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 140449838 140449838 + Silent SNP C C T TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr9:140449838C>T c.1212G>A c.(1210-1212)agG>agA p.R404R BLCA 9 140458893 140458893 + Missense_Mutation SNP C C G TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr9:140458893C>G c.942G>C c.(940-942)aaG>aaC p.K314N BLCA 9 140469295 140469295 + Splice_Site SNP T T C TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr9:140469295T>C c.376A>G c.(376-378)Aag>Gag p.K126E BLCA 9 140472024 140472024 + Missense_Mutation SNP C C A TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr9:140472024C>A c.185G>T c.(184-186)cGt>cTt p.R62L BLCA 9 140472031 140472031 + Nonsense_Mutation SNP G G A TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr9:140472031G>A c.178C>T c.(178-180)Cag>Tag p.Q60* BRCA 9 140449871 140449871 + Silent SNP C C T TCGA-D8-A1XJ-01A-11D-A14K-09 TCGA-D8-A1XJ-10A-01W-A16I-09 g.chr9:140449871C>T c.1179G>A c.(1177-1179)caG>caA p.Q393Q COAD 9 140458998 140458998 + Silent SNP C C T TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr9:140458998C>T c.837G>A c.(835-837)acG>acA p.T279T COAD 9 140459010 140459010 + Silent SNP C C T TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr9:140459010C>T c.825G>A c.(823-825)ccG>ccA p.P275P COADREAD 9 140458998 140458998 + Silent SNP C C T TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr9:140458998C>T c.837G>A c.(835-837)acG>acA p.T279T COADREAD 9 140459010 140459010 + Silent SNP C C T TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr9:140459010C>T c.825G>A c.(823-825)ccG>ccA p.P275P DLBC 9 140472034 140472034 + Missense_Mutation SNP G G C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr9:140472034G>C c.175C>G c.(175-177)Cct>Gct p.P59A GBMLGG 9 140459020 140459020 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140459020A>G c.815T>C c.(814-816)aTg>aCg p.M272T GBMLGG 9 140472007 140472007 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140472007G>T c.202C>A c.(202-204)Ctg>Atg p.L68M HNSC 9 140469251 140469251 + Silent SNP C C T TCGA-D6-A6EK-01A-11D-A31L-08 TCGA-D6-A6EK-10A-01D-A31J-08 g.chr9:140469251C>T c.420G>A c.(418-420)gaG>gaA p.E140E HNSC 9 140473185 140473185 + Silent SNP G G A TCGA-BA-4074-01A-01D-1434-08 TCGA-BA-4074-10A-01D-1434-08 g.chr9:140473185G>A c.45C>T c.(43-45)acC>acT p.T15T KIPAN 9 140449899 140449899 + Missense_Mutation SNP T T G TCGA-BP-4170-01A-02D-1366-10 TCGA-BP-4170-11A-01D-1366-10 g.chr9:140449899T>G c.1151A>C c.(1150-1152)aAc>aCc p.N384T KIRC 9 140449899 140449899 + Missense_Mutation SNP T T G TCGA-BP-4170-01A-02D-1366-10 TCGA-BP-4170-11A-01D-1366-10 g.chr9:140449899T>G c.1151A>C c.(1150-1152)aAc>aCc p.N384T LGG 9 140459020 140459020 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140459020A>G c.815T>C c.(814-816)aTg>aCg p.M272T LGG 9 140472007 140472007 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140472007G>T c.202C>A c.(202-204)Ctg>Atg p.L68M LUAD 9 140449977 140449977 + Missense_Mutation SNP C C A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr9:140449977C>A c.1073G>T c.(1072-1074)aGc>aTc p.S358I LUAD 9 140458994 140458994 + Missense_Mutation SNP C C A TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr9:140458994C>A c.841G>T c.(841-843)Gtg>Ttg p.V281L LUAD 9 140459346 140459346 + Splice_Site DEL T T - TCGA-75-5146-01A-01D-1625-08 TCGA-75-5146-10A-01D-1625-08 g.chr9:140459346delT c.775delA c.(775-777)agc>gc p.S259fs LUSC 9 140449841 140449841 + Missense_Mutation SNP C C T TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr9:140449841C>T c.1209G>A c.(1207-1209)atG>atA p.M403I LUSC 9 140468735 140468735 + Missense_Mutation SNP C C T TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr9:140468735C>T c.565G>A c.(565-567)Gcc>Acc p.A189T PRAD 9 140450002 140450002 + Missense_Mutation SNP G G A TCGA-HC-7232-01A-11D-2114-08 TCGA-HC-7232-10A-01D-2115-08 g.chr9:140450002G>A c.1048C>T c.(1048-1050)Cgg>Tgg p.R350W PRAD 9 140459546 140459546 + Missense_Mutation SNP G G C TCGA-G9-A9S0-01A-11D-A41K-08 TCGA-G9-A9S0-10A-01D-A41N-08 g.chr9:140459546G>C c.701C>G c.(700-702)aCc>aGc p.T234S PRAD 9 140468754 140468754 + Missense_Mutation SNP C C G TCGA-J4-A67L-01A-11D-A30E-08 TCGA-J4-A67L-10A-01D-A30H-08 g.chr9:140468754C>G c.546G>C c.(544-546)agG>agC p.R182S SKCM 9 140450030 140450030 + Nonsense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr9:140450030C>T c.1020G>A c.(1018-1020)tgG>tgA p.W340* SKCM 9 140450052 140450052 + Missense_Mutation SNP G G A TCGA-EE-A180-06A-11D-A21A-08 TCGA-EE-A180-10B-01D-A21A-08 g.chr9:140450052G>A c.998C>T c.(997-999)tCg>tTg p.S333L SKCM 9 140450068 140450068 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr9:140450068G>A c.982C>T c.(982-984)Cac>Tac p.H328Y SKCM 9 140458908 140458908 + Silent SNP G G A TCGA-D3-A1Q4-06A-11D-A196-08 TCGA-D3-A1Q4-10A-01D-A198-08 g.chr9:140458908G>A c.927C>T c.(925-927)atC>atT p.I309I SKCM 9 140459359 140459359 + Silent SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr9:140459359G>A c.762C>T c.(760-762)atC>atT p.I254I SKCM 9 140468793 140468793 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:140468793G>A c.507C>T c.(505-507)tcC>tcT p.S169S SKCM 9 140469207 140469207 + Missense_Mutation SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr9:140469207C>T c.464G>A c.(463-465)gGa>gAa p.G155E SKCM 9 140469211 140469211 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:140469211T>G c.460A>C c.(460-462)Act>Cct p.T154P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 9 140446860 140446860 single base substitution C T downstream_gene_variant BLCA-CN 9 140449708 140449708 single base substitution C G downstream_gene_variant BLCA-CN 9 140449708 140449708 single base substitution C G exon_variant BLCA-CN 9 140449708 140449708 single base substitution C G missense_variant E448Q 1342G>C BLCA-CN 9 140449918 140449918 single base substitution G A downstream_gene_variant BLCA-CN 9 140449918 140449918 single base substitution G A exon_variant BLCA-CN 9 140449918 140449918 single base substitution G A missense_variant H378Y 1132C>T BLCA-CN 9 140471927 140471927 single base substitution C T exon_variant BLCA-CN 9 140471927 140471927 single base substitution C T intron_variant BLCA-CN 9 140471927 140471927 single base substitution C T missense_variant M94I 282G>A BLCA-CN 9 140471927 140471927 single base substitution C T upstream_gene_variant BLCA-CN 9 140472055 140472055 single base substitution C A intron_variant BLCA-CN 9 140472055 140472055 single base substitution C A missense_variant G52C 154G>T BLCA-CN 9 140472055 140472055 single base substitution C A splice_region_variant BLCA-CN 9 140472055 140472055 single base substitution C A upstream_gene_variant BLCA-US 9 140444633 140444633 single base substitution T C downstream_gene_variant BLCA-US 9 140446562 140446562 single base substitution G A downstream_gene_variant BLCA-US 9 140446839 140446839 single base substitution G A downstream_gene_variant BLCA-US 9 140446923 140446923 single base substitution C T downstream_gene_variant BLCA-US 9 140477494 140477494 single base substitution C T upstream_gene_variant BRCA-EU 9 140444788 140444788 single base substitution G A downstream_gene_variant BRCA-EU 9 140447852 140447852 single base substitution A G downstream_gene_variant BRCA-EU 9 140449271 140449271 single base substitution G T downstream_gene_variant BRCA-EU 9 140451557 140451557 single base substitution C G intron_variant BRCA-EU 9 140451888 140451888 single base substitution G A intron_variant BRCA-EU 9 140452164 140452166 deletion of <=200bp AGG - intron_variant BRCA-EU 9 140453036 140453036 single base substitution A C intron_variant BRCA-EU 9 140453115 140453115 single base substitution G C intron_variant BRCA-EU 9 140453312 140453312 single base substitution A G intron_variant BRCA-EU 9 140454419 140454419 single base substitution C A downstream_gene_variant BRCA-EU 9 140454419 140454419 single base substitution C A intron_variant BRCA-EU 9 140454915 140454915 single base substitution G A downstream_gene_variant BRCA-EU 9 140454915 140454915 single base substitution G A intron_variant BRCA-EU 9 140454997 140454997 single base substitution C T downstream_gene_variant BRCA-EU 9 140454997 140454997 single base substitution C T intron_variant BRCA-EU 9 140455749 140455749 single base substitution A T downstream_gene_variant BRCA-EU 9 140455749 140455749 single base substitution A T intron_variant BRCA-EU 9 140464756 140464756 single base substitution T A downstream_gene_variant BRCA-EU 9 140464756 140464756 single base substitution T A intron_variant BRCA-EU 9 140464756 140464756 single base substitution T A upstream_gene_variant BRCA-EU 9 140471487 140471487 single base substitution C T intron_variant BRCA-EU 9 140471487 140471487 single base substitution C T upstream_gene_variant BRCA-EU 9 140472011 140472011 single base substitution G A exon_variant BRCA-EU 9 140472011 140472011 single base substitution G A intron_variant BRCA-EU 9 140472011 140472011 single base substitution G A synonymous_variant L66L 198C>T BRCA-EU 9 140472011 140472011 single base substitution G A upstream_gene_variant BRCA-EU 9 140472324 140472324 deletion of <=200bp C - intron_variant BRCA-EU 9 140472324 140472324 deletion of <=200bp C - upstream_gene_variant BRCA-EU 9 140472733 140472733 single base substitution C A intron_variant BRCA-EU 9 140472733 140472733 single base substitution C A upstream_gene_variant BRCA-EU 9 140473868 140473868 single base substitution C T upstream_gene_variant BRCA-EU 9 140475709 140475709 single base substitution G A upstream_gene_variant BRCA-EU 9 140476269 140476269 single base substitution G C upstream_gene_variant BRCA-EU 9 140477336 140477336 single base substitution C G upstream_gene_variant BRCA-FR 9 140473238 140473238 single base substitution C T 5_prime_UTR_variant BRCA-FR 9 140473238 140473238 single base substitution C T exon_variant BRCA-FR 9 140473238 140473238 single base substitution C T upstream_gene_variant BRCA-FR 9 140473868 140473868 single base substitution C T upstream_gene_variant BRCA-UK 9 140444806 140444806 single base substitution G T downstream_gene_variant BRCA-UK 9 140446656 140446656 single base substitution C T downstream_gene_variant BRCA-UK 9 140456502 140456502 single base substitution G C downstream_gene_variant BRCA-UK 9 140456502 140456502 single base substitution G C intron_variant BRCA-UK 9 140468798 140468798 single base substitution C T downstream_gene_variant BRCA-UK 9 140468798 140468798 single base substitution C T exon_variant BRCA-UK 9 140468798 140468798 single base substitution C T missense_variant D168N 502G>A BRCA-US 9 140449871 140449871 single base substitution C T downstream_gene_variant BRCA-US 9 140449871 140449871 single base substitution C T exon_variant BRCA-US 9 140449871 140449871 single base substitution C T synonymous_variant Q393Q 1179G>A BRCA-US 9 140477613 140477613 single base substitution T C upstream_gene_variant BTCA-JP 9 140446508 140446508 single base substitution C G downstream_gene_variant BTCA-JP 9 140450112 140450112 single base substitution G C downstream_gene_variant BTCA-JP 9 140450112 140450112 single base substitution G C intron_variant BTCA-JP 9 140451285 140451285 single base substitution A T intron_variant BTCA-JP 9 140459748 140459748 single base substitution C T exon_variant BTCA-JP 9 140459748 140459748 single base substitution C T intron_variant BTCA-JP 9 140459748 140459748 single base substitution C T upstream_gene_variant CESC-US 9 140446917 140446917 single base substitution C T downstream_gene_variant CESC-US 9 140451184 140451184 single base substitution C T exon_variant CESC-US 9 140451184 140451184 single base substitution C T intron_variant CESC-US 9 140459760 140459760 insertion of <=200bp - CT exon_variant CESC-US 9 140459760 140459760 insertion of <=200bp - CT intron_variant CESC-US 9 140459760 140459760 insertion of <=200bp - CT upstream_gene_variant CLLE-ES 9 140469356 140469356 single base substitution T A downstream_gene_variant CLLE-ES 9 140469356 140469356 single base substitution T A exon_variant CLLE-ES 9 140469356 140469356 single base substitution T A intron_variant COAD-US 9 140446782 140446782 single base substitution G A downstream_gene_variant COAD-US 9 140459010 140459010 single base substitution C T downstream_gene_variant COAD-US 9 140459010 140459010 single base substitution C T exon_variant COAD-US 9 140459010 140459010 single base substitution C T synonymous_variant P275P 825G>A COAD-US 9 140459370 140459370 single base substitution G A downstream_gene_variant COAD-US 9 140459370 140459370 single base substitution G A exon_variant COAD-US 9 140459370 140459370 single base substitution G A intron_variant COAD-US 9 140459370 140459370 single base substitution G A missense_variant R251W 751C>T COAD-US 9 140473154 140473154 single base substitution C A exon_variant COAD-US 9 140473154 140473154 single base substitution C A missense_variant G26C 76G>T COAD-US 9 140473154 140473154 single base substitution C A upstream_gene_variant COCA-CN 9 140446828 140446828 single base substitution G A downstream_gene_variant COCA-CN 9 140453664 140453664 single base substitution C A intron_variant COCA-CN 9 140453682 140453682 single base substitution G T intron_variant COCA-CN 9 140453722 140453722 single base substitution T C intron_variant COCA-CN 9 140453794 140453794 single base substitution G A intron_variant COCA-CN 9 140453808 140453808 single base substitution C T intron_variant COCA-CN 9 140453814 140453814 single base substitution C T intron_variant COCA-CN 9 140453824 140453824 single base substitution G C intron_variant COCA-CN 9 140459724 140459724 single base substitution G T exon_variant COCA-CN 9 140459724 140459724 single base substitution G T intron_variant COCA-CN 9 140459724 140459724 single base substitution G T upstream_gene_variant COCA-CN 9 140471806 140471806 single base substitution G T intron_variant COCA-CN 9 140471806 140471806 single base substitution G T upstream_gene_variant EOPC-DE 9 140458999 140458999 single base substitution G A downstream_gene_variant EOPC-DE 9 140458999 140458999 single base substitution G A exon_variant EOPC-DE 9 140458999 140458999 single base substitution G A missense_variant T279M 836C>T ESAD-UK 9 140447019 140447019 insertion of <=200bp - T downstream_gene_variant ESAD-UK 9 140449721 140449721 insertion of <=200bp - C downstream_gene_variant ESAD-UK 9 140449721 140449721 insertion of <=200bp - C exon_variant ESAD-UK 9 140449721 140449721 insertion of <=200bp - C frameshift_variant A443A? ESAD-UK 9 140450890 140450890 single base substitution C T downstream_gene_variant ESAD-UK 9 140450890 140450890 single base substitution C T intron_variant ESAD-UK 9 140455416 140455416 single base substitution G T downstream_gene_variant ESAD-UK 9 140455416 140455416 single base substitution G T intron_variant ESAD-UK 9 140455785 140455785 deletion of <=200bp A - downstream_gene_variant ESAD-UK 9 140455785 140455785 deletion of <=200bp A - intron_variant ESAD-UK 9 140456064 140456064 single base substitution G A downstream_gene_variant ESAD-UK 9 140456064 140456064 single base substitution G A intron_variant ESAD-UK 9 140458215 140458215 single base substitution A G downstream_gene_variant ESAD-UK 9 140458215 140458215 single base substitution A G intron_variant ESAD-UK 9 140463140 140463140 single base substitution C T intron_variant ESAD-UK 9 140463140 140463140 single base substitution C T upstream_gene_variant ESAD-UK 9 140463655 140463655 single base substitution C T intron_variant ESAD-UK 9 140463655 140463655 single base substitution C T upstream_gene_variant ESAD-UK 9 140467280 140467280 single base substitution A C downstream_gene_variant ESAD-UK 9 140467280 140467280 single base substitution A C intron_variant ESAD-UK 9 140468862 140468862 single base substitution G A downstream_gene_variant ESAD-UK 9 140468862 140468862 single base substitution G A exon_variant ESAD-UK 9 140468862 140468862 single base substitution G A intron_variant ESAD-UK 9 140470098 140470098 single base substitution A T exon_variant ESAD-UK 9 140470098 140470098 single base substitution A T intron_variant ESAD-UK 9 140470098 140470098 single base substitution A T upstream_gene_variant ESAD-UK 9 140471290 140471290 single base substitution C T intron_variant ESAD-UK 9 140471290 140471290 single base substitution C T upstream_gene_variant ESAD-UK 9 140472512 140472512 single base substitution G A intron_variant ESAD-UK 9 140472512 140472512 single base substitution G A upstream_gene_variant ESAD-UK 9 140473388 140473388 single base substitution T C upstream_gene_variant ESAD-UK 9 140473919 140473919 single base substitution G A upstream_gene_variant ESAD-UK 9 140474344 140474344 single base substitution G A upstream_gene_variant ESAD-UK 9 140475438 140475438 single base substitution C T upstream_gene_variant ESAD-UK 9 140475443 140475443 single base substitution C G upstream_gene_variant ESAD-UK 9 140476719 140476719 single base substitution T C upstream_gene_variant ESAD-UK 9 140476727 140476727 deletion of <=200bp A - upstream_gene_variant ESCA-CN 9 140450068 140450068 single base substitution G A downstream_gene_variant ESCA-CN 9 140450068 140450068 single base substitution G A exon_variant ESCA-CN 9 140450068 140450068 single base substitution G A missense_variant H328Y 982C>T ESCA-CN 9 140471966 140471966 single base substitution G C exon_variant ESCA-CN 9 140471966 140471966 single base substitution G C intron_variant ESCA-CN 9 140471966 140471966 single base substitution G C synonymous_variant V81V 243C>G ESCA-CN 9 140471966 140471966 single base substitution G C upstream_gene_variant GBM-US 9 140477434 140477434 single base substitution C T upstream_gene_variant KIRC-US 9 140449899 140449899 single base substitution T G downstream_gene_variant KIRC-US 9 140449899 140449899 single base substitution T G exon_variant KIRC-US 9 140449899 140449899 single base substitution T G missense_variant N384T 1151A>C LAML-KR 9 140452334 140452334 single base substitution C T intron_variant LAML-KR 9 140452336 140452336 single base substitution T C intron_variant LAML-KR 9 140459696 140459696 single base substitution G T exon_variant LAML-KR 9 140459696 140459696 single base substitution G T intron_variant LAML-KR 9 140459696 140459696 single base substitution G T upstream_gene_variant LAML-KR 9 140463028 140463028 single base substitution G T intron_variant LAML-KR 9 140463028 140463028 single base substitution G T upstream_gene_variant LAML-KR 9 140464304 140464304 single base substitution A C downstream_gene_variant LAML-KR 9 140464304 140464304 single base substitution A C intron_variant LAML-KR 9 140464304 140464304 single base substitution A C upstream_gene_variant LAML-KR 9 140464441 140464441 single base substitution C T downstream_gene_variant LAML-KR 9 140464441 140464441 single base substitution C T intron_variant LAML-KR 9 140464441 140464441 single base substitution C T upstream_gene_variant LAML-KR 9 140477249 140477249 single base substitution G A upstream_gene_variant LGG-US 9 140446796 140446796 deletion of <=200bp C - downstream_gene_variant LICA-FR 9 140458971 140458971 single base substitution G A downstream_gene_variant LICA-FR 9 140458971 140458971 single base substitution G A exon_variant LICA-FR 9 140458971 140458971 single base substitution G A synonymous_variant I288I 864C>T LICA-FR 9 140473177 140473177 single base substitution G T exon_variant LICA-FR 9 140473177 140473177 single base substitution G T stop_gained S18* 53C>A LICA-FR 9 140473177 140473177 single base substitution G T upstream_gene_variant LINC-JP 9 140445654 140445654 single base substitution C G downstream_gene_variant LINC-JP 9 140477070 140477072 deletion of <=200bp CTT - upstream_gene_variant LIRI-JP 9 140444811 140444811 single base substitution T C downstream_gene_variant LIRI-JP 9 140449883 140449883 single base substitution A G downstream_gene_variant LIRI-JP 9 140449883 140449883 single base substitution A G exon_variant LIRI-JP 9 140449883 140449883 single base substitution A G synonymous_variant H389H 1167T>C LIRI-JP 9 140451135 140451135 single base substitution C T exon_variant LIRI-JP 9 140451135 140451135 single base substitution C T intron_variant LIRI-JP 9 140478184 140478184 single base substitution A T upstream_gene_variant LUSC-KR 9 140444991 140444991 single base substitution C T downstream_gene_variant LUSC-KR 9 140446606 140446606 single base substitution C A downstream_gene_variant LUSC-KR 9 140447531 140447531 single base substitution G A downstream_gene_variant LUSC-KR 9 140455494 140455494 single base substitution G A downstream_gene_variant LUSC-KR 9 140455494 140455494 single base substitution G A intron_variant LUSC-KR 9 140460046 140460046 single base substitution T G intron_variant LUSC-KR 9 140460046 140460046 single base substitution T G upstream_gene_variant LUSC-KR 9 140462558 140462558 single base substitution T G intron_variant LUSC-KR 9 140462558 140462558 single base substitution T G upstream_gene_variant LUSC-KR 9 140462572 140462572 single base substitution T C intron_variant LUSC-KR 9 140462572 140462572 single base substitution T C upstream_gene_variant LUSC-KR 9 140462618 140462618 single base substitution T G intron_variant LUSC-KR 9 140462618 140462618 single base substitution T G upstream_gene_variant LUSC-KR 9 140463028 140463028 single base substitution G T intron_variant LUSC-KR 9 140463028 140463028 single base substitution G T upstream_gene_variant LUSC-KR 9 140471696 140471696 single base substitution C A intron_variant LUSC-KR 9 140471696 140471696 single base substitution C A upstream_gene_variant LUSC-KR 9 140477657 140477657 single base substitution C T upstream_gene_variant LUSC-US 9 140446840 140446840 single base substitution G T downstream_gene_variant LUSC-US 9 140449841 140449841 single base substitution C T downstream_gene_variant LUSC-US 9 140449841 140449841 single base substitution C T exon_variant LUSC-US 9 140449841 140449841 single base substitution C T missense_variant M403I 1209G>A LUSC-US 9 140468735 140468735 single base substitution C T downstream_gene_variant LUSC-US 9 140468735 140468735 single base substitution C T exon_variant LUSC-US 9 140468735 140468735 single base substitution C T missense_variant A189T 565G>A MALY-DE 9 140450755 140450755 single base substitution G A downstream_gene_variant MALY-DE 9 140450755 140450755 single base substitution G A intron_variant MALY-DE 9 140451102 140451102 single base substitution G A exon_variant MALY-DE 9 140451102 140451102 single base substitution G A intron_variant MELA-AU 9 140445878 140445878 single base substitution G T downstream_gene_variant MELA-AU 9 140446355 140446355 single base substitution G A downstream_gene_variant MELA-AU 9 140447137 140447137 single base substitution C T downstream_gene_variant MELA-AU 9 140449060 140449060 single base substitution T C downstream_gene_variant MELA-AU 9 140450426 140450426 single base substitution G A downstream_gene_variant MELA-AU 9 140450426 140450426 single base substitution G A intron_variant MELA-AU 9 140451320 140451320 single base substitution G A intron_variant MELA-AU 9 140451851 140451851 single base substitution G A intron_variant MELA-AU 9 140452055 140452055 single base substitution G A intron_variant MELA-AU 9 140452740 140452741 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 140453215 140453215 single base substitution A T intron_variant MELA-AU 9 140453874 140453874 single base substitution C T intron_variant MELA-AU 9 140456094 140456094 single base substitution G A downstream_gene_variant MELA-AU 9 140456094 140456094 single base substitution G A intron_variant MELA-AU 9 140456206 140456206 single base substitution G A downstream_gene_variant MELA-AU 9 140456206 140456206 single base substitution G A intron_variant MELA-AU 9 140456829 140456829 single base substitution G A downstream_gene_variant MELA-AU 9 140456829 140456829 single base substitution G A intron_variant MELA-AU 9 140457614 140457614 single base substitution G A downstream_gene_variant MELA-AU 9 140457614 140457614 single base substitution G A intron_variant MELA-AU 9 140458075 140458075 single base substitution G A downstream_gene_variant MELA-AU 9 140458075 140458075 single base substitution G A intron_variant MELA-AU 9 140458660 140458660 single base substitution G A downstream_gene_variant MELA-AU 9 140458660 140458660 single base substitution G A intron_variant MELA-AU 9 140459127 140459128 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 140459127 140459128 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 9 140459127 140459128 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 140459230 140459230 single base substitution G A downstream_gene_variant MELA-AU 9 140459230 140459230 single base substitution G A exon_variant MELA-AU 9 140459230 140459230 single base substitution G A intron_variant MELA-AU 9 140459251 140459251 single base substitution G A downstream_gene_variant MELA-AU 9 140459251 140459251 single base substitution G A exon_variant MELA-AU 9 140459251 140459251 single base substitution G A intron_variant MELA-AU 9 140459270 140459270 single base substitution G A downstream_gene_variant MELA-AU 9 140459270 140459270 single base substitution G A exon_variant MELA-AU 9 140459270 140459270 single base substitution G A intron_variant MELA-AU 9 140459310 140459310 single base substitution G A downstream_gene_variant MELA-AU 9 140459310 140459310 single base substitution G A exon_variant MELA-AU 9 140459310 140459310 single base substitution G A intron_variant MELA-AU 9 140459432 140459432 single base substitution G A downstream_gene_variant MELA-AU 9 140459432 140459432 single base substitution G A exon_variant MELA-AU 9 140459432 140459432 single base substitution G A intron_variant MELA-AU 9 140463213 140463213 single base substitution G A intron_variant MELA-AU 9 140463213 140463213 single base substitution G A upstream_gene_variant MELA-AU 9 140463217 140463217 single base substitution G A intron_variant MELA-AU 9 140463217 140463217 single base substitution G A upstream_gene_variant MELA-AU 9 140463476 140463476 single base substitution G A intron_variant MELA-AU 9 140463476 140463476 single base substitution G A upstream_gene_variant MELA-AU 9 140464421 140464421 single base substitution C T downstream_gene_variant MELA-AU 9 140464421 140464421 single base substitution C T intron_variant MELA-AU 9 140464421 140464421 single base substitution C T upstream_gene_variant MELA-AU 9 140464531 140464531 single base substitution C T downstream_gene_variant MELA-AU 9 140464531 140464531 single base substitution C T intron_variant MELA-AU 9 140464531 140464531 single base substitution C T upstream_gene_variant MELA-AU 9 140464696 140464696 single base substitution G A downstream_gene_variant MELA-AU 9 140464696 140464696 single base substitution G A intron_variant MELA-AU 9 140464696 140464696 single base substitution G A upstream_gene_variant MELA-AU 9 140467100 140467100 single base substitution C T downstream_gene_variant MELA-AU 9 140467100 140467100 single base substitution C T intron_variant MELA-AU 9 140467528 140467528 single base substitution A G downstream_gene_variant MELA-AU 9 140467528 140467528 single base substitution A G intron_variant MELA-AU 9 140468007 140468007 single base substitution T A downstream_gene_variant MELA-AU 9 140468007 140468007 single base substitution T A intron_variant MELA-AU 9 140468054 140468054 single base substitution G A downstream_gene_variant MELA-AU 9 140468054 140468054 single base substitution G A intron_variant MELA-AU 9 140469328 140469329 multiple base substitution (>=2bp and <=200bp) AG GA downstream_gene_variant MELA-AU 9 140469328 140469329 multiple base substitution (>=2bp and <=200bp) AG GA exon_variant MELA-AU 9 140469328 140469329 multiple base substitution (>=2bp and <=200bp) AG GA intron_variant MELA-AU 9 140470057 140470057 single base substitution G A exon_variant MELA-AU 9 140470057 140470057 single base substitution G A intron_variant MELA-AU 9 140470057 140470057 single base substitution G A upstream_gene_variant MELA-AU 9 140470726 140470726 single base substitution C T intron_variant MELA-AU 9 140470726 140470726 single base substitution C T upstream_gene_variant MELA-AU 9 140471236 140471236 single base substitution G A intron_variant MELA-AU 9 140471236 140471236 single base substitution G A upstream_gene_variant MELA-AU 9 140472106 140472106 single base substitution C T intron_variant MELA-AU 9 140472106 140472106 single base substitution C T upstream_gene_variant MELA-AU 9 140472216 140472216 single base substitution T C intron_variant MELA-AU 9 140472216 140472216 single base substitution T C upstream_gene_variant MELA-AU 9 140472658 140472658 single base substitution C T intron_variant MELA-AU 9 140472658 140472658 single base substitution C T upstream_gene_variant MELA-AU 9 140473378 140473378 single base substitution C T 5_prime_UTR_variant MELA-AU 9 140473378 140473378 single base substitution C T upstream_gene_variant MELA-AU 9 140473379 140473379 single base substitution C T 5_prime_UTR_variant MELA-AU 9 140473379 140473379 single base substitution C T upstream_gene_variant MELA-AU 9 140473382 140473383 multiple base substitution (>=2bp and <=200bp) CC TT 5_prime_UTR_variant MELA-AU 9 140473382 140473383 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 140473385 140473385 single base substitution G A 5_prime_UTR_variant MELA-AU 9 140473385 140473385 single base substitution G A upstream_gene_variant MELA-AU 9 140474208 140474208 single base substitution A G upstream_gene_variant MELA-AU 9 140475350 140475350 single base substitution T C upstream_gene_variant MELA-AU 9 140475669 140475669 single base substitution G A upstream_gene_variant MELA-AU 9 140476612 140476612 single base substitution G A upstream_gene_variant MELA-AU 9 140476613 140476613 single base substitution G T upstream_gene_variant NBL-US 9 140472047 140472047 single base substitution C A exon_variant NBL-US 9 140472047 140472047 single base substitution C A intron_variant NBL-US 9 140472047 140472047 single base substitution C A missense_variant M54I 162G>T NBL-US 9 140472047 140472047 single base substitution C A upstream_gene_variant ORCA-IN 9 140449992 140449992 single base substitution G A downstream_gene_variant ORCA-IN 9 140449992 140449992 single base substitution G A exon_variant ORCA-IN 9 140449992 140449992 single base substitution G A missense_variant S353L 1058C>T ORCA-IN 9 140471694 140471694 single base substitution G A intron_variant ORCA-IN 9 140471694 140471694 single base substitution G A upstream_gene_variant ORCA-IN 9 140474114 140474114 deletion of <=200bp G - upstream_gene_variant OV-AU 9 140449894 140449894 single base substitution C G downstream_gene_variant OV-AU 9 140449894 140449894 single base substitution C G exon_variant OV-AU 9 140449894 140449894 single base substitution C G missense_variant G386R 1156G>C OV-AU 9 140455784 140455784 single base substitution C T downstream_gene_variant OV-AU 9 140455784 140455784 single base substitution C T intron_variant OV-AU 9 140463359 140463359 single base substitution C A intron_variant OV-AU 9 140463359 140463359 single base substitution C A upstream_gene_variant OV-AU 9 140468453 140468453 single base substitution G A downstream_gene_variant OV-AU 9 140468453 140468453 single base substitution G A intron_variant OV-AU 9 140470333 140470333 single base substitution T C exon_variant OV-AU 9 140470333 140470333 single base substitution T C intron_variant OV-AU 9 140470333 140470333 single base substitution T C upstream_gene_variant OV-AU 9 140474161 140474161 single base substitution T G upstream_gene_variant OV-AU 9 140475118 140475118 single base substitution C T upstream_gene_variant OV-AU 9 140475878 140475878 single base substitution C A upstream_gene_variant PACA-AU 9 140448842 140448842 single base substitution C T downstream_gene_variant PACA-AU 9 140452437 140452437 single base substitution A T intron_variant PACA-AU 9 140453399 140453399 single base substitution C T intron_variant PACA-AU 9 140455490 140455490 single base substitution A G downstream_gene_variant PACA-AU 9 140455490 140455490 single base substitution A G intron_variant PACA-AU 9 140470613 140470613 single base substitution G A exon_variant PACA-AU 9 140470613 140470613 single base substitution G A synonymous_variant H98H 294C>T PACA-AU 9 140470613 140470613 single base substitution G A upstream_gene_variant PACA-AU 9 140473999 140473999 single base substitution C T upstream_gene_variant PACA-CA 9 140452378 140452378 single base substitution G A intron_variant PACA-CA 9 140452851 140452851 single base substitution T A intron_variant PACA-CA 9 140452899 140452899 deletion of <=200bp A - intron_variant PACA-CA 9 140463308 140463308 single base substitution T G intron_variant PACA-CA 9 140463308 140463308 single base substitution T G upstream_gene_variant PACA-CA 9 140465566 140465566 single base substitution C T downstream_gene_variant PACA-CA 9 140465566 140465566 single base substitution C T intron_variant PACA-CA 9 140465945 140465945 insertion of <=200bp - GG downstream_gene_variant PACA-CA 9 140465945 140465945 insertion of <=200bp - GG intron_variant PACA-CA 9 140465955 140465958 deletion of <=200bp AAGA - downstream_gene_variant PACA-CA 9 140465955 140465958 deletion of <=200bp AAGA - intron_variant PACA-CA 9 140467006 140467006 single base substitution C T downstream_gene_variant PACA-CA 9 140467006 140467006 single base substitution C T intron_variant PACA-CA 9 140469028 140469028 single base substitution T G downstream_gene_variant PACA-CA 9 140469028 140469028 single base substitution T G exon_variant PACA-CA 9 140469028 140469028 single base substitution T G intron_variant PACA-CA 9 140469751 140469751 single base substitution G A downstream_gene_variant PACA-CA 9 140469751 140469751 single base substitution G A exon_variant PACA-CA 9 140469751 140469751 single base substitution G A intron_variant PACA-CA 9 140469751 140469751 single base substitution G A upstream_gene_variant PACA-CA 9 140475129 140475129 single base substitution G A upstream_gene_variant PACA-CA 9 140476190 140476190 single base substitution C T upstream_gene_variant PACA-CA 9 140477944 140477944 single base substitution A G upstream_gene_variant PAEN-AU 9 140463075 140463075 single base substitution G C intron_variant PAEN-AU 9 140463075 140463075 single base substitution G C upstream_gene_variant PAEN-AU 9 140470189 140470189 single base substitution C G exon_variant PAEN-AU 9 140470189 140470189 single base substitution C G intron_variant PAEN-AU 9 140470189 140470189 single base substitution C G upstream_gene_variant PAEN-IT 9 140448653 140448653 single base substitution G T downstream_gene_variant PAEN-IT 9 140469855 140469855 single base substitution T C downstream_gene_variant PAEN-IT 9 140469855 140469855 single base substitution T C intron_variant PAEN-IT 9 140469855 140469855 single base substitution T C upstream_gene_variant PBCA-DE 9 140445648 140445648 single base substitution G T downstream_gene_variant PBCA-DE 9 140446186 140446186 single base substitution A G downstream_gene_variant PBCA-DE 9 140473789 140473789 single base substitution C T upstream_gene_variant PRAD-CA 9 140455826 140455826 single base substitution C T downstream_gene_variant PRAD-CA 9 140455826 140455826 single base substitution C T intron_variant PRAD-CA 9 140473632 140473632 single base substitution G C upstream_gene_variant PRAD-CA 9 140474294 140474294 single base substitution G C upstream_gene_variant PRAD-UK 9 140450757 140450757 single base substitution G A downstream_gene_variant PRAD-UK 9 140450757 140450757 single base substitution G A intron_variant PRAD-UK 9 140455222 140455222 single base substitution G A downstream_gene_variant PRAD-UK 9 140455222 140455222 single base substitution G A intron_variant PRAD-UK 9 140474512 140474512 single base substitution G C upstream_gene_variant PRAD-US 9 140450002 140450002 single base substitution G A downstream_gene_variant PRAD-US 9 140450002 140450002 single base substitution G A exon_variant PRAD-US 9 140450002 140450002 single base substitution G A missense_variant R350W 1048C>T PRAD-US 9 140468754 140468754 single base substitution C G downstream_gene_variant PRAD-US 9 140468754 140468754 single base substitution C G exon_variant PRAD-US 9 140468754 140468754 single base substitution C G missense_variant R182S 546G>C RECA-EU 9 140455473 140455473 single base substitution C A downstream_gene_variant RECA-EU 9 140455473 140455473 single base substitution C A intron_variant RECA-EU 9 140455486 140455486 single base substitution A G downstream_gene_variant RECA-EU 9 140455486 140455486 single base substitution A G intron_variant SKCA-BR 9 140448148 140448148 single base substitution T G downstream_gene_variant SKCA-BR 9 140448369 140448369 insertion of <=200bp - CAA downstream_gene_variant SKCA-BR 9 140453459 140453459 single base substitution G A intron_variant SKCA-BR 9 140455307 140455308 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 9 140455307 140455308 deletion of <=200bp CA - intron_variant SKCA-BR 9 140455486 140455486 insertion of <=200bp - AAAAAAAG downstream_gene_variant SKCA-BR 9 140455486 140455486 insertion of <=200bp - AAAAAAAG intron_variant SKCA-BR 9 140462618 140462618 single base substitution T G intron_variant SKCA-BR 9 140462618 140462618 single base substitution T G upstream_gene_variant SKCA-BR 9 140462762 140462762 single base substitution T G intron_variant SKCA-BR 9 140462762 140462762 single base substitution T G upstream_gene_variant SKCA-BR 9 140464369 140464369 single base substitution T C downstream_gene_variant SKCA-BR 9 140464369 140464369 single base substitution T C intron_variant SKCA-BR 9 140464369 140464369 single base substitution T C upstream_gene_variant SKCA-BR 9 140464748 140464748 single base substitution C T downstream_gene_variant SKCA-BR 9 140464748 140464748 single base substitution C T intron_variant SKCA-BR 9 140464748 140464748 single base substitution C T upstream_gene_variant SKCA-BR 9 140471117 140471117 single base substitution T G intron_variant SKCA-BR 9 140471117 140471117 single base substitution T G upstream_gene_variant SKCA-BR 9 140471505 140471505 insertion of <=200bp - CAAAAAA intron_variant SKCA-BR 9 140471505 140471505 insertion of <=200bp - CAAAAAA upstream_gene_variant SKCA-BR 9 140473084 140473084 single base substitution T G exon_variant SKCA-BR 9 140473084 140473084 single base substitution T G missense_variant Q49P 146A>C SKCA-BR 9 140473084 140473084 single base substitution T G upstream_gene_variant SKCA-BR 9 140473422 140473422 single base substitution C T upstream_gene_variant SKCA-BR 9 140476053 140476053 single base substitution G A upstream_gene_variant SKCA-BR 9 140476317 140476317 single base substitution T C upstream_gene_variant SKCA-BR 9 140478086 140478086 insertion of <=200bp - TGCTGTACAGAACAGGCCCTGGAGCGA upstream_gene_variant SKCM-US 9 140446713 140446713 single base substitution C T downstream_gene_variant SKCM-US 9 140446788 140446788 single base substitution C T downstream_gene_variant SKCM-US 9 140450030 140450030 single base substitution C T downstream_gene_variant SKCM-US 9 140450030 140450030 single base substitution C T exon_variant SKCM-US 9 140450030 140450030 single base substitution C T stop_gained W340* 1020G>A SKCM-US 9 140450052 140450052 single base substitution G A downstream_gene_variant SKCM-US 9 140450052 140450052 single base substitution G A exon_variant SKCM-US 9 140450052 140450052 single base substitution G A missense_variant S333L 998C>T SKCM-US 9 140450068 140450068 single base substitution G A downstream_gene_variant SKCM-US 9 140450068 140450068 single base substitution G A exon_variant SKCM-US 9 140450068 140450068 single base substitution G A missense_variant H328Y 982C>T SKCM-US 9 140458908 140458908 single base substitution G A downstream_gene_variant SKCM-US 9 140458908 140458908 single base substitution G A exon_variant SKCM-US 9 140458908 140458908 single base substitution G A synonymous_variant I309I 927C>T SKCM-US 9 140468793 140468793 single base substitution G A downstream_gene_variant SKCM-US 9 140468793 140468793 single base substitution G A exon_variant SKCM-US 9 140468793 140468793 single base substitution G A synonymous_variant S169S 507C>T SKCM-US 9 140469207 140469207 single base substitution C T downstream_gene_variant SKCM-US 9 140469207 140469207 single base substitution C T exon_variant SKCM-US 9 140469207 140469207 single base substitution C T missense_variant G155E 464G>A SKCM-US 9 140469211 140469211 single base substitution T G downstream_gene_variant SKCM-US 9 140469211 140469211 single base substitution T G exon_variant SKCM-US 9 140469211 140469211 single base substitution T G missense_variant T154P 460A>C STAD-US 9 140446797 140446797 single base substitution C T downstream_gene_variant STAD-US 9 140449886 140449886 single base substitution G A downstream_gene_variant STAD-US 9 140449886 140449886 single base substitution G A exon_variant STAD-US 9 140449886 140449886 single base substitution G A synonymous_variant G388G 1164C>T STAD-US 9 140468751 140468751 deletion of <=200bp G - downstream_gene_variant STAD-US 9 140468751 140468751 deletion of <=200bp G - exon_variant STAD-US 9 140468751 140468751 deletion of <=200bp G - frameshift_variant P183 STAD-US 9 140468755 140468755 single base substitution C A downstream_gene_variant STAD-US 9 140468755 140468755 single base substitution C A exon_variant STAD-US 9 140468755 140468755 single base substitution C A missense_variant R182M 545G>T STAD-US 9 140469211 140469211 deletion of <=200bp T - downstream_gene_variant STAD-US 9 140469211 140469211 deletion of <=200bp T - exon_variant STAD-US 9 140469211 140469211 deletion of <=200bp T - frameshift_variant T154 STAD-US 9 140476996 140476996 single base substitution C T upstream_gene_variant STAD-US 9 140477029 140477029 single base substitution C T upstream_gene_variant STAD-US 9 140477035 140477035 single base substitution C T upstream_gene_variant STAD-US 9 140477041 140477041 single base substitution C T upstream_gene_variant STAD-US 9 140477600 140477600 single base substitution A C upstream_gene_variant THCA-SA 9 140449582 140449582 single base substitution A C 3_prime_UTR_variant THCA-SA 9 140449582 140449582 single base substitution A C downstream_gene_variant THCA-SA 9 140449582 140449582 single base substitution A C exon_variant THCA-SA 9 140476834 140476834 single base substitution G C upstream_gene_variant THCA-US 9 140446894 140446894 single base substitution C T downstream_gene_variant UCEC-US 9 140446740 140446740 single base substitution G T downstream_gene_variant UCEC-US 9 140450084 140450084 single base substitution C T downstream_gene_variant UCEC-US 9 140450084 140450084 single base substitution C T exon_variant UCEC-US 9 140450084 140450084 single base substitution C T synonymous_variant A322A 966G>A UCEC-US 9 140459602 140459602 single base substitution G A exon_variant UCEC-US 9 140459602 140459602 single base substitution G A synonymous_variant G215G 645C>T UCEC-US 9 140459602 140459602 single base substitution G A upstream_gene_variant UCEC-US 9 140477059 140477059 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand Pat_59_B COSM5875962 c.679G>A p.V227I Substitution - Missense 9:137565116-137565116 - TCGA-D9-A6EC-06 COSM4401418 c.460A>C p.T154P Substitution - Missense 9:137574759-137574759 - TCGA-AA-3492-01 COSM5097719 c.467+8C>T p.? Unknown 9:137574744-137574744 - B59-0-Tumor COSM1756079 c.154G>T p.G52C Substitution - Missense 9:137577603-137577603 - T1240 COSM4741107 c.402C>T p.S134S Substitution - coding silent 9:137574817-137574817 - B90 COSM1756079 c.154G>T p.G52C Substitution - Missense 9:137577603-137577603 - TARGET-30-PASAZJ COSM1288958 c.162G>T p.M54I Substitution - Missense 9:137577595-137577595 - B104-0 COSM1756076 c.1342G>C p.E448Q Substitution - Missense 9:137555256-137555256 - LUAD-B01811 COSM355872 c.1046A>T p.Q349L Substitution - Missense 9:137555552-137555552 - 585208 COSM326879 c.850G>T p.G284W Substitution - Missense 9:137564533-137564533 - TCGA-66-2785-01 COSM753021 c.1209G>A p.M403I Substitution - Missense 9:137555389-137555389 - TCGA-HC-7232-01 COSM4393605 c.1048C>T p.R350W Substitution - Missense 9:137555550-137555550 - HCT15 COSM4626408 c.1096G>T p.D366Y Substitution - Missense 9:137555502-137555502 - B104-0-Tumor COSM1756077 c.1132C>T p.H378Y Substitution - Missense 9:137555466-137555466 - EOPC-01_tumor COSM3716678 c.836C>T p.T279M Substitution - Missense 9:137564547-137564547 - TCGA-FW-A3R5-06 COSM3926517 c.507C>T p.S169S Substitution - coding silent 9:137574341-137574341 - 2178 COSM4987553 c.824C>T p.P275L Substitution - Missense 9:137564559-137564559 - SC_9047 COSM5572139 c.669G>T p.W223C Substitution - Missense 9:137565126-137565126 - T578 COSM4741106 c.459A>C p.K153N Substitution - Missense 9:137574760-137574760 - CHC1743T COSM4805599 c.53C>A p.S18* Substitution - Nonsense 9:137578725-137578725 - 2218458 COSM4421210 c.835A>C p.T279P Substitution - Missense 9:137564548-137564548 - CHC1743T COSM4805599 c.53C>A p.S18* Substitution - Nonsense 9:137578725-137578725 - ESCC_BICR_024T COSM3656068 c.982C>T p.H328Y Substitution - Missense 9:137555616-137555616 - PD4123a COSM165593 c.502G>A p.D168N Substitution - Missense 9:137574346-137574346 - ML_41_T_01 COSM5033761 c.146A>C p.Q49P Substitution - Missense 9:137578632-137578632 - B104-0-Tumor COSM1756076 c.1342G>C p.E448Q Substitution - Missense 9:137555256-137555256 - S00945 COSM316556 c.1069C>T p.P357S Substitution - Missense 9:137555529-137555529 - ESCC_146 COSM5644744 c.1195C>T p.L399F Substitution - Missense 9:137555403-137555403 - DLD1 COSM4626408 c.1096G>T p.D366Y Substitution - Missense 9:137555502-137555502 - 91698 COSM330553 c.913A>C p.S305R Substitution - Missense 9:137564470-137564470 - PA285 COSM1163533 c.647A>G p.D216G Substitution - Missense 9:137565148-137565148 - CHC1209T COSM4804710 c.864C>T p.I288I Substitution - coding silent 9:137564519-137564519 - B90 COSM1756078 c.282G>A p.M94I Substitution - Missense 9:137577475-137577475 - Pat_63_B COSM5875961 c.1127C>T p.P376L Substitution - Missense 9:137555471-137555471 - TCGA-D1-A17A-01 COSM1107155 c.846G>T p.Q282H Substitution - Missense 9:137564537-137564537 - TCGA-A6-5661-01 COSM5089233 c.589G>A p.E197K Substitution - Missense 9:137574259-137574259 - TCGA-QG-A5Z2-01 COSM5187989 c.385G>A p.V129M Substitution - Missense 9:137574834-137574834 - SWE-25 COSM1179209 c.932A>G p.N311S Substitution - Missense 9:137564451-137564451 - T2269 COSM4741103 c.1188G>T p.M396I Substitution - Missense 9:137555410-137555410 - B90-Tumor COSM1756078 c.282G>A p.M94I Substitution - Missense 9:137577475-137577475 - TCGA-BP-4170-01 COSM3367659 c.1151A>C p.N384T Substitution - Missense 9:137555447-137555447 - TARGET-30-PASAZJ-01A-01W COSM1288958 c.162G>T p.M54I Substitution - Missense 9:137577595-137577595 - TCGA-EE-A29D-06 COSM3656066 c.1020G>A p.W340* Substitution - Nonsense 9:137555578-137555578 - TCGA-AA-3680-01 COSM293039 c.837G>A p.T279T Substitution - coding silent 9:137564546-137564546 - PD18024a COSM5777285 c.198C>T p.L66L Substitution - coding silent 9:137577559-137577559 - 12924 COSM5616109 c.941A>T p.K314M Substitution - Missense 9:137564442-137564442 - TCGA-G4-6320-01 COSM3699606 c.751C>T p.R251W Substitution - Missense 9:137564918-137564918 - TCGA-CG-4465-01 COSM3906144 c.1164C>T p.G388G Substitution - coding silent 9:137555434-137555434 - TCGA-DA-A3F8-06 COSM1701987 c.464G>A p.G155E Substitution - Missense 9:137574755-137574755 - SNU-C2B COSM1107155 c.846G>T p.Q282H Substitution - Missense 9:137564537-137564537 - TCGA-J4-A67L-01 COSM4391896 c.546G>C p.R182S Substitution - Missense 9:137574302-137574302 - S02294 COSM5688944 c.402delC p.S135fs*13 Deletion - Frameshift 9:137574817-137574817 - TCGA-BR-7901-01 COSM3906145 c.545G>T p.R182M Substitution - Missense 9:137574303-137574303 - B59-0 COSM1756079 c.154G>T p.G52C Substitution - Missense 9:137577603-137577603 - OSCC-GB_00800111 COSM1701986 c.1058C>T p.S353L Substitution - Missense 9:137555540-137555540 - ESCC_BICR_040T COSM5430235 c.243C>G p.V81V Substitution - coding silent 9:137577514-137577514 - TCGA-B5-A0JY-01 COSM1107154 c.966G>A p.A322A Substitution - coding silent 9:137555632-137555632 - T3535 COSM4741105 c.573G>A p.W191* Substitution - Nonsense 9:137574275-137574275 - B90-Tumor COSM1756079 c.154G>T p.G52C Substitution - Missense 9:137577603-137577603 - TCGA-EE-A180-06 COSM3656067 c.998C>T p.S333L Substitution - Missense 9:137555600-137555600 - S00945 COSM316556 c.1069C>T p.P357S Substitution - Missense 9:137555529-137555529 - 8030032 COSM3395702 c.294C>T p.H98H Substitution - coding silent 9:137576161-137576161 - TCGA-D8-A1XJ-01 COSM1489847 c.1179G>A p.Q393Q Substitution - coding silent 9:137555419-137555419 - PT33 COSM5908965 c.467+8C>G p.? Unknown 9:137574744-137574744 - RK100_C01 COSM1636104 c.1167T>C p.H389H Substitution - coding silent 9:137555431-137555431 - T3724 COSM4741104 c.661A>G p.R221G Substitution - Missense 9:137565134-137565134 - AOCS-079-1-1 COSM4152206 c.1156G>C p.G386R Substitution - Missense 9:137555442-137555442 - TCGA-EE-A2GC-06 COSM3656068 c.982C>T p.H328Y Substitution - Missense 9:137555616-137555616 - 2218458 COSM4421209 c.844C>A p.Q282K Substitution - Missense 9:137564539-137564539 - I2L-P19Tb-Tumor-Organoid COSM5367765 c.644_645insG p.D216fs*46 Insertion - Frameshift 9:137565150-137565151 - QC2-39-T2 COSM5655625 c.696C>G p.L232L Substitution - coding silent 9:137565099-137565099 - CHC1209T COSM4804710 c.864C>T p.I288I Substitution - coding silent 9:137564519-137564519 - TCGA-CM-4744-01 COSM1461418 c.825G>A p.P275P Substitution - coding silent 9:137564558-137564558 - SC_9063 COSM5574112 c.287+5_287+6insT p.? Unknown 9:137577464-137577465 - TCGA-B5-A11E-01 COSM1107156 c.645C>T p.G215G Substitution - coding silent 9:137565150-137565150 - B104-0 COSM1756077 c.1132C>T p.H378Y Substitution - Missense 9:137555466-137555466 - TCGA-AY-6196-01 COSM3699607 c.76G>T p.G26C Substitution - Missense 9:137578702-137578702 - YUKLAB COSM1701986 c.1058C>T p.S353L Substitution - Missense 9:137555540-137555540 - TCGA-AS-3777-01 COSM1497009 c.435G>A p.L145L Substitution - coding silent 9:137574784-137574784 - TCGA-D3-A1Q4-06 COSM3656069 c.927C>T p.I309I Substitution - coding silent 9:137564456-137564456 - YUGAFFE COSM1701987 c.464G>A p.G155E Substitution - Missense 9:137574755-137574755 - TCGA-43-6143-01 COSM753020 c.565G>A p.A189T Substitution - Missense 9:137574283-137574283 - CCK81 COSM1107156 c.645C>T p.G215G Substitution - coding silent 9:137565150-137565150 - RMS111_ COSM4987553 c.824C>T p.P275L Substitution - Missense 9:137564559-137564559 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.292570 9q34.3 613210

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Synonymous p.D217D c.651T>C 9 140459596 MM A G Synonymous p.H389H c.1167T>C 9 140449883 HC C A Missense p.G284W c.850G>T 9 140458985 SCLC C A Missense p.M54I c.162G>T 9 140472047 NB C G Missense p.R182S c.546G>C 9 140468754 PRAD C T Missense p.A189T c.565G>A 9 140468735 LUSC C T Missense p.D168N c.502G>A 9 140468798 BRCA C T Missense p.G155E c.464G>A 9 140469207 CM C T Synonymous p.Q393Q c.1179G>A 9 140449871 BRCA C T Synonymous p.T279T c.837G>A 9 140458998 COREAD G A IntronicSNV . c.641-41C>T 9 140459647 CM G A Missense p.H328Y c.982C>T 9 140450068 CM G A Missense p.P357S c.1069C>T 9 140449981 SCLC G A Missense p.R350W c.1048C>T 9 140450002 PRAD G A Missense p.S333L c.998C>T 9 140450052 CM G A Synonymous p.D159D c.477C>T 9 140468823 CM G A Synonymous p.G388G c.1164C>T 9 140449886 STAD G A Synonymous p.I309I c.927C>T 9 140458908 CM G A Synonymous p.T15T c.45C>T 9 140473185 HNSC G - IntronicDeletion . c.711-62delC 9 140459472 RCCC T A Missense p.K314M c.941A>T 9 140458894 NSCLC T G Missense p.N384T c.1151A>C 9 140449899 RCCC T G Missense p.Y260S c.779A>C 9 140459056 BRCA T - IntronicDeletion . c.467+148delA 9 140469056 STAD