16867007 single base substitution G A downstream_gene_variant MELA-AU X 16867007 16867007 single base substitution G A exon_variant MELA-AU X 16867007 16867007 single base substitution G A intron_variant MELA-AU X 16869352 16869352 single base substitution A T downstream_gene_variant MELA-AU X 16869352 16869352 single base substitution A T intron_variant MELA-AU X 16869618 16869618 single base substitution G A downstream_gene_variant MELA-AU X 16869618 16869618 single base substitution G A intron_variant MELA-AU X 16869857 16869857 single base substitution T C downstream_gene_variant MELA-AU X 16869857 16869857 single base substitution T C intron_variant MELA-AU X 16870867 16870867 single base substitution G A exon_variant MELA-AU X 16870867 16870867 single base substitution G A intron_variant MELA-AU X 16870867 16870867 single base substitution G A splice_region_variant MELA-AU X 16870867 16870867 single base substitution G A upstream_gene_variant MELA-AU X 16871552 16871553 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU X 16871552 16871553 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 16871552 16871553 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 16872088 16872088 single base substitution C T intron_variant MELA-AU X 16872088 16872088 single base substitution C T upstream_gene_variant MELA-AU X 16872999 16872999 single base substitution G T intron_variant MELA-AU X 16872999 16872999 single base substitution G T upstream_gene_variant MELA-AU X 16874288 16874288 single base substitution G A intron_variant MELA-AU X 16874288 16874288 single base substitution G A upstream_gene_variant MELA-AU X 16874472 16874472 single base substitution G A intron_variant MELA-AU X 16874472 16874472 single base substitution G A upstream_gene_variant MELA-AU X 16875481 16875481 single base substitution G A intron_variant MELA-AU X 16875481 16875481 single base substitution G A upstream_gene_variant MELA-AU X 16878641 16878641 single base substitution C T downstream_gene_variant MELA-AU X 16878641 16878641 single base substitution C T intron_variant MELA-AU X 16878641 16878641 single base substitution C T upstream_gene_variant MELA-AU X 16878821 16878821 single base substitution A G downstream_gene_variant MELA-AU X 16878821 16878821 single base substitution A G intron_variant MELA-AU X 16878821 16878821 single base substitution A G upstream_gene_variant MELA-AU X 16880971 16880971 single base substitution G A downstream_gene_variant MELA-AU X 16880971 16880971 single base substitution G A intron_variant MELA-AU X 16880971 16880971 single base substitution G A upstream_gene_variant MELA-AU X 16881496 16881496 single base substitution T C intron_variant MELA-AU X 16881496 16881496 single base substitution T C upstream_gene_variant MELA-AU X 16881533 16881533 single base substitution G A intron_variant MELA-AU X 16881533 16881533 single base substitution G A upstream_gene_variant MELA-AU X 16882143 16882143 single base substitution G A intron_variant MELA-AU X 16882143 16882143 single base substitution G A upstream_gene_variant MELA-AU X 16882207 16882207 single base substitution A G intron_variant MELA-AU X 16882207 16882207 single base substitution A G upstream_gene_variant MELA-AU X 16882567 16882567 single base substitution G C downstream_gene_variant MELA-AU X 16882567 16882567 single base substitution G C intron_variant MELA-AU X 16882567 16882567 single base substitution G C upstream_gene_variant MELA-AU X 16885477 16885478 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU X 16885477 16885478 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 16885477 16885478 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU X 16886743 16886743 single base substitution T A downstream_gene_variant MELA-AU X 16886743 16886743 single base substitution T A intron_variant MELA-AU X 16887579 16887579 single base substitution G A intron_variant MELA-AU X 16888590 16888591 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 16890435 16890435 single base substitution C T upstream_gene_variant MELA-AU X 16890854 16890855 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 16891745 16891745 single base substitution A G upstream_gene_variant MELA-AU X 16893274 16893274 single base substitution C T upstream_gene_variant MELA-AU X 16893404 16893404 single base substitution T C upstream_gene_variant MELA-AU X 16893498 16893498 single base substitution C T upstream_gene_variant ORCA-IN X 16859697 16859697 single base substitution C G downstream_gene_variant ORCA-IN X 16859697 16859697 single base substitution C G intron_variant ORCA-IN X 16862141 16862141 single base substitution G A downstream_gene_variant ORCA-IN X 16862141 16862141 single base substitution G A intron_variant ORCA-IN X 16863304 16863304 single base substitution T C downstream_gene_variant ORCA-IN X 16863304 16863304 single base substitution T C intron_variant ORCA-IN X 16870999 16870999 single base substitution C T exon_variant ORCA-IN X 16870999 16870999 single base substitution C T splice_acceptor_variant ORCA-IN X 16870999 16870999 single base substitution C T upstream_gene_variant OV-AU X 16856541 16856541 single base substitution A G downstream_gene_variant OV-AU X 16856922 16856922 single base substitution C T downstream_gene_variant OV-AU X 16876018 16876018 single base substitution A G intron_variant OV-AU X 16876018 16876018 single base substitution A G upstream_gene_variant OV-AU X 16887419 16887419 single base substitution T A intron_variant PACA-AU X 16864095 16864095 single base substitution A G downstream_gene_variant PACA-AU X 16864095 16864095 single base substitution A G exon_variant PACA-AU X 16864095 16864095 single base substitution A G intron_variant PACA-AU X 16869003 16869003 single base substitution C A downstream_gene_variant PACA-AU X 16869003 16869003 single base substitution C A intron_variant PACA-AU X 16870170 16870170 single base substitution T A downstream_gene_variant PACA-AU X 16870170 16870170 single base substitution T A missense_variant S151C 451A>T PACA-AU X 16870170 16870170 single base substitution T A missense_variant S338C 1012A>T PACA-AU X 16870170 16870170 single base substitution T A missense_variant S347C 1039A>T PACA-AU X 16870170 16870170 single base substitution T A missense_variant S391C 1171A>T PACA-AU X 16870170 16870170 single base substitution T A missense_variant S7C 19A>T PACA-AU X 16870170 16870170 single base substitution T A splice_region_variant PACA-AU X 16870170 16870170 single base substitution T A synonymous_variant ?286 PACA-AU X 16870729 16870729 single base substitution C T exon_variant PACA-AU X 16870729 16870729 single base substitution C T intron_variant PACA-AU X 16870729 16870729 single base substitution C T missense_variant R107H 320G>A PACA-AU X 16870729 16870729 single base substitution C T missense_variant R294H 881G>A PACA-AU X 16870729 16870729 single base substitution C T missense_variant R303H 908G>A PACA-AU X 16870729 16870729 single base substitution C T missense_variant R347H 1040G>A PACA-AU X 16870729 16870729 single base substitution C T upstream_gene_variant PACA-AU X 16870879 16870879 single base substitution G A exon_variant PACA-AU X 16870879 16870879 single base substitution G A missense_variant A213V 638C>T PACA-AU X 16870879 16870879 single base substitution G A missense_variant A284V 851C>T PACA-AU X 16870879 16870879 single base substitution G A missense_variant A293V 878C>T PACA-AU X 16870879 16870879 single base substitution G A missense_variant A337V 1010C>T PACA-AU X 16870879 16870879 single base substitution G A missense_variant A97V 290C>T PACA-AU X 16870879 16870879 single base substitution G A upstream_gene_variant PACA-AU X 16879913 16879913 single base substitution C T downstream_gene_variant PACA-AU X 16879913 16879913 single base substitution C T intron_variant PACA-AU X 16879913 16879913 single base substitution C T upstream_gene_variant PACA-AU X 16881429 16881429 single base substitution G A intron_variant PACA-AU X 16881429 16881429 single base substitution G A upstream_gene_variant PACA-CA X 16856606 16856606 single base substitution A C downstream_gene_variant PACA-CA X 16858067 16858067 single base substitution T A downstream_gene_variant PACA-CA X 16858067 16858067 single base substitution T A intron_variant PACA-CA X 16861616 16861616 single base substitution A G downstream_gene_variant PACA-CA X 16861616 16861616 single base substitution A G intron_variant PACA-CA X 16862096 16862096 single base substitution A G downstream_gene_variant PACA-CA X 16862096 16862096 single base substitution A G intron_variant PACA-CA X 16878829 16878829 single base substitution A T downstream_gene_variant PACA-CA X 16878829 16878829 single base substitution A T intron_variant PACA-CA X 16878829 16878829 single base substitution A T upstream_gene_variant PACA-CA X 16880672 16880672 single base substitution T A downstream_gene_variant PACA-CA X 16880672 16880672 single base substitution T A intron_variant PACA-CA X 16880672 16880672 single base substitution T A upstream_gene_variant PACA-CA X 16885141 16885141 single base substitution T A downstream_gene_variant PACA-CA X 16885141 16885141 single base substitution T A intron_variant PACA-CA X 16885141 16885141 single base substitution T A upstream_gene_variant PACA-CA X 16890436 16890436 single base substitution A G upstream_gene_variant PAEN-IT X 16876283 16876283 single base substitution C G downstream_gene_variant PAEN-IT X 16876283 16876283 single base substitution C G intron_variant PAEN-IT X 16876283 16876283 single base substitution C G upstream_gene_variant PAEN-IT X 16877741 16877741 single base substitution A C downstream_gene_variant PAEN-IT X 16877741 16877741 single base substitution A C intron_variant PAEN-IT X 16877741 16877741 single base substitution A C upstream_gene_variant PBCA-DE X 16853651 16853651 single base substitution G A downstream_gene_variant PBCA-DE X 16866410 16866410 single base substitution C A downstream_gene_variant PBCA-DE X 16866410 16866410 single base substitution C A exon_variant PBCA-DE X 16866410 16866410 single base substitution C A intron_variant PBCA-DE X 16866505 16866505 single base substitution T C downstream_gene_variant PBCA-DE X 16866505 16866505 single base substitution T C exon_variant PBCA-DE X 16866505 16866505 single base substitution T C intron_variant PBCA-DE X 16877644 16877644 single base substitution T A downstream_gene_variant PBCA-DE X 16877644 16877644 single base substitution T A intron_variant PBCA-DE X 16877644 16877644 single base substitution T A upstream_gene_variant PBCA-DE X 16880988 16880988 single base substitution C T downstream_gene_variant PBCA-DE X 16880988 16880988 single base substitution C T intron_variant PBCA-DE X 16880988 16880988 single base substitution C T upstream_gene_variant PBCA-DE X 16882150 16882150 deletion of <=200bp T - intron_variant PBCA-DE X 16882150 16882150 deletion of <=200bp T - upstream_gene_variant PBCA-DE X 16889421 16889421 single base substitution G T upstream_gene_variant PRAD-CA X 16857969 16857969 single base substitution A G downstream_gene_variant PRAD-CA X 16857969 16857969 single base substitution A G intron_variant PRAD-CA X 16858560 16858560 single base substitution C A downstream_gene_variant PRAD-CA X 16858560 16858560 single base substitution C A intron_variant PRAD-CA X 16875487 16875487 single base substitution T C intron_variant PRAD-CA X 16875487 16875487 single base substitution T C upstream_gene_variant PRAD-CA X 16878808 16878808 single base substitution G A downstream_gene_variant PRAD-CA X 16878808 16878808 single base substitution G A intron_variant PRAD-CA X 16878808 16878808 single base substitution G A upstream_gene_variant PRAD-CA X 16893306 16893306 single base substitution G A upstream_gene_variant PRAD-US X 16859875 16859875 single base substitution G C downstream_gene_variant PRAD-US X 16859875 16859875 single base substitution G C intron_variant READ-US X 16863214 16863214 single base substitution A C downstream_gene_variant READ-US X 16863214 16863214 single base substitution A C exon_variant READ-US X 16863214 16863214 single base substitution A C missense_variant Y399D 1195T>G READ-US X 16863214 16863214 single base substitution A C missense_variant Y408D 1222T>G READ-US X 16863214 16863214 single base substitution A C missense_variant Y452D 1354T>G READ-US X 16863214 16863214 single base substitution A C missense_variant Y68D 202T>G READ-US X 16864060 16864060 single base substitution A C downstream_gene_variant READ-US X 16864060 16864060 single base substitution A C exon_variant READ-US X 16864060 16864060 single base substitution A C missense_variant F27C 80T>G READ-US X 16864060 16864060 single base substitution A C missense_variant F358C 1073T>G READ-US X 16864060 16864060 single base substitution A C missense_variant F367C 1100T>G READ-US X 16864060 16864060 single base substitution A C missense_variant F411C 1232T>G READ-US X 16864060 16864060 single base substitution A C splice_region_variant READ-US X 16870190 16870190 single base substitution C T downstream_gene_variant READ-US X 16870190 16870190 single base substitution C T exon_variant READ-US X 16870190 16870190 single base substitution C T missense_variant R144H 431G>A READ-US X 16870190 16870190 single base substitution C T missense_variant R279H 836G>A READ-US X 16870190 16870190 single base substitution C T missense_variant R331H 992G>A READ-US X 16870190 16870190 single base substitution C T missense_variant R340H 1019G>A READ-US X 16870190 16870190 single base substitution C T missense_variant R384H 1151G>A READ-US X 16870190 16870190 single base substitution C T upstream_gene_variant RECA-EU X 16864130 16864130 single base substitution A C downstream_gene_variant RECA-EU X 16864130 16864130 single base substitution A C exon_variant RECA-EU X 16864130 16864130 single base substitution A C intron_variant RECA-EU X 16874900 16874900 single base substitution T C intron_variant RECA-EU X 16874900 16874900 single base substitution T C upstream_gene_variant RECA-EU X 16883216 16883216 single base substitution A G downstream_gene_variant RECA-EU X 16883216 16883216 single base substitution A G intron_variant RECA-EU X 16883216 16883216 single base substitution A G upstream_gene_variant SKCA-BR X 16855920 16855920 single base substitution C T downstream_gene_variant SKCA-BR X 16856630 16856630 single base substitution C T downstream_gene_variant SKCA-BR X 16859279 16859279 single base substitution T C downstream_gene_variant SKCA-BR X 16859279 16859279 single base substitution T C intron_variant SKCA-BR X 16859970 16859970 single base substitution G A downstream_gene_variant SKCA-BR X 16859970 16859970 single base substitution G A intron_variant SKCA-BR X 16860011 16860011 single base substitution G A downstream_gene_variant SKCA-BR X 16860011 16860011 single base substitution G A intron_variant SKCA-BR X 16865111 16865111 single base substitution G A downstream_gene_variant SKCA-BR X 16865111 16865111 single base substitution G A exon_variant SKCA-BR X 16865111 16865111 single base substitution G A intron_variant SKCA-BR X 16870913 16870913 single base substitution G A exon_variant SKCA-BR X 16870913 16870913 single base substitution G A missense_variant P202S 604C>T SKCA-BR X 16870913 16870913 single base substitution G A missense_variant P273S 817C>T SKCA-BR X 16870913 16870913 single base substitution G A missense_variant P282S 844C>T SKCA-BR X 16870913 16870913 single base substitution G A missense_variant P326S 976C>T SKCA-BR X 16870913 16870913 single base substitution G A missense_variant P86S 256C>T SKCA-BR X 16870913 16870913 single base substitution G A upstream_gene_variant SKCA-BR X 16873094 16873094 single base substitution C T intron_variant SKCA-BR X 16873094 16873094 single base substitution C T upstream_gene_variant SKCA-BR X 16882663 16882671 deletion of <=200bp AAAAAAAAG - downstream_gene_variant SKCA-BR X 16882663 16882671 deletion of <=200bp AAAAAAAAG - intron_variant SKCA-BR X 16882663 16882671 deletion of <=200bp AAAAAAAAG - upstream_gene_variant SKCA-BR X 16882671 16882671 single base substitution G A downstream_gene_variant SKCA-BR X 16882671 16882671 single base substitution G A intron_variant SKCA-BR X 16882671 16882671 single base substitution G A upstream_gene_variant SKCA-BR X 16888709 16888709 single base substitution C T upstream_gene_variant SKCA-BR X 16888710 16888710 single base substitution C T upstream_gene_variant SKCM-US X 16870694 16870694 single base substitution G A exon_variant SKCM-US X 16870694 16870694 single base substitution G A intron_variant SKCM-US X 16870694 16870694 single base substitution G A missense_variant H119Y 355C>T SKCM-US X 16870694 16870694 single base substitution G A missense_variant H306Y 916C>T SKCM-US X 16870694 16870694 single base substitution G A missense_variant H315Y 943C>T SKCM-US X 16870694 16870694 single base substitution G A missense_variant H359Y 1075C>T SKCM-US X 16870694 16870694 single base substitution G A upstream_gene_variant STAD-US X 16857989 16857989 single base substitution C T downstream_gene_variant STAD-US X 16857989 16857989 single base substitution C T intron_variant STAD-US X 16859704 16859704 single base substitution G A downstream_gene_variant STAD-US X 16859704 16859704 single base substitution G A intron_variant STAD-US X 16859880 16859880 single base substitution G A downstream_gene_variant STAD-US X 16859880 16859880 single base substitution G A intron_variant STAD-US X 16870202 16870202 single base substitution C T downstream_gene_variant STAD-US X 16870202 16870202 single base substitution C T exon_variant STAD-US X 16870202 16870202 single base substitution C T missense_variant G140D 419G>A STAD-US X 16870202 16870202 single base substitution C T missense_variant G275D 824G>A STAD-US X 16870202 16870202 single base substitution C T missense_variant G327D 980G>A STAD-US X 16870202 16870202 single base substitution C T missense_variant G336D 1007G>A STAD-US X 16870202 16870202 single base substitution C T missense_variant G380D 1139G>A STAD-US X 16870202 16870202 single base substitution C T upstream_gene_variant STAD-US X 16870926 16870926 single base substitution G A exon_variant STAD-US X 16870926 16870926 single base substitution G A synonymous_variant C197C 591C>T STAD-US X 16870926 16870926 single base substitution G A synonymous_variant C268C 804C>T STAD-US X 16870926 16870926 single base substitution G A synonymous_variant C277C 831C>T STAD-US X 16870926 16870926 single base substitution G A synonymous_variant C321C 963C>T STAD-US X 16870926 16870926 single base substitution G A synonymous_variant C81C 243C>T STAD-US X 16870926 16870926 single base substitution G A upstream_gene_variant STAD-US X 16870931 16870931 single base substitution T G exon_variant STAD-US X 16870931 16870931 single base substitution T G missense_variant N196H 586A>C STAD-US X 16870931 16870931 single base substitution T G missense_variant N267H 799A>C STAD-US X 16870931 16870931 single base substitution T G missense_variant N276H 826A>C STAD-US X 16870931 16870931 single base substitution T G missense_variant N320H 958A>C STAD-US X 16870931 16870931 single base substitution T G missense_variant N80H 238A>C STAD-US X 16870931 16870931 single base substitution T G upstream_gene_variant STAD-US X 16870947 16870947 single base substitution C T exon_variant STAD-US X 16870947 16870947 single base substitution C T synonymous_variant A190A 570G>A STAD-US X 16870947 16870947 single base substitution C T synonymous_variant A261A 783G>A STAD-US X 16870947 16870947 single base substitution C T synonymous_variant A270A 810G>A STAD-US X 16870947 16870947 single base substitution C T synonymous_variant A314A 942G>A STAD-US X 16870947 16870947 single base substitution C T synonymous_variant A74A 222G>A STAD-US X 16870947 16870947 single base substitution C T upstream_gene_variant STAD-US X 16876853 16876853 deletion of <=200bp T - downstream_gene_variant STAD-US X 16876853 16876853 deletion of <=200bp T - exon_variant STAD-US X 16876853 16876853 deletion of <=200bp T - frameshift_variant T134 STAD-US X 16876853 16876853 deletion of <=200bp T - frameshift_variant T143 STAD-US X 16876853 16876853 deletion of <=200bp T - frameshift_variant T187 STAD-US X 16876853 16876853 deletion of <=200bp T - frameshift_variant T63 STAD-US X 16876853 16876853 deletion of <=200bp T - upstream_gene_variant STAD-US X 16876866 16876866 single base substitution G A downstream_gene_variant STAD-US X 16876866 16876866 single base substitution G A exon_variant STAD-US X 16876866 16876866 single base substitution G A synonymous_variant I129I 387C>T STAD-US X 16876866 16876866 single base substitution G A synonymous_variant I138I 414C>T STAD-US X 16876866 16876866 single base substitution G A synonymous_variant I182I 546C>T STAD-US X 16876866 16876866 single base substitution G A synonymous_variant I58I 174C>T STAD-US X 16876866 16876866 single base substitution G A upstream_gene_variant STAD-US X 16876898 16876898 single base substitution G A downstream_gene_variant STAD-US X 16876898 16876898 single base substitution G A exon_variant STAD-US X 16876898 16876898 single base substitution G A missense_variant R119C 355C>T STAD-US X 16876898 16876898 single base substitution G A missense_variant R128C 382C>T STAD-US X 16876898 16876898 single base substitution G A missense_variant R172C 514C>T STAD-US X 16876898 16876898 single base substitution G A missense_variant R48C 142C>T STAD-US X 16876898 16876898 single base substitution G A upstream_gene_variant STAD-US X 16887283 16887285 deletion of <=200bp TTC - 5_prime_UTR_variant STAD-US X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN22N STAD-US X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN25N STAD-US X 16887283 16887285 deletion of <=200bp TTC - disruptive_inframe_deletion KN69N THCA-SA X 16859628 16859628 single base substitution G A downstream_gene_variant THCA-SA X 16859628 16859628 single base substitution G A intron_variant THCA-SA X 16860134 16860134 single base substitution T C downstream_gene_variant THCA-SA X 16860134 16860134 single base substitution T C intron_variant UCEC-US X 16852420 16852420 single base substitution G A downstream_gene_variant UCEC-US X 16855743 16855743 single base substitution G T downstream_gene_variant UCEC-US X 16859599 16859599 single base substitution C T downstream_gene_variant UCEC-US X 16859599 16859599 single base substitution C T intron_variant UCEC-US X 16859706 16859706 single base substitution G A downstream_gene_variant UCEC-US X 16859706 16859706 single base substitution G A intron_variant UCEC-US X 16859706 16859706 single base substitution G T downstream_gene_variant UCEC-US X 16859706 16859706 single base substitution G T intron_variant UCEC-US X 16867363 16867363 single base substitution G A downstream_gene_variant UCEC-US X 16867363 16867363 single base substitution G A exon_variant UCEC-US X 16867363 16867363 single base substitution G A missense_variant R172C 514C>T UCEC-US X 16867363 16867363 single base substitution G A splice_region_variant UCEC-US X 16870185 16870185 single base substitution T G downstream_gene_variant UCEC-US X 16870185 16870185 single base substitution T G exon_variant UCEC-US X 16870185 16870185 single base substitution T G missense_variant N146H 436A>C UCEC-US X 16870185 16870185 single base substitution T G missense_variant N281H 841A>C UCEC-US X 16870185 16870185 single base substitution T G missense_variant N2H 4A>C UCEC-US X 16870185 16870185 single base substitution T G missense_variant N333H 997A>C UCEC-US X 16870185 16870185 single base substitution T G missense_variant N342H 1024A>C UCEC-US X 16870185 16870185 single base substitution T G missense_variant N386H 1156A>C UCEC-US X 16870696 16870696 single base substitution G T exon_variant UCEC-US X 16870696 16870696 single base substitution G T intron_variant UCEC-US X 16870696 16870696 single base substitution G T missense_variant S118Y 353C>A UCEC-US X 16870696 16870696 single base substitution G T missense_variant S305Y 914C>A UCEC-US X 16870696 16870696 single base substitution G T missense_variant S314Y 941C>A UCEC-US X 16870696 16870696 single base substitution G T missense_variant S358Y 1073C>A UCEC-US X 16870696 16870696 single base substitution G T upstream_gene_variant UCEC-US X 16871856 16871856 single base substitution A G exon_variant UCEC-US X 16871856 16871856 single base substitution A G missense_variant L156P 467T>C UCEC-US X 16871856 16871856 single base substitution A G missense_variant L227P 680T>C UCEC-US X 16871856 16871856 single base substitution A G missense_variant L236P 707T>C UCEC-US X 16871856 16871856 single base substitution A G missense_variant L280P 839T>C UCEC-US X 16871856 16871856 single base substitution A G missense_variant L40P 119T>C UCEC-US X 16871856 16871856 single base substitution A G upstream_gene_variant UCEC-US X 16871929 16871929 single base substitution C A exon_variant UCEC-US X 16871929 16871929 single base substitution C A stop_gained E132* 394G>T UCEC-US X 16871929 16871929 single base substitution C A stop_gained E16* 46G>T UCEC-US X 16871929 16871929 single base substitution C A stop_gained E203* 607G>T UCEC-US X 16871929 16871929 single base substitution C A stop_gained E212* 634G>T UCEC-US X 16871929 16871929 single base substitution C A stop_gained E256* 766G>T UCEC-US X 16871929 16871929 single base substitution C A upstream_gene_variant UCEC-US X 16871942 16871942 single base substitution G A exon_variant UCEC-US X 16871942 16871942 single base substitution G A synonymous_variant N11N 33C>T UCEC-US X 16871942 16871942 single base substitution G A synonymous_variant N127N 381C>T UCEC-US X 16871942 16871942 single base substitution G A synonymous_variant N198N 594C>T UCEC-US X 16871942 16871942 single base substitution G A synonymous_variant N207N 621C>T UCEC-US X 16871942 16871942 single base substitution G A synonymous_variant N251N 753C>T UCEC-US X 16871942 16871942 single base substitution G A upstream_gene_variant UCEC-US X 16871954 16871954 single base substitution C T exon_variant UCEC-US X 16871954 16871954 single base substitution C T synonymous_variant L123L 369G>A UCEC-US X 16871954 16871954 single base substitution C T synonymous_variant L194L 582G>A UCEC-US X 16871954 16871954 single base substitution C T synonymous_variant L203L 609G>A UCEC-US X 16871954 16871954 single base substitution C T synonymous_variant L247L 741G>A UCEC-US X 16871954 16871954 single base substitution C T synonymous_variant L7L 21G>A UCEC-US X 16871954 16871954 single base substitution C T upstream_gene_variant UCEC-US X 16875775 16875775 single base substitution T C exon_variant UCEC-US X 16875775 16875775 single base substitution T C missense_variant Y100C 299A>G UCEC-US X 16875775 16875775 single base substitution T C missense_variant Y171C 512A>G UCEC-US X 16875775 16875775 single base substitution T C missense_variant Y180C 539A>G UCEC-US X 16875775 16875775 single base substitution T C missense_variant Y224C 671A>G UCEC-US X 16875775 16875775 single base substitution T C upstream_gene_variant UCEC-US X 16875813 16875813 single base substitution A C exon_variant UCEC-US X 16875813 16875813 single base substitution A C missense_variant N158K 474T>G UCEC-US X 16875813 16875813 single base substitution A C missense_variant N167K 501T>G UCEC-US X 16875813 16875813 single base substitution A C missense_variant N211K 633T>G UCEC-US X 16875813 16875813 single base substitution A C missense_variant N87K 261T>G UCEC-US X 16875813 16875813 single base substitution A C upstream_gene_variant UCEC-US X 16876913 16876913 single base substitution C T downstream_gene_variant UCEC-US X 16876913 16876913 single base substitution C T exon_variant UCEC-US X 16876913 16876913 single base substitution C T missense_variant E114K 340G>A UCEC-US X 16876913 16876913 single base substitution C T missense_variant E123K 367G>A UCEC-US X 16876913 16876913 single base substitution C T missense_variant E167K 499G>A UCEC-US X 16876913 16876913 single base substitution C T missense_variant E43K 127G>A UCEC-US X 16876913 16876913 single base substitution C T upstream_gene_variant UCEC-US X 16887277 16887277 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US X 16887277 16887277 single base substitution G A missense_variant P25L 74C>T UCEC-US X 16887277 16887277 single base substitution G A missense_variant P28L 83C>T UCEC-US X 16887277 16887277 single base substitution G A missense_variant P72L 215C>T UCEC-US X 16887335 16887335 single base substitution C A 5_prime_UTR_variant UCEC-US X 16887335 16887335 single base substitution C A missense_variant D53Y 157G>T UCEC-US X 16887335 16887335 single base substitution C A missense_variant D6Y 16G>T UCEC-US X 16887335 16887335 single base substitution C A missense_variant D9Y 25G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AP-A056-01 COSM1118570 c.501T>G p.N167K Substitution - Missense 23:16857690-16857690 - YUKAT COSM5412375 c.637G>A p.G213S Substitution - Missense 23:16853803-16853803 - HCC6T COSM1625748 c.842A>G p.N281S Substitution - Missense 23:16852792-16852792 - LOVO COSM3035411 c.1254C>T p.S418S Substitution - coding silent 23:16845059-16845059 - PR-00-1165 COSM246965 c.384T>C p.R128R Substitution - coding silent 23:16858773-16858773 - TCGA-B5-A0JY-01 COSM1118573 c.25G>T p.D9Y Substitution - Missense 23:16869212-16869212 - TCGA-09-2051-01 COSM117170 c.889G>T p.V297L Substitution - Missense 23:16852625-16852625 - SS6003309 COSM3414261 c.17-8A>G p.? Unknown 23:16869228-16869228 - B66 COSM1756479 c.72G>A p.K24K Substitution - coding silent 23:16869165-16869165 - SNU-175 COSM181884 c.382C>T p.R128C Substitution - Missense 23:16858775-16858775 - TCGA-BR-A4QL-01 COSM4108375 c.831C>T p.C277C Substitution - coding silent 23:16852803-16852803 - 1017 COSM5730584 c.670G>A p.G224S Substitution - Missense 23:16853770-16853770 - TCGA-A6-2671-01 COSM1467014 c.1015C>A p.R339S Substitution - Missense 23:16852071-16852071 - ESCC_BICR_008T COSM5429009 c.87T>G p.F29L Substitution - Missense 23:16869150-16869150 - TCGA-EI-6917-01 COSM3424654 c.1100T>G p.F367C Substitution - Missense 23:16845937-16845937 - TCGA-10-0931-01 COSM80429 c.936C>T p.F312F Substitution - coding silent 23:16852578-16852578 - STC252 COSM5064568 c.590A>G p.D197G Substitution - Missense 23:16857601-16857601 - TCGA-AA-A01Q-01 COSM300111 c.1019G>A p.R340H Substitution - Missense 23:16852067-16852067 - W040 COSM308193 c.98_109del12 p.L33_T36delLVMT Deletion - In frame 23:16869128-16869139 - TCGA-D1-A17Q-01 COSM1118563 c.941C>A p.S314Y Substitution - Missense 23:16852573-16852573 - I2L-P7-Tumor-Organoid COSM5366755 c.1073_1081delCAGAAGATG p.A358_D360delAED Deletion - In frame 23:16849261-16849269 - T3202 COSM4720587 c.212C>T p.T71M Substitution - Missense 23:16863050-16863050 - TCGA-33-4547-01 COSM756688 c.232C>T p.L78L Substitution - coding silent 23:16863030-16863030 - SNU-175 COSM4650868 c.610T>C p.W204R Substitution - Missense 23:16853830-16853830 - TCGA-CG-5720-01 COSM181884 c.382C>T p.R128C Substitution - Missense 23:16858775-16858775 - BD6T COSM1467018 c.75_77delGAA p.K25delK Deletion - In frame 23:16869160-16869162 - TCGA-D1-A17Q-01 COSM1118571 c.367G>A p.E123K Substitution - Missense 23:16858790-16858790 - 90482 COSM329698 c.959delT p.F320fs*22 Deletion - Frameshift 23:16852555-16852555 - ESCC_33 COSM5628362 c.1111G>A p.G371R Substitution - Missense 23:16845926-16845926 - 8015858 COSM219021 c.908G>A p.R303H Substitution - Missense 23:16852606-16852606 - TCGA-CK-5916-01 COSM1467018 c.75_77delGAA p.K25delK Deletion - In frame 23:16869160-16869162 - T2269 COSM4720586 c.506A>C p.D169A Substitution - Missense 23:16857685-16857685 - I2L-P7-Tumor-Organoid COSM5367497 c.923A>G p.K308R Substitution - Missense 23:16852591-16852591 - TCGA-AC-A23C-01 COSM1490739 c.1209+1G>T p.? Unknown 23:16845827-16845827 - 8012346 COSM3390544 c.1039A>T p.S347C Substitution - Missense 23:16852047-16852047 - J88_T COSM3965009 c.184C>T p.L62F Substitution - Missense 23:16863078-16863078 - LUAD-E01278 COSM403537 c.520G>A p.G174S Substitution - Missense 23:16857671-16857671 - TCGA-BT-A2LB-01 COSM3800514 c.1106A>T p.H369L Substitution - Missense 23:16845931-16845931 - LUAD-NYU263 COSM372335 c.652G>T p.A218S Substitution - Missense 23:16853788-16853788 - TCGA-D1-A0ZO-01 COSM1118560 c.1132G>A p.D378N Substitution - Missense 23:16845905-16845905 - TCGA-CD-5798-01 COSM4108376 c.826A>C p.N276H Substitution - Missense 23:16852808-16852808 - Gp2D COSM300111 c.1019G>A p.R340H Substitution - Missense 23:16852067-16852067 - PR-09-5446 COSM246967 c.482-1G>C p.? Unknown 23:16857710-16857710 - 443 COSM4434800 c.1202G>A p.W401* Substitution - Nonsense 23:16845835-16845835 - TCGA-CA-6717-01 COSM181884 c.382C>T p.R128C Substitution - Missense 23:16858775-16858775 - TCGA-D1-A16Y-01 COSM1118567 c.621C>T p.N207N Substitution - coding silent 23:16853819-16853819 - B66-Tumor COSM1756479 c.72G>A p.K24K Substitution - coding silent 23:16869165-16869165 - TCGA-BP-4163-01 COSM488203 c.963+2T>C p.? Unknown 23:16852549-16852549 - OSCC-GB_01170111 COSM5954082 c.759-1G>A p.? Unknown 23:16852876-16852876 - TCGA-AZ-4315-01 COSM1467015 c.958T>G p.F320V Substitution - Missense 23:16852556-16852556 - TCGA-D3-A3C8-06 COSM3913711 c.943C>T p.H315Y Substitution - Missense 23:16852571-16852571 - ccRCC-92 COSM1663847 c.151G>A p.E51K Substitution - Missense 23:16869086-16869086 - Pat_59_A COSM5877531 c.967C>T p.H323Y Substitution - Missense 23:16852119-16852119 - T3091 COSM4720588 c.184C>A p.L62I Substitution - Missense 23:16863078-16863078 - TCGA-EI-6917-01 COSM3424653 c.1222T>G p.Y408D Substitution - Missense 23:16845091-16845091 - 9227_T COSM5041931 c.1098+1G>A p.? Unknown 23:16849243-16849243 - ICGC_0052 COSM219021 c.908G>A p.R303H Substitution - Missense 23:16852606-16852606 - TCGA-AN-A046-01 COSM3844199 c.1255G>A p.E419K Substitution - Missense 23:16845058-16845058 - EGC15 COSM5064567 c.853G>A p.E285K Substitution - Missense 23:16852781-16852781 - TCGA-BR-8487-01 COSM488204 c.810G>A p.A270A Substitution - coding silent 23:16852824-16852824 - SNU-C4 COSM4654544 c.625G>T p.G209* Substitution - Nonsense 23:16853815-16853815 - TCGA-AP-A059-01 COSM1118568 c.609G>A p.L203L Substitution - coding silent 23:16853831-16853831 - TCGA-AP-A056-01 COSM1118571 c.367G>A p.E123K Substitution - Missense 23:16858790-16858790 - BB30-HNC COSM25323 c.827A>G p.N276S Substitution - Missense 23:16852807-16852807 - TCGA-B5-A0K8-01 COSM1118564 c.781A>C p.T261P Substitution - Missense 23:16852853-16852853 - HCC71 COSM1625749 c.142T>C p.W48R Substitution - Missense 23:16869095-16869095 - TCGA-AD-5900-01 COSM1467019 c.43G>A p.V15I Substitution - Missense 23:16869194-16869194 - sysucc-274T COSM5476906 c.1262A>C p.E421A Substitution - Missense 23:16845051-16845051 - ICC009T COSM5823579 c.123G>C p.W41C Substitution - Missense 23:16869114-16869114 - 16617 COSM5617531 c.17-10C>T p.? Unknown 23:16869230-16869230 - TCGA-AA-3941-01 COSM296785 c.1247C>T p.T416M Substitution - Missense 23:16845066-16845066 - TCGA-AA-A010-01 COSM168298 c.937G>A p.E313K Substitution - Missense 23:16852577-16852577 - TCGA-BR-7957-01 COSM4108374 c.1007G>A p.G336D Substitution - Missense 23:16852079-16852079 - TCGA-CM-5861-01 COSM1467013 c.1159delT p.W387fs*>39 Deletion - Frameshift 23:16845878-16845878 - TCGA-G7-6793-01 COSM3992427 c.1101T>C p.F367F Substitution - coding silent 23:16845936-16845936 - Pat_16_B COSM1467017 c.809C>T p.A270V Substitution - Missense 23:16852825-16852825 - TCGA-BS-A0TE-01 COSM1118561 c.1098+4C>T p.? Unknown 23:16849240-16849240 - TCGA-A5-A0GB-01 COSM1118565 c.707T>C p.L236P Substitution - Missense 23:16853733-16853733 - LAU50_2 COSM233236 c.592G>A p.D198N Substitution - Missense 23:16857599-16857599 - S01542 COSM5669839 c.545T>C p.L182P Substitution - Missense 23:16857646-16857646 - TCGA-AN-A046-01 COSM3844200 c.88C>A p.L30I Substitution - Missense 23:16869149-16869149 - S01563 COSM314705 c.308-1G>T p.? Unknown 23:16858850-16858850 - ATL058 COSM181884 c.382C>T p.R128C Substitution - Missense 23:16858775-16858775 - TCGA-AP-A0LM-01 COSM1118572 c.83C>T p.P28L Substitution - Missense 23:16869154-16869154 - TCGA-CD-A48A-01 COSM4108377 c.414C>T p.I138I Substitution - coding silent 23:16858743-16858743 - 587376 COSM277022 c.820G>A p.E274K Substitution - Missense 23:16852814-16852814 - HCC71T COSM1625749 c.142T>C p.W48R Substitution - Missense 23:16869095-16869095 - TCGA-AA-A010-01 COSM277022 c.820G>A p.E274K Substitution - Missense 23:16852814-16852814 - 8058330 COSM3390545 c.878C>T p.A293V Substitution - Missense 23:16852756-16852756 - TCGA-AX-A05Z-01 COSM1118562 c.1024A>C p.N342H Substitution - Missense 23:16852062-16852062 - S01563 COSM314705 c.308-1G>T p.? Unknown 23:16858850-16858850 - Gp2D COSM4629005 c.764A>G p.D255G Substitution - Missense 23:16852870-16852870 - HCT116 COSM3035433 c.49A>G p.N17D Substitution - Missense 23:16869188-16869188 - PR-00-1165 COSM246966 c.1076A>G p.E359G Substitution - Missense 23:16849266-16849266 - PT49 COSM3913711 c.943C>T p.H315Y Substitution - Missense 23:16852571-16852571 - TCGA-BG-A0M3-01 COSM1118569 c.539A>G p.Y180C Substitution - Missense 23:16857652-16857652 - BB30-HNC COSM25323 c.827A>G p.N276S Substitution - Missense 23:16852807-16852807 - 587256 COSM219021 c.908G>A p.R303H Substitution - Missense 23:16852606-16852606 - GC_350T-GC_350N COSM4772070 c.416T>C p.I139T Substitution - Missense 23:16858741-16858741 - TCGA-DC-5337-01 COSM300111 c.1019G>A p.R340H Substitution - Missense 23:16852067-16852067 - Gp5D COSM300111 c.1019G>A p.R340H Substitution - Missense 23:16852067-16852067 - CSCC-31-T COSM4544941 c.234G>C p.L78L Substitution - coding silent 23:16863028-16863028 - HCC6 COSM1625748 c.842A>G p.N281S Substitution - Missense 23:16852792-16852792 - T44 COSM5345963 c.597+10G>A p.? Unknown 23:16857584-16857584 - TCGA-IR-A3LA-01 COSM4844483 c.949G>A p.D317N Substitution - Missense 23:16852565-16852565 - TCGA-AO-A1KS-01 COSM1490740 c.715G>C p.E239Q Substitution - Missense 23:16853725-16853725 - LAU50_1 COSM233236 c.592G>A p.D198N Substitution - Missense 23:16857599-16857599 - BRC7 COSM5028854 c.1012G>A p.D338N Substitution - Missense 23:16852074-16852074 - TCGA-AX-A0J0-01 COSM1118566 c.634G>T p.E212* Substitution - Nonsense 23:16853806-16853806 - TCGA-AA-A00N-01 COSM277022 c.820G>A p.E274K Substitution - Missense 23:16852814-16852814 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.495755 Xp22.2 300825

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.L280P c.839T>C X 16871856 UCEC C A Missense p.S87I c.260G>T X 16887232 HNSC C A Missense p.V341L c.1021G>T X 16870748 OV C A SpliceAcceptorSNV . c.440-1G>T X 16876973 SCLC C A SpliceDonorSNV . c.1341+1G>T X 16863950 BRCA C G Missense p.D117H c.349G>C X 16881168 HNSC C G Missense p.E283Q c.847G>C X 16871848 BRCA C G Missense p.E438Q c.1312G>C X 16863980 HNSC C G Missense p.W85C c.255G>C X 16887237 HNSC C T Missense p.D382N c.1144G>A X 16870197 BRCA C T Missense p.R172H c.515G>A X 16876897 STAD C T Missense p.R347H c.1040G>A X 16870729 PAAD G A IntronicSNV . c.149-10C>T X 16887353 NSCLC G A Missense p.H219Y c.655C>T X 16875791 STAD G A Missense p.H359Y c.1075C>T X 16870694 CM G A Missense p.R172C c.514C>T X 16876898 STAD G A Missense p.T460M c.1379C>T X 16863189 COREAD G A Synonymous p.F356F c.1068C>T X 16870701 OV G A Synonymous p.L122L c.364C>T X 16881153 LUSC G A Synonymous p.N251N c.753C>T X 16871942 UCEC G A Synonymous p.S306S c.918C>T X 16870971 CM G C Missense p.H243D c.727C>G X 16875719 CM G - Frameshift p.H354Ifs*32 c.1060delC X 16870709 LUAD G T Missense p.P72Q c.215C>A X 16887277 STAD T A IntronicSNV . c.890+46A>T X 16871759 NSCLC T A Missense p.H413L c.1238A>T X 16864054 BLCA T C IntronicSNV . c.1230+862A>G X 16866505 MB T C Missense p.Y224C c.671A>G X 16875775 UCEC T G Missense p.N320H c.958A>C X 16870931 STAD T G Missense p.N386T c.1157A>C X 16870184 HNSC