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 127617983 127617983 + Silent SNP C C T TCGA-FJ-A3Z7-01A-12D-A23M-08 TCGA-FJ-A3Z7-10A-01D-A23K-08 g.chr9:127617983C>T c.261C>T c.(259-261)gtC>gtT p.V87V BLCA 9 127618143 127618146 + Frame_Shift_Del DEL ACCA ACCA - TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr9:127618143_127618146delACCA c.311_314delACCA c.(310-315)caccaafs p.HQ104fs BLCA 9 127618540 127618540 + Missense_Mutation SNP T T A TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr9:127618540T>A c.427T>A c.(427-429)Tta>Ata p.L143I BRCA 9 127619046 127619046 + Missense_Mutation SNP G G T TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr9:127619046G>T c.654G>T c.(652-654)tgG>tgT p.W218C BRCA 9 127619109 127619109 + Frame_Shift_Del DEL A A - TCGA-A8-A09X-01A-11W-A019-09 TCGA-A8-A09X-10A-01W-A021-09 g.chr9:127619109delA c.717delA c.(715-717)atafs p.I239fs BRCA 9 127619645 127619645 + Silent SNP C C G TCGA-C8-A3M8-01A-11D-A20S-09 TCGA-C8-A3M8-10A-01D-A20S-09 g.chr9:127619645C>G c.771C>G c.(769-771)gtC>gtG p.V257V CESC 9 127618159 127618159 + Silent SNP G G A TCGA-EA-A78R-01A-11D-A32I-09 TCGA-EA-A78R-10A-01D-A32I-09 g.chr9:127618159G>A c.327G>A c.(325-327)gaG>gaA p.E109E CESC 9 127619875 127619875 + Missense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr9:127619875G>A c.911G>A c.(910-912)cGc>cAc p.R304H COAD 9 127617985 127617985 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:127617985G>A c.263G>A c.(262-264)cGc>cAc p.R88H COAD 9 127618161 127618161 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:127618161C>T c.329C>T c.(328-330)aCg>aTg p.T110M COAD 9 127618524 127618524 + Silent SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:127618524C>T c.411C>T c.(409-411)ggC>ggT p.G137G COADREAD 9 127617985 127617985 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:127617985G>A c.263G>A c.(262-264)cGc>cAc p.R88H COADREAD 9 127618161 127618161 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:127618161C>T c.329C>T c.(328-330)aCg>aTg p.T110M COADREAD 9 127618524 127618524 + Silent SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:127618524C>T c.411C>T c.(409-411)ggC>ggT p.G137G DLBC 9 127618775 127618775 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr9:127618775C>T c.514C>T c.(514-516)Cac>Tac p.H172Y GBMLGG 9 127618017 127618017 + Missense_Mutation SNP C C T TCGA-P5-A737-01A-11D-A32B-08 TCGA-P5-A737-10A-01D-A329-08 g.chr9:127618017C>T c.295C>T c.(295-297)Cgg>Tgg p.R99W LGG 9 127618017 127618017 + Missense_Mutation SNP C C T TCGA-P5-A737-01A-11D-A32B-08 TCGA-P5-A737-10A-01D-A329-08 g.chr9:127618017C>T c.295C>T c.(295-297)Cgg>Tgg p.R99W LIHC 9 127619818 127619818 + Missense_Mutation SNP C C A TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr9:127619818C>A c.854C>A c.(853-855)cCa>cAa p.P285Q LIHC 9 127619833 127619834 + Frame_Shift_Ins INS - - A TCGA-DD-AADR-01A-11D-A40R-10 TCGA-DD-AADR-10A-01D-A40U-10 g.chr9:127619833_127619834insA c.869_870insA c.(868-873)ttagtgfs p.V291fs LIHC 9 127619900 127619900 + Silent SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr9:127619900T>C c.936T>C c.(934-936)ccT>ccC p.P312P LUAD 9 127618016 127618016 + Silent SNP G G A TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr9:127618016G>A c.294G>A c.(292-294)ctG>ctA p.L98L LUAD 9 127618838 127618838 + Missense_Mutation SNP G G A TCGA-75-5122-01A-01D-1753-08 TCGA-75-5122-10A-01D-1753-08 g.chr9:127618838G>A c.577G>A c.(577-579)Gcc>Acc p.A193T LUAD 9 127619095 127619095 + Missense_Mutation SNP T T A TCGA-05-5420-01A-01D-1625-08 TCGA-05-5420-11A-01D-1625-08 g.chr9:127619095T>A c.703T>A c.(703-705)Tgg>Agg p.W235R LUAD 9 127619792 127619792 + Missense_Mutation SNP T T A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr9:127619792T>A c.828T>A c.(826-828)gaT>gaA p.D276E LUAD 9 127619860 127619860 + Missense_Mutation SNP G G C TCGA-86-7711-01A-11D-2063-08 TCGA-86-7711-10A-01D-2063-08 g.chr9:127619860G>C c.896G>C c.(895-897)aGa>aCa p.R299T LUSC 9 127619793 127619793 + Missense_Mutation SNP G G A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr9:127619793G>A c.829G>A c.(829-831)Gtg>Atg p.V277M PRAD 9 127618187 127618187 + Missense_Mutation SNP C C A TCGA-CH-5744-01A-11D-1576-08 TCGA-CH-5744-10A-01D-1576-08 g.chr9:127618187C>A c.355C>A c.(355-357)Cag>Aag p.Q119K SKCM 9 127618151 127618151 + Missense_Mutation SNP A A C TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:127618151A>C c.319A>C c.(319-321)Agt>Cgt p.S107R SKCM 9 127618183 127618183 + Silent SNP G G A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr9:127618183G>A c.351G>A c.(349-351)tcG>tcA p.S117S SKCM 9 127618829 127618829 + Missense_Mutation SNP G G A TCGA-GN-A4U8-06A-11D-A32N-08 TCGA-GN-A4U8-10B-01D-A32N-08 g.chr9:127618829G>A c.568G>A c.(568-570)Gga>Aga p.G190R SKCM 9 127619030 127619030 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:127619030A>C c.638A>C c.(637-639)aAg>aCg p.K213T SKCM 9 127619824 127619824 + Missense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr9:127619824G>A c.860G>A c.(859-861)gGg>gAg p.G287E

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 127617983 127617983 single base substitution C T synonymous_variant V87V 261C>T BLCA-US 9 127623766 127623766 single base substitution C T downstream_gene_variant BOCA-FR 9 127619310 127619310 single base substitution G A intron_variant BRCA-EU 9 127611976 127611976 single base substitution C T upstream_gene_variant BRCA-EU 9 127613084 127613084 single base substitution C G upstream_gene_variant BRCA-EU 9 127613092 127613092 single base substitution A T upstream_gene_variant BRCA-EU 9 127614314 127614314 single base substitution G A upstream_gene_variant BRCA-EU 9 127614947 127614947 single base substitution T A upstream_gene_variant BRCA-EU 9 127615411 127615411 single base substitution G A upstream_gene_variant BRCA-EU 9 127616247 127616247 single base substitution T C intron_variant BRCA-EU 9 127618826 127618826 single base substitution G C missense_variant E189Q 565G>C BRCA-EU 9 127618933 127618933 single base substitution T A intron_variant BRCA-EU 9 127619270 127619270 single base substitution G A intron_variant BRCA-EU 9 127619986 127619986 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 127620191 127620191 single base substitution C T downstream_gene_variant BRCA-EU 9 127621613 127621613 single base substitution C G downstream_gene_variant BRCA-EU 9 127621850 127621850 single base substitution C T downstream_gene_variant BRCA-EU 9 127623169 127623170 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 9 127623256 127623256 single base substitution C T downstream_gene_variant BRCA-EU 9 127623287 127623287 single base substitution G C downstream_gene_variant BRCA-EU 9 127624226 127624226 single base substitution G A downstream_gene_variant BRCA-FR 9 127614314 127614314 single base substitution G A upstream_gene_variant BRCA-FR 9 127623287 127623287 single base substitution G C downstream_gene_variant BRCA-FR 9 127623289 127623289 single base substitution G C downstream_gene_variant BRCA-UK 9 127613383 127613383 single base substitution G C upstream_gene_variant BRCA-UK 9 127619820 127619820 single base substitution G A missense_variant D286N 856G>A BRCA-US 9 127619046 127619046 single base substitution G T missense_variant W218C 654G>T BRCA-US 9 127619109 127619109 deletion of <=200bp A - frameshift_variant I239 BRCA-US 9 127619645 127619645 single base substitution C G splice_region_variant BRCA-US 9 127620332 127620332 single base substitution C G downstream_gene_variant BTCA-JP 9 127617994 127617994 single base substitution A C missense_variant D91A 272A>C CESC-US 9 127618159 127618159 single base substitution G A synonymous_variant E109E 327G>A CESC-US 9 127619875 127619875 single base substitution G A missense_variant R304H 911G>A CESC-US 9 127622541 127622541 single base substitution C T downstream_gene_variant CESC-US 9 127623691 127623691 single base substitution C T downstream_gene_variant CLLE-ES 9 127610945 127610945 single base substitution T A upstream_gene_variant COAD-US 9 127618161 127618161 single base substitution C T missense_variant T110M 329C>T COAD-US 9 127620219 127620219 single base substitution C T downstream_gene_variant COAD-US 9 127623796 127623798 deletion of <=200bp CTT - downstream_gene_variant COCA-CN 9 127611679 127611679 single base substitution T C upstream_gene_variant COCA-CN 9 127611824 127611824 single base substitution T C upstream_gene_variant COCA-CN 9 127618148 127618148 single base substitution C T missense_variant R106W 316C>T COCA-CN 9 127619632 127619632 single base substitution T C intron_variant COCA-CN 9 127620653 127620653 single base substitution G A downstream_gene_variant COCA-CN 9 127622637 127622637 single base substitution C T downstream_gene_variant COCA-CN 9 127623946 127623946 single base substitution G A downstream_gene_variant ESAD-UK 9 127610953 127610953 single base substitution C G upstream_gene_variant ESAD-UK 9 127611107 127611107 single base substitution C G upstream_gene_variant ESAD-UK 9 127612041 127612041 single base substitution C A upstream_gene_variant ESAD-UK 9 127612223 127612223 single base substitution G T upstream_gene_variant ESAD-UK 9 127612717 127612717 single base substitution C T upstream_gene_variant ESAD-UK 9 127613207 127613207 single base substitution C T upstream_gene_variant ESAD-UK 9 127613244 127613244 single base substitution C G upstream_gene_variant ESAD-UK 9 127613264 127613264 single base substitution C T upstream_gene_variant ESAD-UK 9 127613498 127613498 single base substitution C T upstream_gene_variant ESAD-UK 9 127614492 127614492 single base substitution C G upstream_gene_variant ESAD-UK 9 127615482 127615482 single base substitution G C upstream_gene_variant ESAD-UK 9 127616455 127616455 single base substitution G A intron_variant ESAD-UK 9 127617415 127617415 single base substitution C T intron_variant ESAD-UK 9 127618831 127618832 deletion of <=200bp AC - frameshift_variant GH190 ESAD-UK 9 127619358 127619358 single base substitution T A intron_variant ESAD-UK 9 127620209 127620209 single base substitution C A downstream_gene_variant ESAD-UK 9 127620475 127620475 single base substitution C T downstream_gene_variant ESAD-UK 9 127622615 127622615 single base substitution G A downstream_gene_variant ESAD-UK 9 127622759 127622759 single base substitution G A downstream_gene_variant ESAD-UK 9 127623112 127623112 single base substitution G C downstream_gene_variant ESCA-CN 9 127616537 127616537 single base substitution A G synonymous_variant E41E 123A>G ESCA-CN 9 127619625 127619625 insertion of <=200bp - C intron_variant LAML-KR 9 127618776 127618776 single base substitution A G missense_variant H172R 515A>G LICA-FR 9 127619782 127619782 single base substitution G T missense_variant G273V 818G>T LICA-FR 9 127619783 127619783 single base substitution A T splice_region_variant LIHC-US 9 127622525 127622525 single base substitution G A downstream_gene_variant LINC-JP 9 127613597 127613597 single base substitution G T upstream_gene_variant LINC-JP 9 127613598 127613598 single base substitution T C upstream_gene_variant LINC-JP 9 127616812 127616812 single base substitution T C intron_variant LINC-JP 9 127624230 127624230 single base substitution G A downstream_gene_variant LINC-JP 9 127624393 127624393 single base substitution T G downstream_gene_variant LIRI-JP 9 127615265 127615265 single base substitution G A upstream_gene_variant LIRI-JP 9 127615995 127615995 single base substitution A G intron_variant LIRI-JP 9 127618790 127618790 single base substitution C T missense_variant R177W 529C>T LIRI-JP 9 127619195 127619195 single base substitution C A intron_variant LIRI-JP 9 127620299 127620299 single base substitution G A downstream_gene_variant LUSC-KR 9 127619662 127619662 single base substitution A C missense_variant N263T 788A>C LUSC-KR 9 127619726 127619726 single base substitution G C intron_variant LUSC-KR 9 127620141 127620141 single base substitution A G 3_prime_UTR_variant LUSC-US 9 127619793 127619793 single base substitution G A missense_variant V277M 829G>A MALY-DE 9 127619088 127619088 single base substitution T C synonymous_variant H232H 696T>C MALY-DE 9 127621181 127621181 single base substitution C A downstream_gene_variant MALY-DE 9 127622955 127622955 single base substitution G A downstream_gene_variant MELA-AU 9 127610827 127610827 single base substitution C T upstream_gene_variant MELA-AU 9 127611185 127611185 single base substitution C T upstream_gene_variant MELA-AU 9 127611272 127611272 single base substitution C T upstream_gene_variant MELA-AU 9 127612754 127612754 single base substitution C T upstream_gene_variant MELA-AU 9 127613376 127613376 single base substitution G A upstream_gene_variant MELA-AU 9 127613598 127613598 insertion of <=200bp - TTTT upstream_gene_variant MELA-AU 9 127613940 127613940 single base substitution G A upstream_gene_variant MELA-AU 9 127614129 127614129 single base substitution C T upstream_gene_variant MELA-AU 9 127614193 127614193 single base substitution G A upstream_gene_variant MELA-AU 9 127614231 127614231 single base substitution G A upstream_gene_variant MELA-AU 9 127614439 127614439 single base substitution G A upstream_gene_variant MELA-AU 9 127614446 127614446 single base substitution G A upstream_gene_variant MELA-AU 9 127616445 127616445 single base substitution T G intron_variant MELA-AU 9 127616887 127616887 single base substitution C T intron_variant MELA-AU 9 127618023 127618023 single base substitution C T synonymous_variant L101L 301C>T MELA-AU 9 127618440 127618440 single base substitution A G intron_variant MELA-AU 9 127618470 127618471 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 127618761 127618761 single base substitution G A stop_gained W167* 500G>A MELA-AU 9 127619440 127619440 single base substitution G A intron_variant MELA-AU 9 127622080 127622080 single base substitution G A downstream_gene_variant MELA-AU 9 127624230 127624230 single base substitution G A downstream_gene_variant MELA-AU 9 127624234 127624234 single base substitution G A downstream_gene_variant MELA-AU 9 127624308 127624308 single base substitution G A downstream_gene_variant MELA-AU 9 127624333 127624333 single base substitution C T downstream_gene_variant MELA-AU 9 127624440 127624440 single base substitution T A downstream_gene_variant ORCA-IN 9 127622836 127622836 single base substitution C T downstream_gene_variant OV-AU 9 127612845 127612845 single base substitution C G upstream_gene_variant OV-AU 9 127618391 127618391 single base substitution C T intron_variant OV-US 9 127620287 127620287 single base substitution C T downstream_gene_variant PACA-AU 9 127615825 127615825 single base substitution C T synonymous_variant V5V 15C>T PACA-AU 9 127620602 127620602 single base substitution G A downstream_gene_variant PACA-AU 9 127623549 127623549 single base substitution A G downstream_gene_variant PACA-AU 9 127624217 127624217 single base substitution G A downstream_gene_variant PACA-AU 9 127624668 127624668 single base substitution C G downstream_gene_variant PACA-CA 9 127612805 127612805 single base substitution T C upstream_gene_variant PACA-CA 9 127613618 127613618 single base substitution T C upstream_gene_variant PACA-CA 9 127615613 127615613 single base substitution C G upstream_gene_variant PACA-CA 9 127622724 127622724 single base substitution C A downstream_gene_variant PBCA-DE 9 127612266 127612266 single base substitution G A upstream_gene_variant PBCA-DE 9 127621038 127621038 single base substitution A G downstream_gene_variant PRAD-CA 9 127612068 127612068 single base substitution G A upstream_gene_variant PRAD-CA 9 127619875 127619875 single base substitution G C missense_variant R304P 911G>C PRAD-US 9 127618187 127618187 single base substitution C A missense_variant Q119K 355C>A READ-US 9 127620295 127620295 single base substitution G A downstream_gene_variant RECA-EU 9 127616418 127616418 single base substitution A T intron_variant RECA-EU 9 127620194 127620194 single base substitution C G downstream_gene_variant RECA-EU 9 127620196 127620196 single base substitution C A downstream_gene_variant SKCA-BR 9 127610873 127610873 single base substitution A T upstream_gene_variant SKCA-BR 9 127612909 127612909 single base substitution A C upstream_gene_variant SKCA-BR 9 127613109 127613109 insertion of <=200bp - GAA upstream_gene_variant SKCA-BR 9 127614834 127614834 single base substitution C T upstream_gene_variant SKCA-BR 9 127615577 127615577 single base substitution T C upstream_gene_variant SKCA-BR 9 127615669 127615669 single base substitution A G upstream_gene_variant SKCA-BR 9 127615881 127615881 single base substitution T G splice_donor_variant SKCA-BR 9 127619855 127619855 single base substitution G A synonymous_variant Q297Q 891G>A SKCA-BR 9 127624329 127624329 single base substitution C T downstream_gene_variant SKCA-BR 9 127624330 127624330 single base substitution T C downstream_gene_variant SKCM-US 9 127618183 127618183 single base substitution G A synonymous_variant S117S 351G>A SKCM-US 9 127619030 127619030 single base substitution A C missense_variant K213T 638A>C SKCM-US 9 127619777 127619777 single base substitution G A intron_variant SKCM-US 9 127619824 127619824 single base substitution G A missense_variant G287E 860G>A SKCM-US 9 127620225 127620225 single base substitution G A downstream_gene_variant STAD-US 9 127616484 127616484 single base substitution G C missense_variant V24L 70G>C STAD-US 9 127616498 127616498 single base substitution C A synonymous_variant A28A 84C>A STAD-US 9 127617935 127617935 single base substitution C A missense_variant F71L 213C>A STAD-US 9 127618544 127618544 single base substitution T C missense_variant V144A 431T>C STAD-US 9 127619662 127619662 single base substitution A G missense_variant N263S 788A>G STAD-US 9 127620344 127620344 single base substitution G A downstream_gene_variant UCEC-US 9 127616516 127616516 single base substitution G T missense_variant Q34H 102G>T UCEC-US 9 127616547 127616547 single base substitution G A missense_variant V45M 133G>A UCEC-US 9 127616566 127616566 single base substitution G A missense_variant R51Q 152G>A UCEC-US 9 127618189 127618189 single base substitution G T missense_variant Q119H 357G>T UCEC-US 9 127618537 127618538 deletion of <=200bp CT - frameshift_variant L142 UCEC-US 9 127618586 127618586 single base substitution C T missense_variant T158M 473C>T UCEC-US 9 127619016 127619016 single base substitution C T synonymous_variant S208S 624C>T UCEC-US 9 127619674 127619674 single base substitution G A missense_variant C267Y 800G>A UCEC-US 9 127620293 127620293 single base substitution G A downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PTC-7C COSM3982733 c.123A>G p.E41E Substitution - coding silent 9:124854258-124854258 + PT50 COSM5937411 c.725C>T p.S242F Substitution - Missense 9:124856838-124856838 + TCGA-A6-6653-01 COSM1459971 c.329C>T p.T110M Substitution - Missense 9:124855882-124855882 + RK279_C01 COSM3703477 c.529C>T p.R177W Substitution - Missense 9:124856511-124856511 + TCGA-FS-A1ZP-06 COSM3654300 c.351G>A p.S117S Substitution - coding silent 9:124855904-124855904 + CHC1775T COSM4800903 c.818G>T p.G273V Substitution - Missense 9:124857503-124857503 + J36_T COSM3952336 c.788A>C p.N263T Substitution - Missense 9:124857383-124857383 + TCGA-B5-A11Y-01 COSM1105097 c.152G>A p.R51Q Substitution - Missense 9:124854287-124854287 + TCGA-AP-A059-01 COSM1105100 c.473C>T p.T158M Substitution - Missense 9:124856307-124856307 + TCGA-22-4613-01 COSM752727 c.829G>A p.V277M Substitution - Missense 9:124857514-124857514 + 587336 COSM1232582 c.220G>A p.D74N Substitution - Missense 9:124855663-124855663 + pfg143T COSM4761146 c.886G>A p.D296N Substitution - Missense 9:124857571-124857571 + T3151 COSM4740953 c.47_48delTC p.F17fs*15 Deletion - Frameshift 9:124853578-124853579 + TCGA-CH-5744-01 COSM1132596 c.355C>A p.Q119K Substitution - Missense 9:124855908-124855908 + 2492722 COSM5721408 c.472A>C p.T158P Substitution - Missense 9:124856306-124856306 + TCGA-AP-A051-01 COSM1105102 c.800G>A p.C267Y Substitution - Missense 9:124857395-124857395 + TCGA-A8-A09X-01 COSM5835616 c.717delA p.I239fs*33 Deletion - Frameshift 9:124856830-124856830 + CN-AML-CR-41-Dx COSM5427083 c.515A>G p.H172R Substitution - Missense 9:124856497-124856497 + BD124T COSM5492580 c.272A>C p.D91A Substitution - Missense 9:124855715-124855715 + TCGA-AA-3977-01 COSM297642 c.263G>A p.R88H Substitution - Missense 9:124855706-124855706 + STC246 COSM5063599 c.511G>A p.V171I Substitution - Missense 9:124856493-124856493 + 1N53-VS-1T53 COSM4976951 c.618+1G>T p.? Unknown 9:124856601-124856601 + TCGA-B5-A11E-01 COSM1105101 c.624C>T p.S208S Substitution - coding silent 9:124856737-124856737 + CSCC-10-T COSM4503692 c.646C>T p.H216Y Substitution - Missense 9:124856759-124856759 + CHC1775T COSM4800946 c.819A>T p.G273G Substitution - coding silent 9:124857504-124857504 + TCGA-EA-A78R-01 COSM4852060 c.327G>A p.E109E Substitution - coding silent 9:124855880-124855880 + YUKAT COSM5410399 c.727C>T p.P243S Substitution - Missense 9:124856840-124856840 + TCGA-D3-A5GO-06 COSM3654302 c.860G>A p.G287E Substitution - Missense 9:124857545-124857545 + TCGA-AP-A0LT-01 COSM1105099 c.424_425delCT p.L143fs*5 Deletion - Frameshift 9:124856258-124856259 + TCGA-D1-A103-01 COSM1105095 c.102G>T p.Q34H Substitution - Missense 9:124854237-124854237 + CHEWS028 COSM1105097 c.152G>A p.R51Q Substitution - Missense 9:124854287-124854287 + TCGA-AP-A059-01 COSM1105098 c.357G>T p.Q119H Substitution - Missense 9:124855910-124855910 + TCGA-D9-A6EC-06 COSM4401737 c.638A>C p.K213T Substitution - Missense 9:124856751-124856751 + ZZUFHECRKL-G068T COSM3982733 c.123A>G p.E41E Substitution - coding silent 9:124854258-124854258 + 3402_T COSM3952335 c.646C>G p.H216D Substitution - Missense 9:124856759-124856759 + TCGA-EE-A2GL-06 COSM3654301 c.817-4G>A p.? Unknown 9:124857498-124857498 + 8066440 COSM3780644 c.15C>T p.V5V Substitution - coding silent 9:124853546-124853546 + 2492723 COSM5721408 c.472A>C p.T158P Substitution - Missense 9:124856306-124856306 + sysucc-1163T COSM5459399 c.316C>T p.R106W Substitution - Missense 9:124855869-124855869 + PD4137a COSM165566 c.856G>A p.D286N Substitution - Missense 9:124857541-124857541 + TCGA-A6-6780-01 COSM1459972 c.411C>T p.G137G Substitution - coding silent 9:124856245-124856245 + SNUH_G26_S1 COSM3982733 c.123A>G p.E41E Substitution - coding silent 9:124854258-124854258 + SNUH_G16_S1 COSM3982733 c.123A>G p.E41E Substitution - coding silent 9:124854258-124854258 + TCGA-D1-A103-01 COSM1105096 c.133G>A p.V45M Substitution - Missense 9:124854268-124854268 + TCGA-C8-A3M8-01 COSM3847639 c.771C>G p.V257V Substitution - coding silent 9:124857366-124857366 + TCGA-BR-4361-01 COSM3904043 c.431T>C p.V144A Substitution - Missense 9:124856265-124856265 + TCGA-CG-5726-01 COSM3904040 c.70G>C p.V24L Substitution - Missense 9:124854205-124854205 + HCT15 COSM1674829 c.144G>A p.W48* Substitution - Nonsense 9:124854279-124854279 + MO_1162 COSM5565215 c.764G>A p.R255H Substitution - Missense 9:124856877-124856877 + TCGA-FJ-A3Z7-01 COSM3779622 c.261C>T p.V87V Substitution - coding silent 9:124855704-124855704 + YUOMEGA COSM5410398 c.502G>T p.D168Y Substitution - Missense 9:124856484-124856484 + TCGA-D7-5579-01 COSM3904044 c.788A>G p.N263S Substitution - Missense 9:124857383-124857383 + CSCC-60-T COSM4506798 c.72C>A p.V24V Substitution - coding silent 9:124854207-124854207 + 2492729 COSM5727610 c.223G>A p.G75S Substitution - Missense 9:124855666-124855666 + HCT-15 COSM1674829 c.144G>A p.W48* Substitution - Nonsense 9:124854279-124854279 + Sample_1 COSM3982733 c.123A>G p.E41E Substitution - coding silent 9:124854258-124854258 + YULAD COSM5410400 c.799T>A p.C267S Substitution - Missense 9:124857394-124857394 + Pat_26_A COSM5875532 c.763C>T p.R255C Substitution - Missense 9:124856876-124856876 + tumor_4177376 COSM3358301 c.696T>C p.H232H Substitution - coding silent 9:124856809-124856809 + Au3 COSM5602603 c.733G>A p.E245K Substitution - Missense 9:124856846-124856846 + 2492721 COSM5721408 c.472A>C p.T158P Substitution - Missense 9:124856306-124856306 + 2492720 COSM5721408 c.472A>C p.T158P Substitution - Missense 9:124856306-124856306 + TCGA-CG-5723-01 COSM3904041 c.84C>A p.A28A Substitution - coding silent 9:124854219-124854219 + CHC1775T COSM4800903 c.818G>T p.G273V Substitution - Missense 9:124857503-124857503 + ME002T COSM222164 c.658_659CC>AA p.P220>? Complex 9:124856771-124856772 + CHC1775T COSM4800946 c.819A>T p.G273G Substitution - coding silent 9:124857504-124857504 + TCGA-C8-A3M7-01 COSM3847638 c.654G>T p.W218C Substitution - Missense 9:124856767-124856767 + TCGA-HU-A4GT-01 COSM3904042 c.213C>A p.F71L Substitution - Missense 9:124855656-124855656 + TCGA-CM-4743-01 COSM5156533 c.335G>A p.S112N Substitution - Missense 9:124855888-124855888 + CACO2 COSM3324730 c.257C>T p.T86I Substitution - Missense 9:124855700-124855700 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.343383 9q33.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.S107R c.319A>C 9 127618151 CM A G Missense p.N263S c.788A>G 9 127619662 STAD CC AA Missense p.P220N c.658_659delinsAA 9 127619050 CM CC TT 3-UTRBlockSubstitution . c.942+196_942+197delinsTT 9 127620102 CM CT - Frameshift p.L143Sfs*5 c.426_427delCT 9 127618537 UCEC G A Missense p.A193T c.577G>A 9 127618838 LUAD G A Missense p.D286N c.856G>A 9 127619820 BRCA G A Missense p.R51Q c.152G>A 9 127616566 UCEC G A Missense p.V277M c.829G>A 9 127619793 LUSC G A Synonymous p.S117S c.351G>A 9 127618183 CM G C Missense p.V24L c.70G>C 9 127616484 STAD T A Missense p.W235R c.703T>A 9 127619095 LUAD