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 9 110062443 110062451 + In_Frame_Del DEL ATTGAATCT ATTGAATCT - TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr9:110062443_110062451delATTGAATCT c.88_96delATTGAATCT c.(88-96)attgaatctdel p.IES30del BLCA 9 110081037 110081037 + Silent SNP G G T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr9:110081037G>T c.558G>T c.(556-558)acG>acT p.T186T BLCA 9 110086241 110086241 + Silent SNP T T C TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr9:110086241T>C c.888T>C c.(886-888)ccT>ccC p.P296P BLCA 9 110086268 110086268 + Missense_Mutation SNP G G C TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr9:110086268G>C c.915G>C c.(913-915)caG>caC p.Q305H BLCA 9 110091908 110091908 + Missense_Mutation SNP C C T TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr9:110091908C>T c.1201C>T c.(1201-1203)Ctt>Ttt p.L401F BRCA 9 110068789 110068789 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr9:110068789A>C c.358A>C c.(358-360)Act>Cct p.T120P BRCA 9 110081065 110081065 + Missense_Mutation SNP G G A TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr9:110081065G>A c.586G>A c.(586-588)Gag>Aag p.E196K BRCA 9 110086219 110086219 + Missense_Mutation SNP G G A TCGA-BH-A0WA-01A-11D-A10G-09 TCGA-BH-A0WA-10A-01D-A117-09 g.chr9:110086219G>A c.866G>A c.(865-867)aGa>aAa p.R289K BRCA 9 110086287 110086287 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr9:110086287C>G c.934C>G c.(934-936)Caa>Gaa p.Q312E BRCA 9 110091887 110091887 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr9:110091887G>A c.1180G>A c.(1180-1182)Gag>Aag p.E394K CESC 9 110068756 110068756 + Nonsense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr9:110068756C>T c.325C>T c.(325-327)Cag>Tag p.Q109* CESC 9 110068879 110068879 + Missense_Mutation SNP G G A TCGA-C5-A1BL-01A-11D-A13W-08 TCGA-C5-A1BL-10A-01D-A13W-08 g.chr9:110068879G>A c.448G>A c.(448-450)Gaa>Aaa p.E150K CESC 9 110086276 110086276 + Missense_Mutation SNP G G A TCGA-MU-A51Y-01A-11D-A26G-09 TCGA-MU-A51Y-10A-01D-A26G-09 g.chr9:110086276G>A c.923G>A c.(922-924)cGa>cAa p.R308Q CESC 9 110087185 110087185 + Missense_Mutation SNP G G C TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr9:110087185G>C c.1016G>C c.(1015-1017)gGa>gCa p.G339A COAD 9 110068775 110068775 + Missense_Mutation SNP C C A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr9:110068775C>A c.344C>A c.(343-345)cCt>cAt p.P115H COAD 9 110081036 110081036 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:110081036C>T c.557C>T c.(556-558)aCg>aTg p.T186M COAD 9 110081108 110081108 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:110081108C>T c.629C>T c.(628-630)gCc>gTc p.A210V COAD 9 110091864 110091864 + Missense_Mutation SNP C C T TCGA-AA-3684-01A-02W-0900-09 TCGA-AA-3684-10A-01W-0900-09 g.chr9:110091864C>T c.1157C>T c.(1156-1158)gCg>gTg p.A386V COADREAD 9 110068775 110068775 + Missense_Mutation SNP C C A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr9:110068775C>A c.344C>A c.(343-345)cCt>cAt p.P115H COADREAD 9 110081036 110081036 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:110081036C>T c.557C>T c.(556-558)aCg>aTg p.T186M COADREAD 9 110081108 110081108 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:110081108C>T c.629C>T c.(628-630)gCc>gTc p.A210V COADREAD 9 110091864 110091864 + Missense_Mutation SNP C C T TCGA-AA-3684-01A-02W-0900-09 TCGA-AA-3684-10A-01W-0900-09 g.chr9:110091864C>T c.1157C>T c.(1156-1158)gCg>gTg p.A386V GBM 9 110084309 110084309 + Nonsense_Mutation SNP C C T TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr9:110084309C>T c.727C>T c.(727-729)Caa>Taa p.Q243* GBM 9 110084381 110084383 + In_Frame_Del DEL ACA ACA - TCGA-27-2519-01A-01D-1494-08 TCGA-27-2519-10A-01D-1494-08 g.chr9:110084381_110084383delACA c.799_801delACA c.(799-801)acadel p.T269del GBMLGG 9 110084309 110084309 + Nonsense_Mutation SNP C C T TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr9:110084309C>T c.727C>T c.(727-729)Caa>Taa p.Q243* GBMLGG 9 110084381 110084383 + In_Frame_Del DEL ACA ACA - TCGA-27-2519-01A-01D-1494-08 TCGA-27-2519-10A-01D-1494-08 g.chr9:110084381_110084383delACA c.799_801delACA c.(799-801)acadel p.T269del GBMLGG 9 110086280 110086280 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:110086280G>T c.927G>T c.(925-927)gaG>gaT p.E309D HNSC 9 110073972 110073972 + Silent SNP T T C TCGA-CN-6994-01A-11D-1912-08 TCGA-CN-6994-10A-01D-1912-08 g.chr9:110073972T>C c.507T>C c.(505-507)ggT>ggC p.G169G HNSC 9 110086243 110086243 + Missense_Mutation SNP C C T TCGA-BA-4078-01A-01D-1434-08 TCGA-BA-4078-10A-01D-1434-08 g.chr9:110086243C>T c.890C>T c.(889-891)tCc>tTc p.S297F HNSC 9 110087223 110087223 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr9:110087223G>A c.1054G>A c.(1054-1056)Gct>Act p.A352T HNSC 9 110091856 110091856 + Silent SNP G G C TCGA-BA-A6DJ-01A-11D-A30E-08 TCGA-BA-A6DJ-10A-01D-A30H-08 g.chr9:110091856G>C c.1149G>C c.(1147-1149)gtG>gtC p.V383V KICH 9 110068852 110068852 + Missense_Mutation SNP A A T TCGA-KN-8432-01A-11D-2310-10 TCGA-KN-8432-11A-01D-2311-10 g.chr9:110068852A>T c.421A>T c.(421-423)Agt>Tgt p.S141C KIPAN 9 110068852 110068852 + Missense_Mutation SNP A A T TCGA-KN-8432-01A-11D-2310-10 TCGA-KN-8432-11A-01D-2311-10 g.chr9:110068852A>T c.421A>T c.(421-423)Agt>Tgt p.S141C KIPAN 9 110084347 110084348 + Frame_Shift_Del DEL GG GG - TCGA-CZ-4862-01A-01D-1373-10 TCGA-CZ-4862-11A-01D-1373-10 g.chr9:110084347_110084348delGG c.765_766delGG c.(763-768)gtggctfs p.A260fs KIPAN 9 110091836 110091836 + Missense_Mutation SNP G G A TCGA-GL-8500-01A-11D-2396-08 TCGA-GL-8500-10A-01D-2396-08 g.chr9:110091836G>A c.1129G>A c.(1129-1131)Gga>Aga p.G377R KIRC 9 110084347 110084348 + Frame_Shift_Del DEL GG GG - TCGA-CZ-4862-01A-01D-1373-10 TCGA-CZ-4862-11A-01D-1373-10 g.chr9:110084347_110084348delGG c.765_766delGG c.(763-768)gtggctfs p.A260fs KIRP 9 110091836 110091836 + Missense_Mutation SNP G G A TCGA-GL-8500-01A-11D-2396-08 TCGA-GL-8500-10A-01D-2396-08 g.chr9:110091836G>A c.1129G>A c.(1129-1131)Gga>Aga p.G377R LGG 9 110086280 110086280 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:110086280G>T c.927G>T c.(925-927)gaG>gaT p.E309D LIHC 9 110045933 110045933 + Missense_Mutation SNP T T C TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr9:110045933T>C c.23T>C c.(22-24)cTc>cCc p.L8P LIHC 9 110064350 110064350 + Silent SNP A A G TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr9:110064350A>G c.183A>G c.(181-183)gaA>gaG p.E61E LIHC 9 110081131 110081131 + Missense_Mutation SNP C C G TCGA-DD-AACK-01A-11D-A40R-10 TCGA-DD-AACK-10A-01D-A40U-10 g.chr9:110081131C>G c.652C>G c.(652-654)Cct>Gct p.P218A LIHC 9 110091920 110091920 + Missense_Mutation SNP A A G TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr9:110091920A>G c.1213A>G c.(1213-1215)Aac>Gac p.N405D LIHC 9 110091936 110091936 + Nonstop_Mutation SNP G G T TCGA-BC-A8YO-01A-11D-A36X-10 TCGA-BC-A8YO-10A-01D-A370-10 g.chr9:110091936G>T c.1229G>T c.(1228-1230)tGa>tTa p.*410L LUAD 9 110068802 110068802 + Missense_Mutation SNP C C A TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr9:110068802C>A c.371C>A c.(370-372)gCa>gAa p.A124E LUAD 9 110074006 110074006 + Missense_Mutation SNP A A G TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr9:110074006A>G c.541A>G c.(541-543)Acg>Gcg p.T181A LUAD 9 110084315 110084315 + Missense_Mutation SNP G G T TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr9:110084315G>T c.733G>T c.(733-735)Gct>Tct p.A245S LUAD 9 110087176 110087176 + Missense_Mutation SNP G G T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr9:110087176G>T c.1007G>T c.(1006-1008)gGt>gTt p.G336V LUAD 9 110087285 110087285 + Splice_Site SNP G G T TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr9:110087285G>T c.1116G>T c.(1114-1116)agG>agT p.R372S OV 9 110081063 110081063 + Missense_Mutation SNP C C T TCGA-13-1411-01A-01W-0494-09 TCGA-13-1411-10A-01W-0495-09 g.chr9:110081063C>T c.584C>T c.(583-585)aCt>aTt p.T195I PAAD 9 110084292 110084292 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:110084292C>T c.710C>T c.(709-711)gCt>gTt p.A237V PAAD 9 110087200 110087200 + Missense_Mutation SNP G G C TCGA-2L-AAQM-01A-11D-A397-08 TCGA-2L-AAQM-11A-11D-A39A-08 g.chr9:110087200G>C c.1031G>C c.(1030-1032)gGt>gCt p.G344A SKCM 9 110081045 110081045 + Missense_Mutation SNP C C A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:110081045C>A c.566C>A c.(565-567)tCt>tAt p.S189Y SKCM 9 110081063 110081063 + Missense_Mutation SNP C C A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr9:110081063C>A c.584C>A c.(583-585)aCt>aAt p.T195N SKCM 9 110086177 110086177 + Missense_Mutation SNP C C T TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr9:110086177C>T c.824C>T c.(823-825)cCc>cTc p.P275L SKCM 9 110086240 110086240 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:110086240C>T c.887C>T c.(886-888)cCt>cTt p.P296L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 9 110062443 110062451 deletion of <=200bp ATTGAATCT - 5_prime_UTR_variant BLCA-US 9 110062443 110062451 deletion of <=200bp ATTGAATCT - inframe_deletion IES30 BLCA-US 9 110062443 110062451 deletion of <=200bp ATTGAATCT - inframe_deletion IES9 BLCA-US 9 110086268 110086268 single base substitution G C intron_variant BLCA-US 9 110086268 110086268 single base substitution G C missense_variant Q233H 699G>C BLCA-US 9 110086268 110086268 single base substitution G C missense_variant Q305H 915G>C BRCA-EU 9 110040773 110040773 single base substitution A C upstream_gene_variant BRCA-EU 9 110040840 110040840 insertion of <=200bp - A upstream_gene_variant BRCA-EU 9 110040921 110040921 single base substitution A G upstream_gene_variant BRCA-EU 9 110042063 110042063 insertion of <=200bp - A upstream_gene_variant BRCA-EU 9 110042922 110042922 single base substitution G C upstream_gene_variant BRCA-EU 9 110043277 110043277 single base substitution A C upstream_gene_variant BRCA-EU 9 110043657 110043657 single base substitution G C upstream_gene_variant BRCA-EU 9 110045109 110045109 single base substitution G T upstream_gene_variant BRCA-EU 9 110045113 110045113 single base substitution C T upstream_gene_variant BRCA-EU 9 110045223 110045223 single base substitution C G upstream_gene_variant BRCA-EU 9 110045556 110045556 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 9 110045556 110045556 single base substitution C G upstream_gene_variant BRCA-EU 9 110046388 110046388 single base substitution C G 5_prime_UTR_variant BRCA-EU 9 110046388 110046388 single base substitution C G intron_variant BRCA-EU 9 110046388 110046388 single base substitution C G upstream_gene_variant BRCA-EU 9 110048298 110048298 single base substitution G A intron_variant BRCA-EU 9 110048648 110048648 single base substitution C G intron_variant BRCA-EU 9 110049656 110049656 single base substitution G T intron_variant BRCA-EU 9 110051639 110051639 deletion of <=200bp T - intron_variant BRCA-EU 9 110052623 110052623 single base substitution T C intron_variant BRCA-EU 9 110053176 110053176 single base substitution C T intron_variant BRCA-EU 9 110053865 110053865 single base substitution T A intron_variant BRCA-EU 9 110054020 110054020 single base substitution A C intron_variant BRCA-EU 9 110054527 110054527 single base substitution G T intron_variant BRCA-EU 9 110056572 110056572 single base substitution C T intron_variant BRCA-EU 9 110057191 110057191 single base substitution A G intron_variant BRCA-EU 9 110057820 110057820 single base substitution C A intron_variant BRCA-EU 9 110058201 110058201 single base substitution A T intron_variant BRCA-EU 9 110059669 110059669 single base substitution G A intron_variant BRCA-EU 9 110059976 110059976 single base substitution T G intron_variant BRCA-EU 9 110061131 110061131 single base substitution A T intron_variant BRCA-EU 9 110061492 110061492 single base substitution T A intron_variant BRCA-EU 9 110062798 110062798 single base substitution A G intron_variant BRCA-EU 9 110062926 110062926 single base substitution T A intron_variant BRCA-EU 9 110063124 110063124 single base substitution G C intron_variant BRCA-EU 9 110064978 110064978 single base substitution C A intron_variant BRCA-EU 9 110064978 110064978 single base substitution C A upstream_gene_variant BRCA-EU 9 110065632 110065632 single base substitution T A intron_variant BRCA-EU 9 110065632 110065632 single base substitution T A upstream_gene_variant BRCA-EU 9 110065693 110065693 single base substitution G A intron_variant BRCA-EU 9 110065693 110065693 single base substitution G A upstream_gene_variant BRCA-EU 9 110067082 110067082 single base substitution A G intron_variant BRCA-EU 9 110067082 110067082 single base substitution A G upstream_gene_variant BRCA-EU 9 110068139 110068139 single base substitution C G intron_variant BRCA-EU 9 110068139 110068139 single base substitution C G upstream_gene_variant BRCA-EU 9 110069504 110069504 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 110069504 110069504 deletion of <=200bp A - intron_variant BRCA-EU 9 110072153 110072153 single base substitution A C downstream_gene_variant BRCA-EU 9 110072153 110072153 single base substitution A C intron_variant BRCA-EU 9 110073595 110073595 single base substitution C T downstream_gene_variant BRCA-EU 9 110073595 110073595 single base substitution C T intron_variant BRCA-EU 9 110074457 110074457 single base substitution A G intron_variant BRCA-EU 9 110076582 110076582 single base substitution A G intron_variant BRCA-EU 9 110077223 110077223 single base substitution G C intron_variant BRCA-EU 9 110077386 110077386 single base substitution C T intron_variant BRCA-EU 9 110078458 110078458 deletion of <=200bp T - intron_variant BRCA-EU 9 110078988 110078988 single base substitution T A intron_variant BRCA-EU 9 110079120 110079120 single base substitution A G intron_variant BRCA-EU 9 110079452 110079453 deletion of <=200bp AA - intron_variant BRCA-EU 9 110079913 110079913 single base substitution A G intron_variant BRCA-EU 9 110079937 110079937 single base substitution G T intron_variant BRCA-EU 9 110080263 110080263 single base substitution G C intron_variant BRCA-EU 9 110080750 110080750 single base substitution A G intron_variant BRCA-EU 9 110081004 110081004 deletion of <=200bp T - intron_variant BRCA-EU 9 110081573 110081573 single base substitution G A intron_variant BRCA-EU 9 110082037 110082037 deletion of <=200bp T - intron_variant BRCA-EU 9 110084279 110084282 deletion of <=200bp AGAG - frameshift_variant RE161 BRCA-EU 9 110084279 110084282 deletion of <=200bp AGAG - frameshift_variant RE233 BRCA-EU 9 110084279 110084282 deletion of <=200bp AGAG - intron_variant BRCA-EU 9 110084707 110084707 single base substitution G C intron_variant BRCA-EU 9 110085591 110085591 single base substitution T C intron_variant BRCA-EU 9 110085674 110085674 single base substitution C G intron_variant BRCA-EU 9 110086858 110086858 single base substitution G T intron_variant BRCA-EU 9 110087163 110087163 single base substitution G A intron_variant BRCA-EU 9 110087163 110087163 single base substitution G A missense_variant V260I 778G>A BRCA-EU 9 110087163 110087163 single base substitution G A missense_variant V332I 994G>A BRCA-EU 9 110088809 110088809 single base substitution T C intron_variant BRCA-EU 9 110090157 110090157 single base substitution T C intron_variant BRCA-EU 9 110091317 110091317 single base substitution G C intron_variant BRCA-EU 9 110094393 110094393 single base substitution G T 3_prime_UTR_variant BRCA-EU 9 110094393 110094393 single base substitution G T downstream_gene_variant BRCA-EU 9 110094608 110094608 single base substitution G C downstream_gene_variant BRCA-EU 9 110095465 110095465 single base substitution C T downstream_gene_variant BRCA-EU 9 110097987 110097987 single base substitution A G downstream_gene_variant BRCA-EU 9 110099378 110099378 single base substitution T G downstream_gene_variant BRCA-FR 9 110091317 110091317 single base substitution G C intron_variant BRCA-UK 9 110086230 110086230 single base substitution C T intron_variant BRCA-UK 9 110086230 110086230 single base substitution C T stop_gained Q221* 661C>T BRCA-UK 9 110086230 110086230 single base substitution C T stop_gained Q293* 877C>T BRCA-UK 9 110087306 110087306 single base substitution A T intron_variant BRCA-US 9 110068789 110068789 single base substitution A C downstream_gene_variant BRCA-US 9 110068789 110068789 single base substitution A C missense_variant T120P 358A>C BRCA-US 9 110068789 110068789 single base substitution A C missense_variant T48P 142A>C BRCA-US 9 110068789 110068789 single base substitution A C upstream_gene_variant BRCA-US 9 110081065 110081065 single base substitution G A missense_variant E124K 370G>A BRCA-US 9 110081065 110081065 single base substitution G A missense_variant E196K 586G>A BRCA-US 9 110081065 110081065 single base substitution G A missense_variant E65K 193G>A BRCA-US 9 110086219 110086219 single base substitution G A intron_variant BRCA-US 9 110086219 110086219 single base substitution G A missense_variant R217K 650G>A BRCA-US 9 110086219 110086219 single base substitution G A missense_variant R289K 866G>A BRCA-US 9 110086287 110086287 single base substitution C G intron_variant BRCA-US 9 110086287 110086287 single base substitution C G missense_variant Q240E 718C>G BRCA-US 9 110086287 110086287 single base substitution C G missense_variant Q312E 934C>G BRCA-US 9 110091887 110091887 single base substitution G A intron_variant BRCA-US 9 110091887 110091887 single base substitution G A missense_variant E322K 964G>A BRCA-US 9 110091887 110091887 single base substitution G A missense_variant E394K 1180G>A BTCA-JP 9 110064292 110064292 deletion of <=200bp T - intron_variant BTCA-JP 9 110064292 110064292 deletion of <=200bp T - upstream_gene_variant CESC-US 9 110068756 110068756 single base substitution C T downstream_gene_variant CESC-US 9 110068756 110068756 single base substitution C T stop_gained Q109* 325C>T CESC-US 9 110068756 110068756 single base substitution C T stop_gained Q37* 109C>T CESC-US 9 110068756 110068756 single base substitution C T upstream_gene_variant CESC-US 9 110068879 110068879 single base substitution G A downstream_gene_variant CESC-US 9 110068879 110068879 single base substitution G A missense_variant E150K 448G>A CESC-US 9 110068879 110068879 single base substitution G A missense_variant E19K 55G>A CESC-US 9 110068879 110068879 single base substitution G A missense_variant E78K 232G>A CESC-US 9 110086276 110086276 single base substitution G A intron_variant CESC-US 9 110086276 110086276 single base substitution G A missense_variant R236Q 707G>A CESC-US 9 110086276 110086276 single base substitution G A missense_variant R308Q 923G>A CESC-US 9 110087185 110087185 single base substitution G C intron_variant CESC-US 9 110087185 110087185 single base substitution G C missense_variant G267A 800G>C CESC-US 9 110087185 110087185 single base substitution G C missense_variant G339A 1016G>C CLLE-ES 9 110066379 110066400 deletion of <=200bp AGAAATGACCTTATTAATACAA - intron_variant CLLE-ES 9 110066379 110066400 deletion of <=200bp AGAAATGACCTTATTAATACAA - upstream_gene_variant CLLE-ES 9 110093982 110093982 single base substitution A C 3_prime_UTR_variant CLLE-ES 9 110093982 110093982 single base substitution A C downstream_gene_variant CLLE-ES 9 110093982 110093982 single base substitution A C missense_variant K107N 321A>C COAD-US 9 110068775 110068775 single base substitution C A downstream_gene_variant COAD-US 9 110068775 110068775 single base substitution C A missense_variant P115H 344C>A COAD-US 9 110068775 110068775 single base substitution C A missense_variant P43H 128C>A COAD-US 9 110068775 110068775 single base substitution C A upstream_gene_variant COAD-US 9 110084328 110084328 single base substitution C T intron_variant COAD-US 9 110084328 110084328 single base substitution C T missense_variant A177V 530C>T COAD-US 9 110084328 110084328 single base substitution C T missense_variant A249V 746C>T COCA-CN 9 110049914 110049914 single base substitution C G intron_variant COCA-CN 9 110051369 110051369 single base substitution T C intron_variant COCA-CN 9 110059071 110059071 single base substitution C T intron_variant COCA-CN 9 110062143 110062143 single base substitution A T intron_variant COCA-CN 9 110068848 110068848 single base substitution T C downstream_gene_variant COCA-CN 9 110068848 110068848 single base substitution T C synonymous_variant P139P 417T>C COCA-CN 9 110068848 110068848 single base substitution T C synonymous_variant P67P 201T>C COCA-CN 9 110068848 110068848 single base substitution T C synonymous_variant P8P 24T>C COCA-CN 9 110072995 110072995 single base substitution G A downstream_gene_variant COCA-CN 9 110072995 110072995 single base substitution G A intron_variant COCA-CN 9 110083551 110083551 single base substitution A T intron_variant COCA-CN 9 110084222 110084222 single base substitution T G intron_variant COCA-CN 9 110085741 110085741 single base substitution C G intron_variant COCA-CN 9 110089040 110089040 single base substitution G A intron_variant COCA-CN 9 110093971 110093971 single base substitution A C 3_prime_UTR_variant COCA-CN 9 110093971 110093971 single base substitution A C downstream_gene_variant COCA-CN 9 110093971 110093971 single base substitution A C missense_variant K104Q 310A>C EOPC-DE 9 110066214 110066214 single base substitution C T intron_variant EOPC-DE 9 110066214 110066214 single base substitution C T upstream_gene_variant ESAD-UK 9 110041047 110041047 single base substitution A T upstream_gene_variant ESAD-UK 9 110044464 110044464 single base substitution T C upstream_gene_variant ESAD-UK 9 110047287 110047287 single base substitution C T intron_variant ESAD-UK 9 110050125 110050125 single base substitution A C intron_variant ESAD-UK 9 110050894 110050894 insertion of <=200bp - T intron_variant ESAD-UK 9 110051579 110051579 single base substitution C T intron_variant ESAD-UK 9 110054282 110054282 single base substitution G T intron_variant ESAD-UK 9 110054564 110054564 single base substitution C T intron_variant ESAD-UK 9 110055473 110055473 single base substitution A G intron_variant ESAD-UK 9 110056040 110056040 single base substitution C T intron_variant ESAD-UK 9 110056276 110056276 single base substitution G A intron_variant ESAD-UK 9 110057368 110057368 insertion of <=200bp - G intron_variant ESAD-UK 9 110060088 110060088 single base substitution T C intron_variant ESAD-UK 9 110061891 110061891 single base substitution A T intron_variant ESAD-UK 9 110063898 110063898 single base substitution A G intron_variant ESAD-UK 9 110063898 110063898 single base substitution A G upstream_gene_variant ESAD-UK 9 110065023 110065023 single base substitution G A intron_variant ESAD-UK 9 110065023 110065023 single base substitution G A upstream_gene_variant ESAD-UK 9 110066133 110066133 single base substitution G A intron_variant ESAD-UK 9 110066133 110066133 single base substitution G A upstream_gene_variant ESAD-UK 9 110068362 110068362 single base substitution C A intron_variant ESAD-UK 9 110068362 110068362 single base substitution C A upstream_gene_variant ESAD-UK 9 110070057 110070057 single base substitution T C downstream_gene_variant ESAD-UK 9 110070057 110070057 single base substitution T C intron_variant ESAD-UK 9 110070403 110070403 single base substitution A T downstream_gene_variant ESAD-UK 9 110070403 110070403 single base substitution A T intron_variant ESAD-UK 9 110073394 110073394 single base substitution A C downstream_gene_variant ESAD-UK 9 110073394 110073394 single base substitution A C intron_variant ESAD-UK 9 110074052 110074052 deletion of <=200bp A - intron_variant ESAD-UK 9 110074264 110074264 single base substitution G A intron_variant ESAD-UK 9 110074547 110074547 deletion of <=200bp T - intron_variant ESAD-UK 9 110076571 110076571 deletion of <=200bp C - intron_variant ESAD-UK 9 110077460 110077460 single base substitution G A intron_variant ESAD-UK 9 110078535 110078535 single base substitution G A intron_variant ESAD-UK 9 110079078 110079078 single base substitution G T intron_variant ESAD-UK 9 110081292 110081292 single base substitution G A intron_variant ESAD-UK 9 110085588 110085588 single base substitution A C intron_variant ESAD-UK 9 110086459 110086459 deletion of <=200bp A - intron_variant ESAD-UK 9 110087363 110087363 single base substitution A G intron_variant ESAD-UK 9 110090704 110090704 single base substitution G A intron_variant ESAD-UK 9 110093630 110093630 insertion of <=200bp - A 3_prime_UTR_variant ESAD-UK 9 110093630 110093630 insertion of <=200bp - A downstream_gene_variant ESAD-UK 9 110093630 110093630 insertion of <=200bp - A intron_variant ESAD-UK 9 110095232 110095232 single base substitution A G downstream_gene_variant ESAD-UK 9 110097497 110097497 single base substitution G A downstream_gene_variant ESAD-UK 9 110097553 110097553 single base substitution A G downstream_gene_variant ESAD-UK 9 110098411 110098411 single base substitution C T downstream_gene_variant ESCA-CN 9 110068809 110068809 single base substitution C A downstream_gene_variant ESCA-CN 9 110068809 110068809 single base substitution C A synonymous_variant I126I 378C>A ESCA-CN 9 110068809 110068809 single base substitution C A synonymous_variant I54I 162C>A ESCA-CN 9 110068809 110068809 single base substitution C A upstream_gene_variant ESCA-CN 9 110093970 110093970 single base substitution C A 3_prime_UTR_variant ESCA-CN 9 110093970 110093970 single base substitution C A downstream_gene_variant ESCA-CN 9 110093970 110093970 single base substitution C A missense_variant N103K 309C>A GBM-US 9 110084309 110084309 single base substitution C T intron_variant GBM-US 9 110084309 110084309 single base substitution C T stop_gained Q171* 511C>T GBM-US 9 110084309 110084309 single base substitution C T stop_gained Q243* 727C>T GBM-US 9 110084381 110084383 deletion of <=200bp ACA - inframe_deletion T195 GBM-US 9 110084381 110084383 deletion of <=200bp ACA - inframe_deletion T267 GBM-US 9 110084381 110084383 deletion of <=200bp ACA - intron_variant KIRC-US 9 110084347 110084348 deletion of <=200bp GG - frameshift_variant VA183 KIRC-US 9 110084347 110084348 deletion of <=200bp GG - frameshift_variant VA255 KIRC-US 9 110084347 110084348 deletion of <=200bp GG - intron_variant KIRP-US 9 110091836 110091836 single base substitution G A intron_variant KIRP-US 9 110091836 110091836 single base substitution G A missense_variant G305R 913G>A KIRP-US 9 110091836 110091836 single base substitution G A missense_variant G377R 1129G>A LAML-KR 9 110064536 110064536 single base substitution T C intron_variant LAML-KR 9 110064536 110064536 single base substitution T C upstream_gene_variant LAML-KR 9 110070271 110070271 single base substitution C G downstream_gene_variant LAML-KR 9 110070271 110070271 single base substitution C G intron_variant LICA-CN 9 110068906 110068906 single base substitution A G downstream_gene_variant LICA-CN 9 110068906 110068906 single base substitution A G missense_variant T159A 475A>G LICA-CN 9 110068906 110068906 single base substitution A G missense_variant T28A 82A>G LICA-CN 9 110068906 110068906 single base substitution A G missense_variant T87A 259A>G LICA-FR 9 110050739 110050739 single base substitution G A intron_variant LICA-FR 9 110068144 110068144 single base substitution G T intron_variant LICA-FR 9 110068144 110068144 single base substitution G T upstream_gene_variant LICA-FR 9 110076308 110076308 single base substitution T C intron_variant LIHC-US 9 110091920 110091920 single base substitution A G intron_variant LIHC-US 9 110091920 110091920 single base substitution A G missense_variant N333D 997A>G LIHC-US 9 110091920 110091920 single base substitution A G missense_variant N405D 1213A>G LINC-JP 9 110043866 110043866 single base substitution T G upstream_gene_variant LINC-JP 9 110048068 110048068 single base substitution A C intron_variant LINC-JP 9 110057020 110057020 single base substitution A G intron_variant LINC-JP 9 110063560 110063560 single base substitution G C intron_variant LINC-JP 9 110064930 110064930 single base substitution G T intron_variant LINC-JP 9 110064930 110064930 single base substitution G T upstream_gene_variant LINC-JP 9 110064931 110064931 single base substitution T G intron_variant LINC-JP 9 110064931 110064931 single base substitution T G upstream_gene_variant LINC-JP 9 110074266 110074266 single base substitution A G intron_variant LINC-JP 9 110083584 110083584 single base substitution C T intron_variant LINC-JP 9 110084465 110084465 single base substitution T G intron_variant LINC-JP 9 110086237 110086237 single base substitution A G intron_variant LINC-JP 9 110086237 110086237 single base substitution A G missense_variant N223S 668A>G LINC-JP 9 110086237 110086237 single base substitution A G missense_variant N295S 884A>G LINC-JP 9 110094135 110094135 single base substitution A G 3_prime_UTR_variant LINC-JP 9 110094135 110094135 single base substitution A G downstream_gene_variant LINC-JP 9 110094197 110094197 single base substitution A G 3_prime_UTR_variant LINC-JP 9 110094197 110094197 single base substitution A G downstream_gene_variant LIRI-JP 9 110041893 110041893 single base substitution T C upstream_gene_variant LIRI-JP 9 110044222 110044222 single base substitution A G upstream_gene_variant LIRI-JP 9 110049447 110049447 single base substitution A G intron_variant LIRI-JP 9 110049692 110049692 single base substitution G A intron_variant LIRI-JP 9 110052428 110052428 single base substitution A C intron_variant LIRI-JP 9 110055212 110055212 single base substitution A G intron_variant LIRI-JP 9 110056362 110056362 single base substitution A G intron_variant LIRI-JP 9 110056894 110056894 single base substitution C G intron_variant LIRI-JP 9 110057072 110057072 single base substitution C A intron_variant LIRI-JP 9 110057680 110057680 single base substitution A G intron_variant LIRI-JP 9 110058080 110058092 deletion of <=200bp ACAGAGTGGTTGG - intron_variant LIRI-JP 9 110059761 110059761 single base substitution A T intron_variant LIRI-JP 9 110060127 110060127 single base substitution A G intron_variant LIRI-JP 9 110060173 110060177 deletion of <=200bp TTTTC - intron_variant LIRI-JP 9 110061845 110061845 single base substitution G T intron_variant LIRI-JP 9 110063686 110063688 deletion of <=200bp CTC - intron_variant LIRI-JP 9 110063914 110063914 single base substitution G T intron_variant LIRI-JP 9 110063914 110063914 single base substitution G T upstream_gene_variant LIRI-JP 9 110064812 110064812 single base substitution A G intron_variant LIRI-JP 9 110064812 110064812 single base substitution A G upstream_gene_variant LIRI-JP 9 110065655 110065655 single base substitution A G intron_variant LIRI-JP 9 110065655 110065655 single base substitution A G upstream_gene_variant LIRI-JP 9 110068071 110068071 single base substitution A G intron_variant LIRI-JP 9 110068071 110068071 single base substitution A G upstream_gene_variant LIRI-JP 9 110068325 110068336 deletion of <=200bp TTTATATCTATA - intron_variant LIRI-JP 9 110068325 110068336 deletion of <=200bp TTTATATCTATA - upstream_gene_variant LIRI-JP 9 110069037 110069037 single base substitution A T downstream_gene_variant LIRI-JP 9 110069037 110069037 single base substitution A T intron_variant LIRI-JP 9 110070270 110070270 single base substitution T A downstream_gene_variant LIRI-JP 9 110070270 110070270 single base substitution T A intron_variant LIRI-JP 9 110070380 110070380 single base substitution T C downstream_gene_variant LIRI-JP 9 110070380 110070380 single base substitution T C intron_variant LIRI-JP 9 110070427 110070427 single base substitution G A downstream_gene_variant LIRI-JP 9 110070427 110070427 single base substitution G A intron_variant LIRI-JP 9 110070467 110070467 single base substitution C A downstream_gene_variant LIRI-JP 9 110070467 110070467 single base substitution C A intron_variant LIRI-JP 9 110070785 110070785 single base substitution C T downstream_gene_variant LIRI-JP 9 110070785 110070785 single base substitution C T intron_variant LIRI-JP 9 110073206 110073206 single base substitution T A downstream_gene_variant LIRI-JP 9 110073206 110073206 single base substitution T A intron_variant LIRI-JP 9 110074014 110074014 single base substitution A G synonymous_variant A111A 333A>G LIRI-JP 9 110074014 110074014 single base substitution A G synonymous_variant A183A 549A>G LIRI-JP 9 110074014 110074014 single base substitution A G synonymous_variant A52A 156A>G LIRI-JP 9 110074389 110074389 single base substitution G T intron_variant LIRI-JP 9 110075392 110075392 single base substitution T C intron_variant LIRI-JP 9 110076264 110076264 single base substitution C A intron_variant LIRI-JP 9 110076265 110076265 single base substitution T C intron_variant LIRI-JP 9 110081892 110081892 single base substitution G A intron_variant LIRI-JP 9 110083258 110083258 single base substitution A G intron_variant LIRI-JP 9 110083360 110083360 single base substitution C A intron_variant LIRI-JP 9 110083608 110083608 single base substitution A G intron_variant LIRI-JP 9 110087168 110087168 single base substitution A G intron_variant LIRI-JP 9 110087168 110087168 single base substitution A G synonymous_variant Q261Q 783A>G LIRI-JP 9 110087168 110087168 single base substitution A G synonymous_variant Q333Q 999A>G LIRI-JP 9 110087964 110087964 single base substitution C T intron_variant LIRI-JP 9 110089007 110089007 single base substitution T C intron_variant LIRI-JP 9 110089391 110089391 single base substitution C A intron_variant LIRI-JP 9 110092679 110092679 single base substitution C G 3_prime_UTR_variant LIRI-JP 9 110092679 110092679 single base substitution C G downstream_gene_variant LIRI-JP 9 110092679 110092679 single base substitution C G intron_variant LIRI-JP 9 110094906 110094906 single base substitution T G downstream_gene_variant LIRI-JP 9 110095370 110095370 single base substitution A C downstream_gene_variant LIRI-JP 9 110096011 110096011 single base substitution A G downstream_gene_variant LIRI-JP 9 110097232 110097232 single base substitution G C downstream_gene_variant LIRI-JP 9 110099104 110099104 single base substitution A G downstream_gene_variant LUSC-KR 9 110042073 110042073 single base substitution T C upstream_gene_variant LUSC-KR 9 110057275 110057275 single base substitution A G intron_variant LUSC-KR 9 110058645 110058645 single base substitution C T intron_variant LUSC-KR 9 110063824 110063824 single base substitution A G intron_variant LUSC-KR 9 110063824 110063824 single base substitution A G upstream_gene_variant LUSC-KR 9 110077608 110077608 single base substitution G A intron_variant LUSC-KR 9 110078134 110078134 single base substitution A T intron_variant LUSC-KR 9 110081430 110081430 single base substitution G T intron_variant LUSC-KR 9 110087405 110087405 single base substitution G T intron_variant MALY-DE 9 110041211 110041211 single base substitution T A upstream_gene_variant MALY-DE 9 110041224 110041224 single base substitution T C upstream_gene_variant MALY-DE 9 110063320 110063320 single base substitution G C intron_variant MALY-DE 9 110074019 110074022 deletion of <=200bp GTAA - splice_donor_variant MALY-DE 9 110075084 110075084 single base substitution G C intron_variant MALY-DE 9 110077649 110077649 single base substitution G C intron_variant MALY-DE 9 110080458 110080458 single base substitution A T intron_variant MALY-DE 9 110083527 110083551 deletion of <=200bp TGAGATACTTTAAGTATCTCATTTA - intron_variant MALY-DE 9 110083823 110083823 single base substitution T G intron_variant MALY-DE 9 110089962 110089962 single base substitution C T intron_variant MALY-DE 9 110095499 110095499 single base substitution C A downstream_gene_variant MALY-DE 9 110098913 110098913 single base substitution G A downstream_gene_variant MELA-AU 9 110042477 110042477 single base substitution G A upstream_gene_variant MELA-AU 9 110044041 110044041 single base substitution C T upstream_gene_variant MELA-AU 9 110044963 110044963 single base substitution C T upstream_gene_variant MELA-AU 9 110045484 110045484 single base substitution C T 5_prime_UTR_variant MELA-AU 9 110045484 110045484 single base substitution C T upstream_gene_variant MELA-AU 9 110046553 110046553 single base substitution C T intron_variant MELA-AU 9 110046553 110046553 single base substitution C T upstream_gene_variant MELA-AU 9 110047804 110047804 single base substitution G A intron_variant MELA-AU 9 110049331 110049331 single base substitution G A intron_variant MELA-AU 9 110051440 110051440 single base substitution C T intron_variant MELA-AU 9 110051687 110051687 single base substitution C T intron_variant MELA-AU 9 110052662 110052662 single base substitution C T intron_variant MELA-AU 9 110053271 110053271 single base substitution G A intron_variant MELA-AU 9 110056357 110056357 single base substitution C T intron_variant MELA-AU 9 110058616 110058616 single base substitution C T intron_variant MELA-AU 9 110058745 110058745 single base substitution G T intron_variant MELA-AU 9 110059453 110059453 single base substitution A T intron_variant MELA-AU 9 110059556 110059556 single base substitution T C intron_variant MELA-AU 9 110059558 110059558 single base substitution T C intron_variant MELA-AU 9 110059662 110059662 single base substitution C T intron_variant MELA-AU 9 110060413 110060413 single base substitution G A intron_variant MELA-AU 9 110060612 110060612 single base substitution T A intron_variant MELA-AU 9 110061106 110061106 single base substitution A G intron_variant MELA-AU 9 110062939 110062939 single base substitution T G intron_variant MELA-AU 9 110064164 110064164 single base substitution C T intron_variant MELA-AU 9 110064164 110064164 single base substitution C T upstream_gene_variant MELA-AU 9 110064323 110064323 single base substitution C T 5_prime_UTR_variant MELA-AU 9 110064323 110064323 single base substitution C T synonymous_variant I31I 93C>T MELA-AU 9 110064323 110064323 single base substitution C T synonymous_variant I52I 156C>T MELA-AU 9 110064323 110064323 single base substitution C T upstream_gene_variant MELA-AU 9 110065352 110065352 single base substitution C A intron_variant MELA-AU 9 110065352 110065352 single base substitution C A upstream_gene_variant MELA-AU 9 110065569 110065569 single base substitution C T intron_variant MELA-AU 9 110065569 110065569 single base substitution C T upstream_gene_variant MELA-AU 9 110066978 110066978 single base substitution C T intron_variant MELA-AU 9 110066978 110066978 single base substitution C T upstream_gene_variant MELA-AU 9 110067453 110067453 single base substitution C T intron_variant MELA-AU 9 110067453 110067453 single base substitution C T upstream_gene_variant MELA-AU 9 110068163 110068163 single base substitution G A intron_variant MELA-AU 9 110068163 110068163 single base substitution G A upstream_gene_variant MELA-AU 9 110069427 110069427 single base substitution C T downstream_gene_variant MELA-AU 9 110069427 110069427 single base substitution C T intron_variant MELA-AU 9 110069883 110069883 single base substitution A G downstream_gene_variant MELA-AU 9 110069883 110069883 single base substitution A G intron_variant MELA-AU 9 110069984 110069984 single base substitution C T downstream_gene_variant MELA-AU 9 110069984 110069984 single base substitution C T intron_variant MELA-AU 9 110070989 110070989 single base substitution C G downstream_gene_variant MELA-AU 9 110070989 110070989 single base substitution C G intron_variant MELA-AU 9 110071207 110071207 single base substitution C T downstream_gene_variant MELA-AU 9 110071207 110071207 single base substitution C T intron_variant MELA-AU 9 110071510 110071510 single base substitution C T downstream_gene_variant MELA-AU 9 110071510 110071510 single base substitution C T intron_variant MELA-AU 9 110071576 110071576 single base substitution C T downstream_gene_variant MELA-AU 9 110071576 110071576 single base substitution C T intron_variant MELA-AU 9 110072119 110072119 single base substitution G A downstream_gene_variant MELA-AU 9 110072119 110072119 single base substitution G A intron_variant MELA-AU 9 110074086 110074086 single base substitution C T intron_variant MELA-AU 9 110074224 110074224 single base substitution T C intron_variant MELA-AU 9 110074621 110074621 single base substitution C T intron_variant MELA-AU 9 110075264 110075264 single base substitution C T intron_variant MELA-AU 9 110075509 110075509 single base substitution T C intron_variant MELA-AU 9 110075928 110075928 single base substitution C T intron_variant MELA-AU 9 110076633 110076633 single base substitution C T intron_variant MELA-AU 9 110077066 110077066 single base substitution C T intron_variant MELA-AU 9 110077215 110077215 single base substitution C A intron_variant MELA-AU 9 110078371 110078371 single base substitution A G intron_variant MELA-AU 9 110079151 110079151 insertion of <=200bp - A intron_variant MELA-AU 9 110079932 110079933 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 110080531 110080531 single base substitution C T intron_variant MELA-AU 9 110080568 110080568 single base substitution C T intron_variant MELA-AU 9 110080745 110080745 single base substitution C T intron_variant MELA-AU 9 110081415 110081415 insertion of <=200bp - TTTC intron_variant MELA-AU 9 110081828 110081828 single base substitution G C intron_variant MELA-AU 9 110082454 110082454 single base substitution T C intron_variant MELA-AU 9 110085714 110085714 single base substitution C T intron_variant MELA-AU 9 110086518 110086518 single base substitution T G intron_variant MELA-AU 9 110087295 110087295 single base substitution A G intron_variant MELA-AU 9 110087858 110087858 single base substitution T C intron_variant MELA-AU 9 110088945 110088945 single base substitution C T intron_variant MELA-AU 9 110089155 110089155 single base substitution C T intron_variant MELA-AU 9 110089883 110089883 single base substitution C T intron_variant MELA-AU 9 110091500 110091500 single base substitution A G intron_variant MELA-AU 9 110092217 110092217 single base substitution T A 3_prime_UTR_variant MELA-AU 9 110092217 110092217 single base substitution T A downstream_gene_variant MELA-AU 9 110092217 110092217 single base substitution T A intron_variant MELA-AU 9 110093012 110093012 single base substitution T C 3_prime_UTR_variant MELA-AU 9 110093012 110093012 single base substitution T C downstream_gene_variant MELA-AU 9 110093012 110093012 single base substitution T C intron_variant MELA-AU 9 110093549 110093549 single base substitution C T 3_prime_UTR_variant MELA-AU 9 110093549 110093549 single base substitution C T downstream_gene_variant MELA-AU 9 110093549 110093549 single base substitution C T intron_variant MELA-AU 9 110094140 110094141 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 9 110094140 110094141 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 9 110094416 110094416 single base substitution C T 3_prime_UTR_variant MELA-AU 9 110094416 110094416 single base substitution C T downstream_gene_variant MELA-AU 9 110094554 110094554 single base substitution C A downstream_gene_variant MELA-AU 9 110094864 110094864 single base substitution C T downstream_gene_variant MELA-AU 9 110094875 110094875 single base substitution C T downstream_gene_variant MELA-AU 9 110095552 110095552 single base substitution C T downstream_gene_variant MELA-AU 9 110096390 110096390 single base substitution C T downstream_gene_variant MELA-AU 9 110097217 110097217 single base substitution A G downstream_gene_variant MELA-AU 9 110098079 110098079 single base substitution C T downstream_gene_variant ORCA-IN 9 110049514 110049514 single base substitution G T intron_variant ORCA-IN 9 110072334 110072334 single base substitution A G downstream_gene_variant ORCA-IN 9 110072334 110072334 single base substitution A G intron_variant ORCA-IN 9 110074130 110074130 single base substitution C T intron_variant ORCA-IN 9 110079397 110079397 single base substitution G T intron_variant ORCA-IN 9 110091856 110091856 single base substitution G C intron_variant ORCA-IN 9 110091856 110091856 single base substitution G C synonymous_variant V311V 933G>C ORCA-IN 9 110091856 110091856 single base substitution G C synonymous_variant V383V 1149G>C OV-AU 9 110049201 110049201 single base substitution A G intron_variant OV-AU 9 110058115 110058115 single base substitution C A intron_variant OV-AU 9 110067345 110067345 single base substitution G A intron_variant OV-AU 9 110067345 110067345 single base substitution G A upstream_gene_variant OV-AU 9 110079972 110079972 single base substitution A G intron_variant OV-AU 9 110090902 110090902 single base substitution C G intron_variant OV-AU 9 110093433 110093433 single base substitution G A 3_prime_UTR_variant OV-AU 9 110093433 110093433 single base substitution G A downstream_gene_variant OV-AU 9 110093433 110093433 single base substitution G A intron_variant OV-US 9 110081063 110081063 single base substitution C T missense_variant T123I 368C>T OV-US 9 110081063 110081063 single base substitution C T missense_variant T195I 584C>T OV-US 9 110081063 110081063 single base substitution C T missense_variant T64I 191C>T PACA-AU 9 110042047 110042047 single base substitution T C upstream_gene_variant PACA-AU 9 110042132 110042132 single base substitution G C upstream_gene_variant PACA-AU 9 110047147 110047147 single base substitution T A 5_prime_UTR_variant PACA-AU 9 110047147 110047147 single base substitution T A intron_variant PACA-AU 9 110048505 110048505 single base substitution T C intron_variant PACA-AU 9 110054814 110054814 single base substitution A T intron_variant PACA-AU 9 110055490 110055490 single base substitution C G intron_variant PACA-AU 9 110056783 110056783 single base substitution T G intron_variant PACA-AU 9 110059745 110059745 single base substitution C T intron_variant PACA-AU 9 110060184 110060184 single base substitution T G intron_variant PACA-AU 9 110063636 110063636 single base substitution C T intron_variant PACA-AU 9 110064428 110064428 single base substitution G A intron_variant PACA-AU 9 110064428 110064428 single base substitution G A upstream_gene_variant PACA-AU 9 110067120 110067120 single base substitution C A intron_variant PACA-AU 9 110067120 110067120 single base substitution C A upstream_gene_variant PACA-AU 9 110073871 110073871 single base substitution G C downstream_gene_variant PACA-AU 9 110073871 110073871 single base substitution G C intron_variant PACA-AU 9 110075967 110075967 single base substitution C T intron_variant PACA-AU 9 110080819 110080819 single base substitution C T intron_variant PACA-AU 9 110084539 110084539 single base substitution G A intron_variant PACA-AU 9 110084771 110084771 single base substitution G T intron_variant PACA-AU 9 110087512 110087512 single base substitution T G intron_variant PACA-AU 9 110090234 110090234 single base substitution G A intron_variant PACA-AU 9 110094210 110094210 single base substitution G T 3_prime_UTR_variant PACA-AU 9 110094210 110094210 single base substitution G T downstream_gene_variant PACA-CA 9 110046928 110046928 single base substitution G T intron_variant PACA-CA 9 110046928 110046928 single base substitution G T upstream_gene_variant PACA-CA 9 110049169 110049169 single base substitution C T intron_variant PACA-CA 9 110052851 110052851 single base substitution G T intron_variant PACA-CA 9 110053296 110053296 single base substitution C G intron_variant PACA-CA 9 110055198 110055198 single base substitution T G intron_variant PACA-CA 9 110059619 110059619 single base substitution T C intron_variant PACA-CA 9 110066719 110066719 deletion of <=200bp T - intron_variant PACA-CA 9 110066719 110066719 deletion of <=200bp T - upstream_gene_variant PACA-CA 9 110067608 110067608 single base substitution A G intron_variant PACA-CA 9 110067608 110067608 single base substitution A G upstream_gene_variant PACA-CA 9 110068641 110068641 single base substitution T G intron_variant PACA-CA 9 110068641 110068641 single base substitution T G upstream_gene_variant PACA-CA 9 110069215 110069215 single base substitution C T downstream_gene_variant PACA-CA 9 110069215 110069215 single base substitution C T intron_variant PACA-CA 9 110070098 110070098 single base substitution C T downstream_gene_variant PACA-CA 9 110070098 110070098 single base substitution C T intron_variant PACA-CA 9 110073137 110073137 single base substitution A G downstream_gene_variant PACA-CA 9 110073137 110073137 single base substitution A G intron_variant PACA-CA 9 110075140 110075140 insertion of <=200bp - GTCA intron_variant PACA-CA 9 110081553 110081553 single base substitution A C intron_variant PACA-CA 9 110081613 110081613 single base substitution A T intron_variant PACA-CA 9 110086511 110086511 single base substitution A C intron_variant PACA-CA 9 110093916 110093916 single base substitution C A 3_prime_UTR_variant PACA-CA 9 110093916 110093916 single base substitution C A downstream_gene_variant PACA-CA 9 110093916 110093916 single base substitution C A intron_variant PACA-CA 9 110099098 110099098 single base substitution C A downstream_gene_variant PAEN-AU 9 110046113 110046113 single base substitution C T intron_variant PAEN-AU 9 110046113 110046113 single base substitution C T upstream_gene_variant PAEN-AU 9 110058383 110058383 single base substitution G A intron_variant PAEN-AU 9 110075106 110075106 single base substitution A T intron_variant PAEN-IT 9 110046273 110046273 single base substitution G C intron_variant PAEN-IT 9 110046273 110046273 single base substitution G C upstream_gene_variant PAEN-IT 9 110085864 110085864 single base substitution A G intron_variant PBCA-DE 9 110040920 110040920 single base substitution C T upstream_gene_variant PBCA-DE 9 110049011 110049011 single base substitution G T intron_variant PBCA-DE 9 110055342 110055342 insertion of <=200bp - G intron_variant PBCA-DE 9 110065520 110065520 single base substitution A G intron_variant PBCA-DE 9 110065520 110065520 single base substitution A G upstream_gene_variant PBCA-DE 9 110066676 110066676 single base substitution C A intron_variant PBCA-DE 9 110066676 110066676 single base substitution C A upstream_gene_variant PBCA-DE 9 110069586 110069586 single base substitution T G downstream_gene_variant PBCA-DE 9 110069586 110069586 single base substitution T G intron_variant PBCA-DE 9 110072616 110072616 insertion of <=200bp - A downstream_gene_variant PBCA-DE 9 110072616 110072616 insertion of <=200bp - A intron_variant PBCA-DE 9 110074243 110074243 deletion of <=200bp G - intron_variant PBCA-DE 9 110077665 110077665 single base substitution A G intron_variant PBCA-DE 9 110080233 110080233 single base substitution G A intron_variant PBCA-DE 9 110094250 110094250 single base substitution T A 3_prime_UTR_variant PBCA-DE 9 110094250 110094250 single base substitution T A downstream_gene_variant PRAD-CA 9 110069206 110069206 single base substitution G T downstream_gene_variant PRAD-CA 9 110069206 110069206 single base substitution G T intron_variant PRAD-CA 9 110077595 110077595 single base substitution A G intron_variant PRAD-UK 9 110042492 110042492 single base substitution G C upstream_gene_variant PRAD-UK 9 110053502 110053502 single base substitution A G intron_variant PRAD-UK 9 110053701 110053701 single base substitution A G intron_variant PRAD-UK 9 110061125 110061125 insertion of <=200bp - A intron_variant PRAD-UK 9 110061132 110061132 insertion of <=200bp - A intron_variant PRAD-UK 9 110061881 110061881 single base substitution A C intron_variant PRAD-UK 9 110066844 110066844 single base substitution C G intron_variant PRAD-UK 9 110066844 110066844 single base substitution C G upstream_gene_variant PRAD-UK 9 110070403 110070403 single base substitution A T downstream_gene_variant PRAD-UK 9 110070403 110070403 single base substitution A T intron_variant PRAD-UK 9 110077794 110077794 insertion of <=200bp - T intron_variant PRAD-UK 9 110083893 110083893 single base substitution A T intron_variant PRAD-UK 9 110087201 110087201 single base substitution T A intron_variant PRAD-UK 9 110087201 110087201 single base substitution T A synonymous_variant G272G 816T>A PRAD-UK 9 110087201 110087201 single base substitution T A synonymous_variant G344G 1032T>A READ-US 9 110087203 110087203 single base substitution G A intron_variant READ-US 9 110087203 110087203 single base substitution G A missense_variant G273D 818G>A READ-US 9 110087203 110087203 single base substitution G A missense_variant G345D 1034G>A RECA-EU 9 110053433 110053433 single base substitution G A intron_variant RECA-EU 9 110056459 110056459 single base substitution G T intron_variant RECA-EU 9 110078184 110078184 single base substitution A G intron_variant RECA-EU 9 110082152 110082152 single base substitution A G intron_variant RECA-EU 9 110082331 110082331 single base substitution C G intron_variant RECA-EU 9 110091555 110091555 single base substitution A G intron_variant RECA-EU 9 110091974 110091974 single base substitution C T 3_prime_UTR_variant RECA-EU 9 110091974 110091974 single base substitution C T intron_variant RECA-EU 9 110097213 110097213 single base substitution T A downstream_gene_variant RECA-EU 9 110098246 110098246 single base substitution C G downstream_gene_variant SKCA-BR 9 110040462 110040462 single base substitution G A upstream_gene_variant SKCA-BR 9 110040995 110040996 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 9 110041129 110041129 single base substitution C T upstream_gene_variant SKCA-BR 9 110045791 110045791 single base substitution A C 5_prime_UTR_variant SKCA-BR 9 110045791 110045791 single base substitution A C intron_variant SKCA-BR 9 110045791 110045791 single base substitution A C upstream_gene_variant SKCA-BR 9 110046170 110046170 single base substitution A G intron_variant SKCA-BR 9 110046170 110046170 single base substitution A G upstream_gene_variant SKCA-BR 9 110047856 110047856 single base substitution G C intron_variant SKCA-BR 9 110051305 110051349 deletion of <=200bp TTCCCTCCCTTCCTCTCTCCCTTCCTCCCTCCCTTCTTCCCTTCC - intron_variant SKCA-BR 9 110051320 110051320 single base substitution T C intron_variant SKCA-BR 9 110051367 110051367 single base substitution C T intron_variant SKCA-BR 9 110055563 110055563 single base substitution C T intron_variant SKCA-BR 9 110058448 110058448 single base substitution C T intron_variant SKCA-BR 9 110060006 110060006 single base substitution C T intron_variant SKCA-BR 9 110060014 110060014 single base substitution C T intron_variant SKCA-BR 9 110067677 110067677 single base substitution A T intron_variant SKCA-BR 9 110067677 110067677 single base substitution A T upstream_gene_variant SKCA-BR 9 110068324 110068334 deletion of <=200bp GTTTATATCTA - intron_variant SKCA-BR 9 110068324 110068334 deletion of <=200bp GTTTATATCTA - upstream_gene_variant SKCA-BR 9 110068344 110068344 single base substitution A C intron_variant SKCA-BR 9 110068344 110068344 single base substitution A C upstream_gene_variant SKCA-BR 9 110068366 110068366 insertion of <=200bp - ATACACTC intron_variant SKCA-BR 9 110068366 110068366 insertion of <=200bp - ATACACTC upstream_gene_variant SKCA-BR 9 110069203 110069206 deletion of <=200bp TTTG - downstream_gene_variant SKCA-BR 9 110069203 110069206 deletion of <=200bp TTTG - intron_variant SKCA-BR 9 110070403 110070403 single base substitution A T downstream_gene_variant SKCA-BR 9 110070403 110070403 single base substitution A T intron_variant SKCA-BR 9 110072231 110072232 deletion of <=200bp AC - downstream_gene_variant SKCA-BR 9 110072231 110072232 deletion of <=200bp AC - intron_variant SKCA-BR 9 110072232 110072232 single base substitution C A downstream_gene_variant SKCA-BR 9 110072232 110072232 single base substitution C A intron_variant SKCA-BR 9 110075474 110075474 single base substitution T A intron_variant SKCA-BR 9 110075499 110075499 single base substitution C T intron_variant SKCA-BR 9 110075524 110075524 single base substitution C T intron_variant SKCA-BR 9 110081401 110081402 deletion of <=200bp TC - intron_variant SKCA-BR 9 110081408 110081409 deletion of <=200bp TC - intron_variant SKCA-BR 9 110081412 110081412 insertion of <=200bp - TTTTTC intron_variant SKCA-BR 9 110087188 110087188 single base substitution G A intron_variant SKCA-BR 9 110087188 110087188 single base substitution G A missense_variant G268E 803G>A SKCA-BR 9 110087188 110087188 single base substitution G A missense_variant G340E 1019G>A SKCA-BR 9 110089452 110089452 single base substitution T C intron_variant SKCA-BR 9 110090664 110090664 single base substitution G A intron_variant SKCA-BR 9 110095142 110095142 single base substitution C T downstream_gene_variant SKCA-BR 9 110097566 110097566 single base substitution T A downstream_gene_variant SKCM-US 9 110081045 110081045 single base substitution C A missense_variant S117Y 350C>A SKCM-US 9 110081045 110081045 single base substitution C A missense_variant S189Y 566C>A SKCM-US 9 110081045 110081045 single base substitution C A missense_variant S58Y 173C>A SKCM-US 9 110086177 110086177 single base substitution C T intron_variant SKCM-US 9 110086177 110086177 single base substitution C T missense_variant P203L 608C>T SKCM-US 9 110086177 110086177 single base substitution C T missense_variant P275L 824C>T SKCM-US 9 110086240 110086240 single base substitution C T intron_variant SKCM-US 9 110086240 110086240 single base substitution C T missense_variant P224L 671C>T SKCM-US 9 110086240 110086240 single base substitution C T missense_variant P296L 887C>T STAD-US 9 110062486 110062486 deletion of <=200bp A - 5_prime_UTR_variant STAD-US 9 110062486 110062486 deletion of <=200bp A - frameshift_variant Q23 STAD-US 9 110062486 110062486 deletion of <=200bp A - frameshift_variant Q44 STAD-US 9 110081036 110081036 single base substitution C T missense_variant T114M 341C>T STAD-US 9 110081036 110081036 single base substitution C T missense_variant T186M 557C>T STAD-US 9 110081036 110081036 single base substitution C T missense_variant T55M 164C>T STAD-US 9 110081129 110081129 single base substitution A G missense_variant N145S 434A>G STAD-US 9 110081129 110081129 single base substitution A G missense_variant N217S 650A>G STAD-US 9 110081129 110081129 single base substitution A G missense_variant N86S 257A>G THCA-SA 9 110092856 110092856 single base substitution C T 3_prime_UTR_variant THCA-SA 9 110092856 110092856 single base substitution C T downstream_gene_variant THCA-SA 9 110092856 110092856 single base substitution C T intron_variant THCA-US 9 110074019 110074019 single base substitution G T splice_donor_variant UCEC-US 9 110062463 110062463 single base substitution A C 5_prime_UTR_variant UCEC-US 9 110062463 110062463 single base substitution A C missense_variant K15N 45A>C UCEC-US 9 110062463 110062463 single base substitution A C missense_variant K36N 108A>C UCEC-US 9 110064335 110064335 single base substitution T C 5_prime_UTR_variant UCEC-US 9 110064335 110064335 single base substitution T C synonymous_variant D35D 105T>C UCEC-US 9 110064335 110064335 single base substitution T C synonymous_variant D56D 168T>C UCEC-US 9 110064335 110064335 single base substitution T C upstream_gene_variant UCEC-US 9 110068824 110068824 single base substitution G A 5_prime_UTR_variant UCEC-US 9 110068824 110068824 single base substitution G A downstream_gene_variant UCEC-US 9 110068824 110068824 single base substitution G A synonymous_variant A131A 393G>A UCEC-US 9 110068824 110068824 single base substitution G A synonymous_variant A59A 177G>A UCEC-US 9 110068897 110068897 single base substitution C T downstream_gene_variant UCEC-US 9 110068897 110068897 single base substitution C T missense_variant P156S 466C>T UCEC-US 9 110068897 110068897 single base substitution C T missense_variant P25S 73C>T UCEC-US 9 110068897 110068897 single base substitution C T missense_variant P84S 250C>T UCEC-US 9 110074008 110074008 single base substitution G A synonymous_variant T109T 327G>A UCEC-US 9 110074008 110074008 single base substitution G A synonymous_variant T181T 543G>A UCEC-US 9 110074008 110074008 single base substitution G A synonymous_variant T50T 150G>A UCEC-US 9 110081148 110081148 single base substitution G A synonymous_variant E151E 453G>A UCEC-US 9 110081148 110081148 single base substitution G A synonymous_variant E223E 669G>A UCEC-US 9 110081148 110081148 single base substitution G A synonymous_variant E92E 276G>A UCEC-US 9 110087223 110087223 single base substitution G T intron_variant UCEC-US 9 110087223 110087223 single base substitution G T missense_variant A280S 838G>T UCEC-US 9 110087223 110087223 single base substitution G T missense_variant A352S 1054G>T UCEC-US 9 110091855 110091855 single base substitution T C intron_variant UCEC-US 9 110091855 110091855 single base substitution T C missense_variant V311A 932T>C UCEC-US 9 110091855 110091855 single base substitution T C missense_variant V383A 1148T>C UCEC-US 9 110091866 110091866 single base substitution T C intron_variant UCEC-US 9 110091866 110091866 single base substitution T C missense_variant Y315H 943T>C UCEC-US 9 110091866 110091866 single base substitution T C missense_variant Y387H 1159T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand RK084_C01 COSM1635961 c.549A>G p.A183A Substitution - coding silent 9:107311733-107311733 + TCGA-ER-A195-06 COSM3652681 c.824C>T p.P275L Substitution - Missense 9:107323896-107323896 + tumor_4119279 COSM5947087 c.553+1_553+4delGTAA p.? Unknown 9:107311738-107311741 + HDC87 COSM4637211 c.513T>C p.S171S Substitution - coding silent 9:107311697-107311697 + CLN4 COSM5024704 c.247C>T p.P83S Substitution - Missense 9:107306397-107306397 + TCGA-AC-A23H-01 COSM3847284 c.1180G>A p.E394K Substitution - Missense 9:107329606-107329606 + TCGA-AP-A059-01 COSM1103637 c.669G>A p.E223E Substitution - coding silent 9:107318867-107318867 + TCGA-BR-4362-01 COSM284442 c.557C>T p.T186M Substitution - Missense 9:107318755-107318755 + ORL-48 COSM4596660 c.413C>G p.A138G Substitution - Missense 9:107306563-107306563 + TCGA-BJ-A4O9-01 COSM3375028 c.553+1G>T p.? Unknown 9:107311738-107311738 + TCGA-D1-A17Q-01 COSM1103633 c.168T>C p.D56D Substitution - coding silent 9:107302054-107302054 + BN49T COSM1624401 c.884A>G p.N295S Substitution - Missense 9:107323956-107323956 + TCGA-AA-3684-01 COSM293155 c.1157C>T p.A386V Substitution - Missense 9:107329583-107329583 + PD7316a COSM5802179 c.697_700delAGAG p.R233fs*55 Deletion - Frameshift 9:107321998-107322001 + 587332 COSM1222993 c.1129G>A p.G377R Substitution - Missense 9:107329555-107329555 + Sample_1 COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + 2492726 COSM5725314 c.561T>C p.G187G Substitution - coding silent 9:107318759-107318759 + TCGA-A5-A0GP-01 COSM1103632 c.108A>C p.K36N Substitution - Missense 9:107300182-107300182 + 587332 COSM1222992 c.575A>T p.N192I Substitution - Missense 9:107318773-107318773 + TCGA-AA-A010-01 COSM284442 c.557C>T p.T186M Substitution - Missense 9:107318755-107318755 + TCGA-DR-A0ZM-01 COSM461380 c.242C>G p.S81C Substitution - Missense 9:107306392-107306392 + RMS111_ COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + RK122_C01 COSM3745745 c.999A>G p.Q333Q Substitution - coding silent 9:107324887-107324887 + RMS109_ COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + CSCC-10-T COSM4567444 c.714_715GG>AA p.V239I Substitution - Missense 9:107322015-107322016 + HN_62854 COSM121696 c.1149G>A p.V383V Substitution - coding silent 9:107329575-107329575 + TCGA-AR-A2LE-01 COSM3847282 c.586G>A p.E196K Substitution - Missense 9:107318784-107318784 + HCT116 COSM3168734 c.942T>C p.L314L Substitution - coding silent 9:107324014-107324014 + LIM2405 COSM3168729 c.799_801delACA p.T269delT Deletion - In frame 9:107322100-107322102 + TCGA-13-1411-01 COSM76155 c.584C>T p.T195I Substitution - Missense 9:107318782-107318782 + TCGA-AP-A0LM-01 COSM1103634 c.393G>A p.A131A Substitution - coding silent 9:107306543-107306543 + OSCC-GB_01380111 COSM5953840 c.1149G>C p.V383V Substitution - coding silent 9:107329575-107329575 + TCGA-AP-A059-01 COSM1103638 c.1054G>T p.A352S Substitution - Missense 9:107324942-107324942 + LUAD-RT-S01477 COSM377773 c.697A>T p.R233* Substitution - Nonsense 9:107321998-107321998 + PDA_076 COSM5002222 c.1117-1_1117insT p.L373fs*8 Unknown 9:107329542-107329543 + LUAD-CHTN-3090346 COSM391266 c.1096_1097insA p.E368fs*13 Insertion - Frameshift 9:107324984-107324985 + TCGA-AP-A0LM-01 COSM1103636 c.543G>A p.T181T Substitution - coding silent 9:107311727-107311727 + TCGA-02-0047 COSM2157820 c.768_769insG p.A257fs*21 Insertion - Frameshift 9:107322069-107322070 + V-PH-34T COSM4770545 c.58delG p.E20fs*4 Deletion - Frameshift 9:107283687-107283687 + TCGA-BH-A0WA-01 COSM455109 c.866G>A p.R289K Substitution - Missense 9:107323938-107323938 + TCGA-AM-5820-01 COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + RMS10_ COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + TCGA-DD-A39Y-01 COSM4934554 c.1213A>G p.N405D Substitution - Missense 9:107329639-107329639 + cSCCP8 COSM140627 c.508G>A p.D170N Substitution - Missense 9:107311692-107311692 + 08-P1004 COSM4588328 c.1206A>G p.L402L Substitution - coding silent 9:107329632-107329632 + TCGA-EE-A2MJ-06 COSM3652682 c.887C>T p.P296L Substitution - Missense 9:107323959-107323959 + WA22 COSM241345 c.589A>G p.I197V Substitution - Missense 9:107318787-107318787 + EGC28 COSM5063488 c.482C>T p.P161L Substitution - Missense 9:107306632-107306632 + TCGA-EK-A3GK-01 COSM4853535 c.325C>T p.Q109* Substitution - Nonsense 9:107306475-107306475 + 587376 COSM1222994 c.181G>T p.E61* Substitution - Nonsense 9:107302067-107302067 + TCGA-FW-A3R5-06 COSM3925855 c.566C>A p.S189Y Substitution - Missense 9:107318764-107318764 + TCGA-EK-A2R8-01 COSM4822540 c.1016G>C p.G339A Substitution - Missense 9:107324904-107324904 + TCGA-A8-A0A6-01 COSM3847281 c.358A>C p.T120P Substitution - Missense 9:107306508-107306508 + TCGA-GL-8500-01 COSM1222993 c.1129G>A p.G377R Substitution - Missense 9:107329555-107329555 + Pat_44_B COSM5875301 c.517C>T p.R173W Substitution - Missense 9:107311701-107311701 + CT-TC COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + HCC123T COSM5816929 c.475A>G p.T159A Substitution - Missense 9:107306625-107306625 + 0006_CRUK_PC_0006_T3_DNA COSM3849723 c.1032T>A p.G344G Substitution - coding silent 9:107324920-107324920 + TCGA-BS-A0UF-01 COSM1103640 c.1159T>C p.Y387H Substitution - Missense 9:107329585-107329585 + YUOTHO COSM5410099 c.630C>T p.A210A Substitution - coding silent 9:107318828-107318828 + PD4132a COSM163908 c.877C>T p.Q293* Substitution - Nonsense 9:107323949-107323949 + TCGA-06-0214-01 COSM3413227 c.727C>T p.Q243* Substitution - Nonsense 9:107322028-107322028 + RMS77_ COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + BN49 COSM1624401 c.884A>G p.N295S Substitution - Missense 9:107323956-107323956 + TCGA-F5-6814-01 COSM3432744 c.1034G>A p.G345D Substitution - Missense 9:107324922-107324922 + TCGA-MU-A51Y-01 COSM4836553 c.923G>A p.R308Q Substitution - Missense 9:107323995-107323995 + TCGA-DK-A3WW-01 COSM3779515 c.915G>C p.Q305H Substitution - Missense 9:107323987-107323987 + TCGA-AC-A23H-01 COSM3847283 c.934C>G p.Q312E Substitution - Missense 9:107324006-107324006 + PT36 COSM5915881 c.1066C>T p.H356Y Substitution - Missense 9:107324954-107324954 + STC263 COSM5063490 c.905T>A p.L302* Substitution - Nonsense 9:107323977-107323977 + 587376 COSM1222995 c.755C>A p.S252Y Substitution - Missense 9:107322056-107322056 + SMS-CTR COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + TCGA-AD-5900-01 COSM1459176 c.344C>A p.P115H Substitution - Missense 9:107306494-107306494 + TCGA-CD-A4MG-01 COSM3902834 c.650A>G p.N217S Substitution - Missense 9:107318848-107318848 + ESCC_BICR_002T COSM5440807 c.378C>A p.I126I Substitution - coding silent 9:107306528-107306528 + RMS2105 COSM5880976 c.1140_1141insAG p.G381fs*4 Insertion - Frameshift 9:107329566-107329567 + T1764 COSM4719951 c.558G>A p.T186T Substitution - coding silent 9:107318756-107318756 + TCGA-C5-A1BL-01 COSM4836899 c.448G>A p.E150K Substitution - Missense 9:107306598-107306598 + TCGA-BG-A0LX-01 COSM1103639 c.1148T>C p.V383A Substitution - Missense 9:107329574-107329574 + CHC205T COSM3763503 c.746C>T p.A249V Substitution - Missense 9:107322047-107322047 + 18 COSM5745051 c.542C>T p.T181M Substitution - Missense 9:107311726-107311726 + TCGA-AP-A059-01 COSM1103635 c.466C>T p.P156S Substitution - Missense 9:107306616-107306616 + AIMAH2 COSM5961791 c.937T>C p.L313L Substitution - coding silent 9:107324009-107324009 + sysucc-1317T COSM5450507 c.417T>C p.P139P Substitution - coding silent 9:107306567-107306567 + TCGA-AA-3672-01 COSM267305 c.629C>T p.A210V Substitution - Missense 9:107318827-107318827 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.521571;Hs.521575;Hs.521600;Hs.521603;Hs.521619;Hs.521623;Hs.521629;Hs.521636;Hs.521638;Hs.521640 9q31.2 600062

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer ACA - InFrameDeletion p.T269delT c.806_808delCAA 9 110084381 GBM A C Missense p.K36N c.108A>C 9 110062463 UCEC A G Synonymous p.A183A c.549A>G 9 110074014 HC A T IntronicSNV . c.1116+21A>T 9 110087306 BRCA C A Missense p.A124E c.371C>A 9 110068802 LUAD C A Missense p.T195N c.584C>A 9 110081063 CM C T Missense p.A386V c.1157C>T 9 110091864 COREAD C T Missense p.P275L c.824C>T 9 110086177 CM C T Missense p.P296L c.887C>T 9 110086240 CM C T Missense p.P40S c.118C>T 9 110062473 CM C T Missense p.S121F c.362C>T 9 110068793 CM C T Missense p.S297F c.890C>T 9 110086243 HNSC C T Missense p.T195I c.584C>T 9 110081063 OV C T Nonsense p.Q243* c.727C>T 9 110084309 GBM C T Nonsense p.Q293* c.877C>T 9 110086230 BRCA G A Missense p.R289K c.866G>A 9 110086219 BRCA G A Synonymous p.V383V c.1149G>A 9 110091856 HNSC GG - Frameshift p.A256Cfs*21 c.765_766delGG 9 110084347 RCCC G T Missense p.R372S c.1116G>T 9 110087285 LUAD T C Missense p.V383A c.1148T>C 9 110091855 UCEC T C Synonymous p.G169G c.507T>C 9 110073972 HNSC T - IntronicDeletion . c.554-23delT 9 110081004 STAD