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 22 20457929 20457929 + Missense_Mutation SNP C C T TCGA-C4-A0F1-01A-11D-A10S-08 TCGA-C4-A0F1-10A-01D-A10S-08 g.chr22:20457929C>T c.3373G>A c.(3373-3375)Ggt>Agt p.G1125S BLCA 22 20458035 20458035 + Silent SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr22:20458035C>T c.3267G>A c.(3265-3267)ccG>ccA p.P1089P BLCA 22 20458068 20458068 + Silent SNP G G A TCGA-FD-A3B3-01A-12D-A202-08 TCGA-FD-A3B3-10A-01D-A202-08 g.chr22:20458068G>A c.3234C>T c.(3232-3234)ttC>ttT p.F1078F BLCA 22 20458116 20458116 + Silent SNP C C G TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr22:20458116C>G c.3186G>C c.(3184-3186)cgG>cgC p.R1062R BLCA 22 20458133 20458133 + Missense_Mutation SNP C C T TCGA-ZF-A9RG-01A-21D-A42E-08 TCGA-ZF-A9RG-10A-01D-A42H-08 g.chr22:20458133C>T c.3169G>A c.(3169-3171)Gag>Aag p.E1057K BLCA 22 20458674 20458674 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr22:20458674G>T c.2628C>A c.(2626-2628)ttC>ttA p.F876L BRCA 22 20456765 20456765 + Missense_Mutation SNP G G A TCGA-AC-A23G-01A-11D-A20S-09 TCGA-AC-A23G-11A-12D-A20S-09 g.chr22:20456765G>A c.4537C>T c.(4537-4539)Cgc>Tgc p.R1513C BRCA 22 20456978 20456978 + Missense_Mutation SNP C C T TCGA-B6-A0WZ-01A-11D-A10G-09 TCGA-B6-A0WZ-10A-01D-A10G-09 g.chr22:20456978C>T c.4324G>A c.(4324-4326)Ggc>Agc p.G1442S BRCA 22 20457060 20457060 + Silent SNP C C G TCGA-A8-A07J-01A-11W-A019-09 TCGA-A8-A07J-10A-01W-A021-09 g.chr22:20457060C>G c.4242G>C c.(4240-4242)gtG>gtC p.V1414V BRCA 22 20458076 20458076 + Missense_Mutation SNP C C T TCGA-AR-A2LR-01A-12D-A18P-09 TCGA-AR-A2LR-10A-01D-A18P-09 g.chr22:20458076C>T c.3226G>A c.(3226-3228)Gtc>Atc p.V1076I CESC 22 20457501 20457501 + Silent SNP C C T TCGA-FU-A5XV-01A-11D-A28B-09 TCGA-FU-A5XV-10A-01D-A28E-09 g.chr22:20457501C>T c.3801G>A c.(3799-3801)ccG>ccA p.P1267P CESC 22 20457737 20457737 + Missense_Mutation SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr22:20457737G>A c.3565C>T c.(3565-3567)Cac>Tac p.H1189Y CESC 22 20457822 20457822 + Silent SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr22:20457822C>T c.3480G>A c.(3478-3480)caG>caA p.Q1160Q CHOL 22 20458094 20458094 + Missense_Mutation SNP C C G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr22:20458094C>G c.3208G>C c.(3208-3210)Gga>Cga p.G1070R COAD 22 20456536 20456536 + Frame_Shift_Del DEL C C - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr22:20456536delC c.4766delG c.(4765-4767)ggcfs p.G1589fs COAD 22 20457098 20457098 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:20457098G>A c.4204C>T c.(4204-4206)Cct>Tct p.P1402S COAD 22 20458127 20458127 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr22:20458127G>A c.3175C>T c.(3175-3177)Cgg>Tgg p.R1059W COAD 22 20459342 20459343 + Frame_Shift_Ins INS - - GG TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr22:20459342_20459343insGG c.1959_1960insCC c.(1957-1962)tccggcfs p.G654fs COAD 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del COAD 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del COAD 22 20460135 20460135 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr22:20460135G>A c.1167C>T c.(1165-1167)cgC>cgT p.R389R COADREAD 22 20456536 20456536 + Frame_Shift_Del DEL C C - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr22:20456536delC c.4766delG c.(4765-4767)ggcfs p.G1589fs COADREAD 22 20457098 20457098 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:20457098G>A c.4204C>T c.(4204-4206)Cct>Tct p.P1402S COADREAD 22 20458127 20458127 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr22:20458127G>A c.3175C>T c.(3175-3177)Cgg>Tgg p.R1059W COADREAD 22 20459342 20459343 + Frame_Shift_Ins INS - - GG TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr22:20459342_20459343insGG c.1959_1960insCC c.(1957-1962)tccggcfs p.G654fs COADREAD 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del COADREAD 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del COADREAD 22 20460135 20460135 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr22:20460135G>A c.1167C>T c.(1165-1167)cgC>cgT p.R389R ESCA 22 20456704 20456704 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr22:20456704G>A c.4598C>T c.(4597-4599)gCc>gTc p.A1533V GBM 22 20458153 20458153 + Missense_Mutation SNP G G A TCGA-41-3392-01A-01D-1495-08 TCGA-41-3392-10A-01D-1495-08 g.chr22:20458153G>A c.3149C>T c.(3148-3150)aCg>aTg p.T1050M GBM 22 20458191 20458191 + Silent SNP G G A TCGA-12-0619-01A-01D-1492-08 TCGA-12-0619-10A-01D-1492-08 g.chr22:20458191G>A c.3111C>T c.(3109-3111)ggC>ggT p.G1037G GBM 22 20458331 20458331 + Missense_Mutation SNP C C G TCGA-19-2625-01A-01D-1495-08 TCGA-19-2625-10A-01D-1495-08 g.chr22:20458331C>G c.2971G>C c.(2971-2973)Gtg>Ctg p.V991L GBMLGG 22 20458153 20458153 + Missense_Mutation SNP G G A TCGA-41-3392-01A-01D-1495-08 TCGA-41-3392-10A-01D-1495-08 g.chr22:20458153G>A c.3149C>T c.(3148-3150)aCg>aTg p.T1050M GBMLGG 22 20458191 20458191 + Silent SNP G G A TCGA-12-0619-01A-01D-1492-08 TCGA-12-0619-10A-01D-1492-08 g.chr22:20458191G>A c.3111C>T c.(3109-3111)ggC>ggT p.G1037G GBMLGG 22 20458331 20458331 + Missense_Mutation SNP C C G TCGA-19-2625-01A-01D-1495-08 TCGA-19-2625-10A-01D-1495-08 g.chr22:20458331C>G c.2971G>C c.(2971-2973)Gtg>Ctg p.V991L HNSC 22 20457160 20457160 + Missense_Mutation SNP T T A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr22:20457160T>A c.4142A>T c.(4141-4143)gAg>gTg p.E1381V HNSC 22 20457162 20457162 + Silent SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr22:20457162C>T c.4140G>A c.(4138-4140)aaG>aaA p.K1380K HNSC 22 20457913 20457913 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr22:20457913G>A c.3389C>T c.(3388-3390)gCa>gTa p.A1130V HNSC 22 20458180 20458180 + Missense_Mutation SNP T T A TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr22:20458180T>A c.3122A>T c.(3121-3123)tAc>tTc p.Y1041F HNSC 22 20458538 20458538 + Nonsense_Mutation SNP G G A TCGA-CR-6467-01A-11D-1870-08 TCGA-CR-6467-10A-01D-1870-08 g.chr22:20458538G>A c.2764C>T c.(2764-2766)Cag>Tag p.Q922* HNSC 22 20458649 20458649 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr22:20458649G>A c.2653C>T c.(2653-2655)Cgg>Tgg p.R885W HNSC 22 20460094 20460094 + Missense_Mutation SNP C C G TCGA-QK-A6VC-01A-23D-A34J-08 TCGA-QK-A6VC-10B-01D-A34M-08 g.chr22:20460094C>G c.1208G>C c.(1207-1209)cGt>cCt p.R403P HNSC 22 20460137 20460137 + Missense_Mutation SNP G G T TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr22:20460137G>T c.1165C>A c.(1165-1167)Cgc>Agc p.R389S KICH 22 20458628 20458629 + Frame_Shift_Ins INS - - G TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chr22:20458628_20458629insG c.2673_2674insC c.(2671-2676)tccaacfs p.N892fs KICH 22 20458634 20458635 + Frame_Shift_Ins INS - - C TCGA-KO-8409-01A-11D-2310-10 TCGA-KO-8409-11A-01D-2311-10 g.chr22:20458634_20458635insC c.2667_2668insG c.(2665-2670)gtgcccfs p.P890fs KIPAN 22 20458121 20458122 + Frame_Shift_Ins INS - - C TCGA-B0-4945-01A-01D-1421-08 TCGA-B0-4945-11A-01D-1421-08 g.chr22:20458121_20458122insC c.3180_3181insG c.(3178-3183)ctgccafs p.P1061fs KIPAN 22 20458628 20458629 + Frame_Shift_Ins INS - - G TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chr22:20458628_20458629insG c.2673_2674insC c.(2671-2676)tccaacfs p.N892fs KIPAN 22 20458634 20458635 + Frame_Shift_Ins INS - - C TCGA-KO-8409-01A-11D-2310-10 TCGA-KO-8409-11A-01D-2311-10 g.chr22:20458634_20458635insC c.2667_2668insG c.(2665-2670)gtgcccfs p.P890fs KIPAN 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-BP-4164-01A-02D-1386-10 TCGA-BP-4164-11A-01D-1251-10 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del KIPAN 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-BP-4964-01A-01D-1462-08 TCGA-BP-4964-11A-01D-1462-08 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del KIRC 22 20458121 20458122 + Frame_Shift_Ins INS - - C TCGA-B0-4945-01A-01D-1421-08 TCGA-B0-4945-11A-01D-1421-08 g.chr22:20458121_20458122insC c.3180_3181insG c.(3178-3183)ctgccafs p.P1061fs KIRC 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-BP-4164-01A-02D-1386-10 TCGA-BP-4164-11A-01D-1251-10 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del KIRC 22 20460113 20460115 + In_Frame_Del DEL CCG CCG - TCGA-BP-4964-01A-01D-1462-08 TCGA-BP-4964-11A-01D-1462-08 g.chr22:20460113_20460115delCCG c.1187_1189delCGG c.(1186-1191)gcggag>gag p.A396del LIHC 22 20457887 20457887 + Missense_Mutation SNP C C A TCGA-DD-AAW0-01A-11D-A40R-10 TCGA-DD-AAW0-10A-01D-A40U-10 g.chr22:20457887C>A c.3415G>T c.(3415-3417)Gcc>Tcc p.A1139S LIHC 22 20458090 20458090 + Missense_Mutation SNP G G T TCGA-RC-A6M6-01A-11D-A32G-10 TCGA-RC-A6M6-10A-01D-A32G-10 g.chr22:20458090G>T c.3212C>A c.(3211-3213)aCt>aAt p.T1071N LIHC 22 20458139 20458139 + Missense_Mutation SNP G G A TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr22:20458139G>A c.3163C>T c.(3163-3165)Cgg>Tgg p.R1055W LUAD 22 20457080 20457080 + Missense_Mutation SNP G G T TCGA-62-8399-01A-21D-2323-08 TCGA-62-8399-10A-01D-2323-08 g.chr22:20457080G>T c.4222C>A c.(4222-4224)Caa>Aaa p.Q1408K LUAD 22 20457848 20457848 + Frame_Shift_Del DEL G G - TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr22:20457848delG c.3454delC c.(3454-3456)cagfs p.Q1152fs LUAD 22 20458191 20458191 + Silent SNP G G T TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr22:20458191G>T c.3111C>A c.(3109-3111)ggC>ggA p.G1037G LUSC 22 20457269 20457269 + Missense_Mutation SNP C C A TCGA-60-2723-01A-01D-1522-08 TCGA-60-2723-11A-01D-1522-08 g.chr22:20457269C>A c.4033G>T c.(4033-4035)Gct>Tct p.A1345S OV 22 20458524 20458524 + Silent SNP C C A TCGA-09-1675-01B-01W-0633-09 TCGA-09-1675-10A-01W-0633-09 g.chr22:20458524C>A c.2778G>T c.(2776-2778)ctG>ctT p.L926L PAAD 22 20457064 20457064 + Missense_Mutation SNP C C T TCGA-XD-AAUL-01A-21D-A397-08 TCGA-XD-AAUL-10A-01D-A39A-08 g.chr22:20457064C>T c.4238G>A c.(4237-4239)gGg>gAg p.G1413E PAAD 22 20458364 20458364 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr22:20458364C>A c.2938G>T c.(2938-2940)Ggc>Tgc p.G980C PAAD 22 20459530 20459530 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr22:20459530G>A c.1772C>T c.(1771-1773)gCg>gTg p.A591V PRAD 22 20457106 20457106 + Missense_Mutation SNP C C T TCGA-HC-7744-01A-11D-2114-08 TCGA-HC-7744-10A-01D-2115-08 g.chr22:20457106C>T c.4196G>A c.(4195-4197)aGg>aAg p.R1399K PRAD 22 20457165 20457165 + Missense_Mutation SNP C C G TCGA-J4-A83I-01A-11D-A364-08 TCGA-J4-A83I-10B-01D-A362-08 g.chr22:20457165C>G c.4137G>C c.(4135-4137)ttG>ttC p.L1379F PRAD 22 20458475 20458475 + Missense_Mutation SNP C C T TCGA-CH-5754-01A-11D-1576-08 TCGA-CH-5754-10A-01D-1576-08 g.chr22:20458475C>T c.2827G>A c.(2827-2829)Ggg>Agg p.G943R SARC 22 20458271 20458271 + Missense_Mutation SNP T T C TCGA-QQ-A5VC-01A-31D-A32I-09 TCGA-QQ-A5VC-10A-01D-A32I-09 g.chr22:20458271T>C c.3031A>G c.(3031-3033)Atc>Gtc p.I1011V SARC 22 20458608 20458608 + Silent SNP C C A TCGA-IE-A4EI-01A-11D-A24N-09 TCGA-IE-A4EI-10A-01D-A24N-09 g.chr22:20458608C>A c.2694G>T c.(2692-2694)ccG>ccT p.P898P SKCM 22 20457137 20457137 + Missense_Mutation SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr22:20457137C>T c.4165G>A c.(4165-4167)Gat>Aat p.D1389N SKCM 22 20457175 20457175 + Missense_Mutation SNP T T A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr22:20457175T>A c.4127A>T c.(4126-4128)cAt>cTt p.H1376L SKCM 22 20457900 20457900 + Silent SNP C C T TCGA-GN-A268-06A-11D-A196-08 TCGA-GN-A268-10A-01D-A198-08 g.chr22:20457900C>T c.3402G>A c.(3400-3402)aaG>aaA p.K1134K SKCM 22 20457978 20457978 + Silent SNP G G A TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr22:20457978G>A c.3324C>T c.(3322-3324)ctC>ctT p.L1108L SKCM 22 20458067 20458067 + Missense_Mutation SNP C C A TCGA-D3-A3C3-06A-12D-A19A-08 TCGA-D3-A3C3-10A-01D-A19A-08 g.chr22:20458067C>A c.3235G>T c.(3235-3237)Gac>Tac p.D1079Y SKCM 22 20458068 20458068 + Silent SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr22:20458068G>A c.3234C>T c.(3232-3234)ttC>ttT p.F1078F SKCM 22 20458068 20458068 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr22:20458068G>A c.3234C>T c.(3232-3234)ttC>ttT p.F1078F SKCM 22 20458093 20458093 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr22:20458093C>T c.3209G>A c.(3208-3210)gGa>gAa p.G1070E SKCM 22 20458239 20458239 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr22:20458239G>A c.3063C>T c.(3061-3063)ccC>ccT p.P1021P SKCM 22 20458247 20458247 + Missense_Mutation SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr22:20458247G>A c.3055C>T c.(3055-3057)Cgc>Tgc p.R1019C SKCM 22 20458667 20458667 + Missense_Mutation SNP C C T TCGA-EE-A2MP-06A-11D-A197-08 TCGA-EE-A2MP-10A-01D-A199-08 g.chr22:20458667C>T c.2635G>A c.(2635-2637)Ggg>Agg p.G879R SKCM 22 20458668 20458668 + Silent SNP C C T TCGA-EE-A2MP-06A-11D-A197-08 TCGA-EE-A2MP-10A-01D-A199-08 g.chr22:20458668C>T c.2634G>A c.(2632-2634)gaG>gaA p.E878E

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.115429 22q11.21 612699

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - A Frameshift p.G1144Wfs*29 c.3429dupT 22 20457873 PAAD C A Missense p.A1345S c.4033G>T 22 20457269 LUSC C A Missense p.C1170F c.3509G>T 22 20457793 THCA C A Missense p.D1079Y c.3235G>T 22 20458067 CM CCG - InFrameDeletion p.A396delA c.1187_1189delCGG 22 20460113 RCCC CC TT Missense p.G879R c.2634_2635delinsAA 22 20458667 CM - C Frameshift p.P1061Afs*53 c.3180dupG 22 20458122 RCCC C G Missense p.V991L c.2971G>C 22 20458331 GBM C G Synonymous p.L1093L c.3279G>C 22 20458023 BRCA C T Missense p.A1367T c.4099G>A 22 20457203 LGG C T Missense p.D1389N c.4165G>A 22 20457137 CM C T Missense p.G1125S c.3373G>A 22 20457929 BLCA C T Missense p.G1442S c.4324G>A 22 20456978 BRCA C T Missense p.G943R c.2827G>A 22 20458475 PRAD C T Missense p.R1399K c.4196G>A 22 20457106 PRAD C T Synonymous p.K1134K c.3402G>A 22 20457900 CM G A Missense p.A1036V c.3107C>T 22 20458195 UCEC G A Missense p.A920V c.2759C>T 22 20458543 BRCA G A Missense p.P1086L c.3257C>T 22 20458045 UCEC G A Missense p.R1019C c.3055C>T 22 20458247 CM G A Missense p.T1042I c.3125C>T 22 20458177 CM G A Missense p.T1050M c.3149C>T 22 20458153 GBM G A Nonsense p.Q1364* c.4090C>T 22 20457212 CM G A Nonsense p.Q922* c.2764C>T 22 20458538 HNSC G A Synonymous p.F1078F c.3234C>T 22 20458068 BLCA G A Synonymous p.F1078F c.3234C>T 22 20458068 CM G A Synonymous p.F893F c.2679C>T 22 20458623 CM G A Synonymous p.G1037G c.3111C>T 22 20458191 GBM G A Synonymous p.L1108L c.3324C>T 22 20457978 CM G A Synonymous p.P996P c.2988C>T 22 20458314 LGG G A Synonymous p.S1432S c.4296C>T 22 20457006 THCA G T Missense p.Q998K c.2992C>A 22 20458310 UCEC T A Missense p.Y1041F c.3122A>T 22 20458180 HNSC T G Missense p.E1263A c.3788A>C 22 20457514 COREAD