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 7 72727177 72727177 + Frame_Shift_Del DEL G G - TCGA-CF-A47S-01A-11D-A23U-08 TCGA-CF-A47S-10A-01D-A23U-08 g.chr7:72727177delG c.1204delC c.(1204-1206)cggfs p.R402fs BLCA 7 72738485 72738485 + Missense_Mutation SNP C C G TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr7:72738485C>G c.301G>C c.(301-303)Gag>Cag p.E101Q BLCA 7 72738498 72738498 + Silent SNP G G C TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr7:72738498G>C c.288C>G c.(286-288)ctC>ctG p.L96L BLCA 7 72738632 72738632 + Missense_Mutation SNP G G A TCGA-FD-A3SN-01A-12D-A22Z-08 TCGA-FD-A3SN-10A-01D-A22Z-08 g.chr7:72738632G>A c.154C>T c.(154-156)Cgc>Tgc p.R52C BRCA 7 72727112 72727112 + Silent SNP G G T TCGA-A2-A25E-01A-11D-A167-09 TCGA-A2-A25E-10A-01D-A167-09 g.chr7:72727112G>T c.1269C>A c.(1267-1269)ggC>ggA p.G423G BRCA 7 72730631 72730632 + Frame_Shift_Ins INS - - T TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr7:72730631_72730632insT c.806_807insA c.(805-807)aagfs p.K269fs BRCA 7 72732851 72732851 + Silent SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr7:72732851G>A c.696C>T c.(694-696)ttC>ttT p.F232F BRCA 7 72738405 72738405 + Silent SNP G G A TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr7:72738405G>A c.381C>T c.(379-381)acC>acT p.T127T BRCA 7 72738436 72738436 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr7:72738436T>G c.350A>C c.(349-351)cAc>cCc p.H117P CESC 7 72732856 72732856 + Nonsense_Mutation SNP G G A TCGA-FU-A5XV-01A-11D-A28B-09 TCGA-FU-A5XV-10A-01D-A28E-09 g.chr7:72732856G>A c.691C>T c.(691-693)Cag>Tag p.Q231* COAD 7 72726959 72726959 + Silent SNP G G A TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr7:72726959G>A c.1422C>T c.(1420-1422)agC>agT p.S474S COAD 7 72727138 72727138 + Missense_Mutation SNP C C T TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr7:72727138C>T c.1243G>A c.(1243-1245)Ggg>Agg p.G415R COAD 7 72727343 72727343 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr7:72727343G>A c.1038C>T c.(1036-1038)tgC>tgT p.C346C COAD 7 72727384 72727384 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr7:72727384C>T c.997G>A c.(997-999)Gac>Aac p.D333N COAD 7 72732871 72732871 + Missense_Mutation SNP C C T TCGA-AA-3681-01A-01W-0900-09 TCGA-AA-3681-10A-01W-0900-09 g.chr7:72732871C>T c.676G>A c.(676-678)Gag>Aag p.E226K COAD 7 72732998 72732998 + Silent SNP G G A TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr7:72732998G>A c.549C>T c.(547-549)caC>caT p.H183H COADREAD 7 72726959 72726959 + Silent SNP G G A TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr7:72726959G>A c.1422C>T c.(1420-1422)agC>agT p.S474S COADREAD 7 72727138 72727138 + Missense_Mutation SNP C C T TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr7:72727138C>T c.1243G>A c.(1243-1245)Ggg>Agg p.G415R COADREAD 7 72727343 72727343 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr7:72727343G>A c.1038C>T c.(1036-1038)tgC>tgT p.C346C COADREAD 7 72727384 72727384 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr7:72727384C>T c.997G>A c.(997-999)Gac>Aac p.D333N COADREAD 7 72732851 72732851 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr7:72732851G>A c.696C>T c.(694-696)ttC>ttT p.F232F COADREAD 7 72732871 72732871 + Missense_Mutation SNP C C T TCGA-AA-3681-01A-01W-0900-09 TCGA-AA-3681-10A-01W-0900-09 g.chr7:72732871C>T c.676G>A c.(676-678)Gag>Aag p.E226K COADREAD 7 72732998 72732998 + Silent SNP G G A TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr7:72732998G>A c.549C>T c.(547-549)caC>caT p.H183H DLBC 7 72732848 72732848 + Silent SNP G G T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr7:72732848G>T c.699C>A c.(697-699)ggC>ggA p.G233G DLBC 7 72738638 72738638 + Missense_Mutation SNP C C T TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr7:72738638C>T c.148G>A c.(148-150)Gag>Aag p.E50K ESCA 7 72727162 72727162 + Missense_Mutation SNP C C T TCGA-R6-A6DN-01B-11D-A31U-09 TCGA-R6-A6DN-10A-01D-A31U-09 g.chr7:72727162C>T c.1219G>A c.(1219-1221)Gtg>Atg p.V407M ESCA 7 72734220 72734220 + Missense_Mutation SNP A A G TCGA-VR-A8EQ-01A-11D-A36J-09 TCGA-VR-A8EQ-10A-01D-A36M-09 g.chr7:72734220A>G c.421T>C c.(421-423)Tct>Cct p.S141P GBM 7 72734159 72734159 + Missense_Mutation SNP C C T TCGA-26-5136-01B-01D-1486-08 TCGA-26-5136-10A-01D-1486-08 g.chr7:72734159C>T c.482G>A c.(481-483)cGg>cAg p.R161Q GBMLGG 7 72732892 72732892 + Missense_Mutation SNP G G A TCGA-S9-A7QW-01A-11D-A34A-08 TCGA-S9-A7QW-10A-01D-A34A-08 g.chr7:72732892G>A c.655C>T c.(655-657)Cgg>Tgg p.R219W GBMLGG 7 72732972 72732972 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:72732972C>T c.575G>A c.(574-576)cGc>cAc p.R192H GBMLGG 7 72734159 72734159 + Missense_Mutation SNP C C T TCGA-26-5136-01B-01D-1486-08 TCGA-26-5136-10A-01D-1486-08 g.chr7:72734159C>T c.482G>A c.(481-483)cGg>cAg p.R161Q HNSC 7 72730600 72730600 + Missense_Mutation SNP T T C TCGA-CQ-6227-01A-11D-1912-08 TCGA-CQ-6227-10A-01D-1912-08 g.chr7:72730600T>C c.838A>G c.(838-840)Acc>Gcc p.T280A HNSC 7 72738498 72738498 + Silent SNP G G C TCGA-F7-8489-01A-31D-2394-08 TCGA-F7-8489-10A-01D-2394-08 g.chr7:72738498G>C c.288C>G c.(286-288)ctC>ctG p.L96L KICH 7 72734197 72734197 + Silent SNP T T C TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chr7:72734197T>C c.444A>G c.(442-444)aaA>aaG p.K148K KIPAN 7 72732707 72732707 + Splice_Site SNP T T A TCGA-CZ-5461-01A-01D-1501-10 TCGA-CZ-5461-11A-01D-1501-10 g.chr7:72732707T>A c.728A>T c.(727-729)aAg>aTg p.K243M KIPAN 7 72734197 72734197 + Silent SNP T T C TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chr7:72734197T>C c.444A>G c.(442-444)aaA>aaG p.K148K KIRC 7 72732707 72732707 + Splice_Site SNP T T A TCGA-CZ-5461-01A-01D-1501-10 TCGA-CZ-5461-11A-01D-1501-10 g.chr7:72732707T>A c.728A>T c.(727-729)aAg>aTg p.K243M LGG 7 72732892 72732892 + Missense_Mutation SNP G G A TCGA-S9-A7QW-01A-11D-A34A-08 TCGA-S9-A7QW-10A-01D-A34A-08 g.chr7:72732892G>A c.655C>T c.(655-657)Cgg>Tgg p.R219W LGG 7 72732972 72732972 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:72732972C>T c.575G>A c.(574-576)cGc>cAc p.R192H LUAD 7 72727232 72727232 + Silent SNP G G A TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr7:72727232G>A c.1149C>T c.(1147-1149)ggC>ggT p.G383G LUAD 7 72727283 72727283 + Silent SNP G G A TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr7:72727283G>A c.1098C>T c.(1096-1098)atC>atT p.I366I LUAD 7 72730668 72730668 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr7:72730668C>A c.770G>T c.(769-771)cGg>cTg p.R257L LUAD 7 72732960 72732960 + Missense_Mutation SNP C C A TCGA-05-5420-01A-01D-1625-08 TCGA-05-5420-11A-01D-1625-08 g.chr7:72732960C>A c.587G>T c.(586-588)gGg>gTg p.G196V LUAD 7 72734169 72734169 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr7:72734169C>A c.472G>T c.(472-474)Gtg>Ttg p.V158L LUAD 7 72734212 72734212 + Silent SNP C C T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr7:72734212C>T c.429G>A c.(427-429)ctG>ctA p.L143L LUAD 7 72738406 72738406 + Missense_Mutation SNP G G T TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr7:72738406G>T c.380C>A c.(379-381)aCc>aAc p.T127N LUAD 7 72738485 72738485 + Nonsense_Mutation SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr7:72738485C>A c.301G>T c.(301-303)Gag>Tag p.E101* LUAD 7 72738498 72738498 + Silent SNP G G C TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr7:72738498G>C c.288C>G c.(286-288)ctC>ctG p.L96L LUAD 7 72738530 72738530 + Missense_Mutation SNP G G C TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr7:72738530G>C c.256C>G c.(256-258)Ccc>Gcc p.P86A LUSC 7 72727109 72727109 + Missense_Mutation SNP T T G TCGA-66-2781-01A-01D-1522-08 TCGA-66-2781-11A-01D-1522-08 g.chr7:72727109T>G c.1272A>C c.(1270-1272)gaA>gaC p.E424D LUSC 7 72732870 72732870 + Missense_Mutation SNP T T A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr7:72732870T>A c.677A>T c.(676-678)gAg>gTg p.E226V LUSC 7 72734219 72734219 + Missense_Mutation SNP G G T TCGA-21-1076-01A-02D-1521-08 TCGA-21-1076-11A-01D-1521-08 g.chr7:72734219G>T c.422C>A c.(421-423)tCt>tAt p.S141Y OV 7 72727266 72727266 + Missense_Mutation SNP C C T TCGA-13-2057-01A-02D-1526-09 TCGA-13-2057-10A-01D-1526-09 g.chr7:72727266C>T c.1115G>A c.(1114-1116)cGt>cAt p.R372H PAAD 7 72734178 72734178 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr7:72734178C>T c.463G>A c.(463-465)Gcc>Acc p.A155T PAAD 7 72738607 72738607 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr7:72738607A>G c.179T>C c.(178-180)gTg>gCg p.V60A READ 7 72732851 72732851 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr7:72732851G>A c.696C>T c.(694-696)ttC>ttT p.F232F SKCM 7 72727133 72727133 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr7:72727133G>A c.1248C>T c.(1246-1248)ctC>ctT p.L416L SKCM 7 72730583 72730583 + Silent SNP G G A TCGA-EE-A3JH-06A-11D-A21A-08 TCGA-EE-A3JH-10A-01D-A21A-08 g.chr7:72730583G>A c.855C>T c.(853-855)ctC>ctT p.L285L SKCM 7 72732989 72732989 + Silent SNP C C T TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr7:72732989C>T c.558G>A c.(556-558)gtG>gtA p.V186V SKCM 7 72738546 72738546 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr7:72738546G>A c.240C>T c.(238-240)ctC>ctT p.L80L SKCM 7 72738612 72738612 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr7:72738612C>T c.174G>A c.(172-174)caG>caA p.Q58Q SKCM 7 72738661 72738661 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr7:72738661G>A c.125C>T c.(124-126)tCc>tTc p.S42F

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 7 72738450 72738450 single base substitution A C exon_variant BLCA-CN 7 72738450 72738450 single base substitution A C synonymous_variant G112G 336T>G BLCA-CN 7 72738607 72738607 single base substitution A C exon_variant BLCA-CN 7 72738607 72738607 single base substitution A C missense_variant V60G 179T>G BLCA-CN 7 72742399 72742399 single base substitution G A upstream_gene_variant BLCA-US 7 72721626 72721626 single base substitution C T downstream_gene_variant BLCA-US 7 72738632 72738632 single base substitution G A exon_variant BLCA-US 7 72738632 72738632 single base substitution G A missense_variant R52C 154C>T BOCA-FR 7 72731987 72731987 single base substitution T C downstream_gene_variant BOCA-FR 7 72731987 72731987 single base substitution T C intron_variant BOCA-FR 7 72731987 72731987 single base substitution T C upstream_gene_variant BRCA-EU 7 72722069 72722069 single base substitution C T downstream_gene_variant BRCA-EU 7 72722743 72722743 single base substitution C T downstream_gene_variant BRCA-EU 7 72725023 72725023 single base substitution G A downstream_gene_variant BRCA-EU 7 72726266 72726266 single base substitution C A downstream_gene_variant BRCA-EU 7 72726584 72726584 single base substitution G A 3_prime_UTR_variant BRCA-EU 7 72726584 72726584 single base substitution G A downstream_gene_variant BRCA-EU 7 72726826 72726826 single base substitution G A 3_prime_UTR_variant BRCA-EU 7 72726826 72726826 single base substitution G A downstream_gene_variant BRCA-EU 7 72727542 72727542 single base substitution G A intron_variant BRCA-EU 7 72728615 72728615 single base substitution G A intron_variant BRCA-EU 7 72730425 72730425 single base substitution C T intron_variant BRCA-EU 7 72731365 72731365 insertion of <=200bp - TG downstream_gene_variant BRCA-EU 7 72731365 72731365 insertion of <=200bp - TG intron_variant BRCA-EU 7 72731365 72731365 insertion of <=200bp - TG upstream_gene_variant BRCA-EU 7 72732342 72732342 single base substitution G A downstream_gene_variant BRCA-EU 7 72732342 72732342 single base substitution G A intron_variant BRCA-EU 7 72732342 72732342 single base substitution G A upstream_gene_variant BRCA-EU 7 72732754 72732754 single base substitution T C downstream_gene_variant BRCA-EU 7 72732754 72732754 single base substitution T C intron_variant BRCA-EU 7 72732754 72732754 single base substitution T C upstream_gene_variant BRCA-EU 7 72734338 72734338 single base substitution C A downstream_gene_variant BRCA-EU 7 72734338 72734338 single base substitution C A intron_variant BRCA-EU 7 72734338 72734338 single base substitution C A upstream_gene_variant BRCA-EU 7 72734696 72734696 single base substitution C G downstream_gene_variant BRCA-EU 7 72734696 72734696 single base substitution C G intron_variant BRCA-EU 7 72734696 72734696 single base substitution C G upstream_gene_variant BRCA-EU 7 72734923 72734923 single base substitution T C downstream_gene_variant BRCA-EU 7 72734923 72734923 single base substitution T C intron_variant BRCA-EU 7 72734923 72734923 single base substitution T C upstream_gene_variant BRCA-EU 7 72734956 72734956 single base substitution G C downstream_gene_variant BRCA-EU 7 72734956 72734956 single base substitution G C intron_variant BRCA-EU 7 72734956 72734956 single base substitution G C upstream_gene_variant BRCA-EU 7 72735168 72735168 deletion of <=200bp T - downstream_gene_variant BRCA-EU 7 72735168 72735168 deletion of <=200bp T - intron_variant BRCA-EU 7 72735168 72735168 deletion of <=200bp T - upstream_gene_variant BRCA-EU 7 72735593 72735593 single base substitution G A downstream_gene_variant BRCA-EU 7 72735593 72735593 single base substitution G A intron_variant BRCA-EU 7 72735593 72735593 single base substitution G A upstream_gene_variant BRCA-EU 7 72736272 72736272 single base substitution C T intron_variant BRCA-EU 7 72736311 72736311 single base substitution G A intron_variant BRCA-EU 7 72736526 72736526 single base substitution C A intron_variant BRCA-EU 7 72736916 72736916 single base substitution C T intron_variant BRCA-EU 7 72738561 72738561 single base substitution G A exon_variant BRCA-EU 7 72738561 72738561 single base substitution G A synonymous_variant I75I 225C>T BRCA-EU 7 72738806 72738806 single base substitution G A splice_region_variant BRCA-EU 7 72739172 72739172 single base substitution G A intron_variant BRCA-EU 7 72740013 72740013 single base substitution G A intron_variant BRCA-EU 7 72740013 72740013 single base substitution G A upstream_gene_variant BRCA-EU 7 72740295 72740295 single base substitution A G intron_variant BRCA-EU 7 72740295 72740295 single base substitution A G upstream_gene_variant BRCA-EU 7 72741076 72741076 single base substitution G C intron_variant BRCA-EU 7 72741076 72741076 single base substitution G C upstream_gene_variant BRCA-EU 7 72742201 72742201 single base substitution G A upstream_gene_variant BRCA-EU 7 72742817 72742817 single base substitution G C upstream_gene_variant BRCA-EU 7 72744018 72744018 single base substitution G A upstream_gene_variant BRCA-EU 7 72746016 72746016 single base substitution G A upstream_gene_variant BRCA-EU 7 72746065 72746065 single base substitution C T upstream_gene_variant BRCA-EU 7 72746573 72746573 single base substitution G A upstream_gene_variant BRCA-FR 7 72726826 72726826 single base substitution G A 3_prime_UTR_variant BRCA-FR 7 72726826 72726826 single base substitution G A downstream_gene_variant BRCA-FR 7 72728615 72728615 single base substitution G A intron_variant BRCA-FR 7 72730145 72730145 single base substitution G T intron_variant BRCA-FR 7 72732754 72732754 single base substitution T C downstream_gene_variant BRCA-FR 7 72732754 72732754 single base substitution T C intron_variant BRCA-FR 7 72732754 72732754 single base substitution T C upstream_gene_variant BRCA-FR 7 72735593 72735593 single base substitution G A downstream_gene_variant BRCA-FR 7 72735593 72735593 single base substitution G A intron_variant BRCA-FR 7 72735593 72735593 single base substitution G A upstream_gene_variant BRCA-FR 7 72741076 72741076 single base substitution G C intron_variant BRCA-FR 7 72741076 72741076 single base substitution G C upstream_gene_variant BRCA-FR 7 72746065 72746065 single base substitution C T upstream_gene_variant BRCA-US 7 72727112 72727112 single base substitution G T downstream_gene_variant BRCA-US 7 72727112 72727112 single base substitution G T synonymous_variant G423G 1269C>A BRCA-US 7 72730631 72730631 insertion of <=200bp - T exon_variant BRCA-US 7 72730631 72730631 insertion of <=200bp - T frameshift_variant K269K? BRCA-US 7 72732851 72732851 single base substitution G A downstream_gene_variant BRCA-US 7 72732851 72732851 single base substitution G A synonymous_variant F232F 696C>T BRCA-US 7 72732851 72732851 single base substitution G A upstream_gene_variant BRCA-US 7 72738405 72738405 single base substitution G A exon_variant BRCA-US 7 72738405 72738405 single base substitution G A synonymous_variant T127T 381C>T BRCA-US 7 72738436 72738436 single base substitution T G exon_variant BRCA-US 7 72738436 72738436 single base substitution T G missense_variant H117P 350A>C BTCA-JP 7 72721557 72721557 single base substitution C A downstream_gene_variant CESC-US 7 72721671 72721671 single base substitution C T downstream_gene_variant CESC-US 7 72732856 72732856 single base substitution G A downstream_gene_variant CESC-US 7 72732856 72732856 single base substitution G A stop_gained Q231* 691C>T CESC-US 7 72732856 72732856 single base substitution G A upstream_gene_variant COAD-US 7 72726959 72726959 single base substitution G A downstream_gene_variant COAD-US 7 72726959 72726959 single base substitution G A synonymous_variant S474S 1422C>T COAD-US 7 72726987 72726987 single base substitution G A downstream_gene_variant COAD-US 7 72726987 72726987 single base substitution G A missense_variant S465L 1394C>T COAD-US 7 72727138 72727138 single base substitution C T downstream_gene_variant COAD-US 7 72727138 72727138 single base substitution C T missense_variant G415R 1243G>A COAD-US 7 72727343 72727343 single base substitution G A exon_variant COAD-US 7 72727343 72727343 single base substitution G A synonymous_variant C346C 1038C>T COAD-US 7 72727384 72727384 single base substitution C T exon_variant COAD-US 7 72727384 72727384 single base substitution C T missense_variant D333N 997G>A COAD-US 7 72727439 72727439 single base substitution C T exon_variant COAD-US 7 72727439 72727439 single base substitution C T synonymous_variant T314T 942G>A COAD-US 7 72732998 72732998 single base substitution G A downstream_gene_variant COAD-US 7 72732998 72732998 single base substitution G A synonymous_variant H183H 549C>T COAD-US 7 72732998 72732998 single base substitution G A upstream_gene_variant COAD-US 7 72738561 72738561 single base substitution G T exon_variant COAD-US 7 72738561 72738561 single base substitution G T synonymous_variant I75I 225C>A COAD-US 7 72742434 72742434 deletion of <=200bp G - upstream_gene_variant COAD-US 7 72743414 72743414 single base substitution A G upstream_gene_variant COAD-US 7 72745721 72745721 single base substitution T G upstream_gene_variant COAD-US 7 72745752 72745752 single base substitution C A upstream_gene_variant COCA-CN 7 72722981 72722981 single base substitution G A downstream_gene_variant COCA-CN 7 72727196 72727196 single base substitution G A downstream_gene_variant COCA-CN 7 72727196 72727196 single base substitution G A synonymous_variant Y395Y 1185C>T COCA-CN 7 72727343 72727343 single base substitution G A exon_variant COCA-CN 7 72727343 72727343 single base substitution G A synonymous_variant C346C 1038C>T COCA-CN 7 72727369 72727369 single base substitution C T exon_variant COCA-CN 7 72727369 72727369 single base substitution C T missense_variant V338I 1012G>A COCA-CN 7 72727580 72727580 single base substitution G T intron_variant COCA-CN 7 72732595 72732595 single base substitution G A downstream_gene_variant COCA-CN 7 72732595 72732595 single base substitution G A intron_variant COCA-CN 7 72732595 72732595 single base substitution G A upstream_gene_variant COCA-CN 7 72733119 72733119 single base substitution G A downstream_gene_variant COCA-CN 7 72733119 72733119 single base substitution G A intron_variant COCA-CN 7 72733119 72733119 single base substitution G A upstream_gene_variant COCA-CN 7 72738617 72738617 single base substitution G A exon_variant COCA-CN 7 72738617 72738617 single base substitution G A missense_variant R57W 169C>T COCA-CN 7 72738738 72738738 single base substitution A G exon_variant COCA-CN 7 72738738 72738738 single base substitution A G synonymous_variant C16C 48T>C ESAD-UK 7 72723105 72723105 single base substitution T A downstream_gene_variant ESAD-UK 7 72724616 72724616 single base substitution G A downstream_gene_variant ESAD-UK 7 72726255 72726255 single base substitution G A downstream_gene_variant ESAD-UK 7 72726701 72726701 single base substitution G A 3_prime_UTR_variant ESAD-UK 7 72726701 72726701 single base substitution G A downstream_gene_variant ESAD-UK 7 72727144 72727144 single base substitution G A downstream_gene_variant ESAD-UK 7 72727144 72727144 single base substitution G A missense_variant R413C 1237C>T ESAD-UK 7 72727235 72727235 single base substitution G A downstream_gene_variant ESAD-UK 7 72727235 72727235 single base substitution G A synonymous_variant H382H 1146C>T ESAD-UK 7 72728709 72728709 single base substitution G C intron_variant ESAD-UK 7 72729545 72729545 single base substitution C T intron_variant ESAD-UK 7 72729634 72729634 single base substitution G A intron_variant ESAD-UK 7 72729903 72729903 single base substitution G A intron_variant ESAD-UK 7 72733295 72733295 single base substitution T C downstream_gene_variant ESAD-UK 7 72733295 72733295 single base substitution T C intron_variant ESAD-UK 7 72733295 72733295 single base substitution T C upstream_gene_variant ESAD-UK 7 72733704 72733704 single base substitution G A downstream_gene_variant ESAD-UK 7 72733704 72733704 single base substitution G A intron_variant ESAD-UK 7 72733704 72733704 single base substitution G A upstream_gene_variant ESAD-UK 7 72734145 72734145 single base substitution C T downstream_gene_variant ESAD-UK 7 72734145 72734145 single base substitution C T splice_donor_variant ESAD-UK 7 72734145 72734145 single base substitution C T upstream_gene_variant ESAD-UK 7 72735658 72735658 single base substitution C T downstream_gene_variant ESAD-UK 7 72735658 72735658 single base substitution C T intron_variant ESAD-UK 7 72735658 72735658 single base substitution C T upstream_gene_variant ESAD-UK 7 72735755 72735755 single base substitution G A downstream_gene_variant ESAD-UK 7 72735755 72735755 single base substitution G A intron_variant ESAD-UK 7 72735755 72735755 single base substitution G A upstream_gene_variant ESAD-UK 7 72736016 72736016 single base substitution T A intron_variant ESAD-UK 7 72737531 72737531 insertion of <=200bp - TA intron_variant ESAD-UK 7 72738049 72738049 single base substitution G C intron_variant ESAD-UK 7 72741945 72741945 single base substitution G A 5_prime_UTR_variant ESAD-UK 7 72741945 72741945 single base substitution G A exon_variant ESAD-UK 7 72741945 72741945 single base substitution G A upstream_gene_variant ESAD-UK 7 72741987 72741987 single base substitution C T 5_prime_UTR_variant ESAD-UK 7 72741987 72741987 single base substitution C T upstream_gene_variant ESAD-UK 7 72742365 72742365 single base substitution C T upstream_gene_variant ESAD-UK 7 72743431 72743431 single base substitution C T upstream_gene_variant ESCA-CN 7 72729266 72729266 single base substitution C A intron_variant GBM-US 7 72721634 72721634 single base substitution G A downstream_gene_variant GBM-US 7 72721702 72721702 single base substitution C T downstream_gene_variant GBM-US 7 72722785 72722785 single base substitution C T downstream_gene_variant GBM-US 7 72734159 72734159 single base substitution C T downstream_gene_variant GBM-US 7 72734159 72734159 single base substitution C T missense_variant R161Q 482G>A GBM-US 7 72734159 72734159 single base substitution C T upstream_gene_variant GBM-US 7 72744235 72744235 single base substitution C T upstream_gene_variant KIRC-US 7 72732707 72732707 single base substitution T A downstream_gene_variant KIRC-US 7 72732707 72732707 single base substitution T A missense_variant K243M 728A>T KIRC-US 7 72732707 72732707 single base substitution T A upstream_gene_variant KIRC-US 7 72745747 72745747 single base substitution C T upstream_gene_variant LAML-KR 7 72728451 72728451 single base substitution C T intron_variant LAML-KR 7 72742309 72742309 single base substitution C T upstream_gene_variant LICA-FR 7 72727026 72727026 single base substitution G A downstream_gene_variant LICA-FR 7 72727026 72727026 single base substitution G A missense_variant P452L 1355C>T LICA-FR 7 72738629 72738629 single base substitution A G exon_variant LICA-FR 7 72738629 72738629 single base substitution A G missense_variant C53R 157T>C LICA-FR 7 72739013 72739022 deletion of <=200bp TGTGTGTGTG - intron_variant LICA-FR 7 72739738 72739738 single base substitution G A intron_variant LICA-FR 7 72739738 72739738 single base substitution G A upstream_gene_variant LICA-FR 7 72745684 72745684 single base substitution C G upstream_gene_variant LICA-FR 7 72745810 72745810 single base substitution T A upstream_gene_variant LINC-JP 7 72727861 72727861 single base substitution G C intron_variant LINC-JP 7 72727883 72727883 single base substitution G T intron_variant LINC-JP 7 72730125 72730125 single base substitution C T intron_variant LINC-JP 7 72730553 72730553 single base substitution C T intron_variant LINC-JP 7 72731423 72731423 single base substitution C A downstream_gene_variant LINC-JP 7 72731423 72731423 single base substitution C A intron_variant LINC-JP 7 72731423 72731423 single base substitution C A upstream_gene_variant LIRI-JP 7 72722180 72722180 single base substitution G A downstream_gene_variant LIRI-JP 7 72722714 72722714 single base substitution A G downstream_gene_variant LIRI-JP 7 72725513 72725513 single base substitution C T downstream_gene_variant LIRI-JP 7 72726811 72726811 single base substitution T C 3_prime_UTR_variant LIRI-JP 7 72726811 72726811 single base substitution T C downstream_gene_variant LIRI-JP 7 72727772 72727772 single base substitution T C intron_variant LIRI-JP 7 72728368 72728368 single base substitution C A intron_variant LIRI-JP 7 72729196 72729196 single base substitution A G intron_variant LIRI-JP 7 72731203 72731203 single base substitution C T downstream_gene_variant LIRI-JP 7 72731203 72731203 single base substitution C T intron_variant LIRI-JP 7 72731203 72731203 single base substitution C T upstream_gene_variant LIRI-JP 7 72732342 72732342 single base substitution G A downstream_gene_variant LIRI-JP 7 72732342 72732342 single base substitution G A intron_variant LIRI-JP 7 72732342 72732342 single base substitution G A upstream_gene_variant LIRI-JP 7 72734621 72734621 single base substitution T A downstream_gene_variant LIRI-JP 7 72734621 72734621 single base substitution T A intron_variant LIRI-JP 7 72734621 72734621 single base substitution T A upstream_gene_variant LIRI-JP 7 72741108 72741108 single base substitution T A intron_variant LIRI-JP 7 72741108 72741108 single base substitution T A upstream_gene_variant LIRI-JP 7 72742971 72742971 single base substitution G A upstream_gene_variant LIRI-JP 7 72745116 72745116 single base substitution T G upstream_gene_variant LIRI-JP 7 72745260 72745260 deletion of <=200bp T - upstream_gene_variant LIRI-JP 7 72746522 72746522 single base substitution A G upstream_gene_variant LIRI-JP 7 72746942 72746942 single base substitution A G upstream_gene_variant LUSC-KR 7 72727185 72727185 single base substitution G A downstream_gene_variant LUSC-KR 7 72727185 72727185 single base substitution G A missense_variant A399V 1196C>T LUSC-KR 7 72727303 72727303 single base substitution C A downstream_gene_variant LUSC-KR 7 72727303 72727303 single base substitution C A missense_variant D360Y 1078G>T LUSC-KR 7 72733175 72733175 single base substitution G T downstream_gene_variant LUSC-KR 7 72733175 72733175 single base substitution G T intron_variant LUSC-KR 7 72733175 72733175 single base substitution G T upstream_gene_variant LUSC-KR 7 72733580 72733580 single base substitution C A downstream_gene_variant LUSC-KR 7 72733580 72733580 single base substitution C A intron_variant LUSC-KR 7 72733580 72733580 single base substitution C A upstream_gene_variant LUSC-KR 7 72733581 72733581 single base substitution C A downstream_gene_variant LUSC-KR 7 72733581 72733581 single base substitution C A intron_variant LUSC-KR 7 72733581 72733581 single base substitution C A upstream_gene_variant LUSC-KR 7 72734285 72734285 single base substitution C A downstream_gene_variant LUSC-KR 7 72734285 72734285 single base substitution C A intron_variant LUSC-KR 7 72734285 72734285 single base substitution C A upstream_gene_variant LUSC-KR 7 72737299 72737299 single base substitution C A intron_variant LUSC-KR 7 72738668 72738668 single base substitution G C exon_variant LUSC-KR 7 72738668 72738668 single base substitution G C missense_variant L40V 118C>G LUSC-KR 7 72739900 72739900 single base substitution G A intron_variant LUSC-KR 7 72739900 72739900 single base substitution G A upstream_gene_variant LUSC-KR 7 72740879 72740879 single base substitution G A intron_variant LUSC-KR 7 72740879 72740879 single base substitution G A upstream_gene_variant LUSC-KR 7 72741870 72741870 single base substitution C A intron_variant LUSC-KR 7 72741870 72741870 single base substitution C A upstream_gene_variant LUSC-KR 7 72743403 72743403 single base substitution C T upstream_gene_variant LUSC-KR 7 72744450 72744450 single base substitution C T upstream_gene_variant LUSC-US 7 72727109 72727109 single base substitution T G downstream_gene_variant LUSC-US 7 72727109 72727109 single base substitution T G missense_variant E424D 1272A>C LUSC-US 7 72732870 72732870 single base substitution T A downstream_gene_variant LUSC-US 7 72732870 72732870 single base substitution T A missense_variant E226V 677A>T LUSC-US 7 72732870 72732870 single base substitution T A upstream_gene_variant LUSC-US 7 72734219 72734219 single base substitution G T downstream_gene_variant LUSC-US 7 72734219 72734219 single base substitution G T missense_variant S141Y 422C>A LUSC-US 7 72734219 72734219 single base substitution G T upstream_gene_variant LUSC-US 7 72742586 72742586 single base substitution C T upstream_gene_variant LUSC-US 7 72744195 72744195 single base substitution G A upstream_gene_variant LUSC-US 7 72744255 72744255 single base substitution G C upstream_gene_variant LUSC-US 7 72744316 72744316 single base substitution G A upstream_gene_variant MALY-DE 7 72726626 72726626 single base substitution C T 3_prime_UTR_variant MALY-DE 7 72726626 72726626 single base substitution C T downstream_gene_variant MALY-DE 7 72727667 72727667 insertion of <=200bp - TGAA intron_variant MALY-DE 7 72738552 72738552 single base substitution C T exon_variant MALY-DE 7 72738552 72738552 single base substitution C T synonymous_variant L78L 234G>A MELA-AU 7 72721742 72721742 single base substitution C T downstream_gene_variant MELA-AU 7 72722650 72722650 single base substitution G A downstream_gene_variant MELA-AU 7 72722850 72722850 single base substitution C T downstream_gene_variant MELA-AU 7 72722869 72722869 single base substitution C T downstream_gene_variant MELA-AU 7 72722870 72722870 single base substitution C T downstream_gene_variant MELA-AU 7 72722882 72722882 single base substitution G A downstream_gene_variant MELA-AU 7 72722935 72722935 single base substitution G A downstream_gene_variant MELA-AU 7 72723423 72723423 single base substitution C T downstream_gene_variant MELA-AU 7 72724042 72724042 single base substitution G T downstream_gene_variant MELA-AU 7 72724072 72724072 single base substitution C T downstream_gene_variant MELA-AU 7 72724161 72724161 single base substitution C T downstream_gene_variant MELA-AU 7 72725060 72725060 single base substitution C A downstream_gene_variant MELA-AU 7 72726014 72726014 single base substitution A G downstream_gene_variant MELA-AU 7 72726716 72726716 single base substitution C T 3_prime_UTR_variant MELA-AU 7 72726716 72726716 single base substitution C T downstream_gene_variant MELA-AU 7 72726769 72726769 single base substitution C T 3_prime_UTR_variant MELA-AU 7 72726769 72726769 single base substitution C T downstream_gene_variant MELA-AU 7 72726775 72726775 single base substitution C T 3_prime_UTR_variant MELA-AU 7 72726775 72726775 single base substitution C T downstream_gene_variant MELA-AU 7 72727139 72727139 single base substitution G A downstream_gene_variant MELA-AU 7 72727139 72727139 single base substitution G A synonymous_variant I414I 1242C>T MELA-AU 7 72727195 72727195 single base substitution C A downstream_gene_variant MELA-AU 7 72727195 72727195 single base substitution C A stop_gained E396* 1186G>T MELA-AU 7 72727292 72727292 single base substitution C T downstream_gene_variant MELA-AU 7 72727292 72727292 single base substitution C T synonymous_variant L363L 1089G>A MELA-AU 7 72727325 72727325 single base substitution C T downstream_gene_variant MELA-AU 7 72727325 72727325 single base substitution C T synonymous_variant E352E 1056G>A MELA-AU 7 72727497 72727497 single base substitution G A exon_variant MELA-AU 7 72727497 72727497 single base substitution G A missense_variant P295L 884C>T MELA-AU 7 72727657 72727657 single base substitution G A intron_variant MELA-AU 7 72727676 72727676 single base substitution G A intron_variant MELA-AU 7 72727890 72727890 single base substitution C T intron_variant MELA-AU 7 72728078 72728078 single base substitution C T intron_variant MELA-AU 7 72728147 72728147 single base substitution C T intron_variant MELA-AU 7 72728257 72728257 single base substitution C T intron_variant MELA-AU 7 72728274 72728274 single base substitution G A intron_variant MELA-AU 7 72728804 72728804 single base substitution C T intron_variant MELA-AU 7 72728870 72728870 single base substitution G A intron_variant MELA-AU 7 72729180 72729180 single base substitution G A intron_variant MELA-AU 7 72729450 72729450 single base substitution C T intron_variant MELA-AU 7 72729845 72729845 single base substitution C T intron_variant MELA-AU 7 72729854 72729854 single base substitution G A intron_variant MELA-AU 7 72729903 72729903 single base substitution G A intron_variant MELA-AU 7 72730419 72730419 single base substitution G A intron_variant MELA-AU 7 72730461 72730461 single base substitution C T intron_variant MELA-AU 7 72730467 72730467 single base substitution G A intron_variant MELA-AU 7 72730752 72730752 single base substitution C T exon_variant MELA-AU 7 72730752 72730752 single base substitution C T intron_variant MELA-AU 7 72730777 72730777 single base substitution C T exon_variant MELA-AU 7 72730777 72730777 single base substitution C T intron_variant MELA-AU 7 72730823 72730823 single base substitution C T exon_variant MELA-AU 7 72730823 72730823 single base substitution C T intron_variant MELA-AU 7 72730941 72730941 single base substitution C T downstream_gene_variant MELA-AU 7 72730941 72730941 single base substitution C T exon_variant MELA-AU 7 72730941 72730941 single base substitution C T intron_variant MELA-AU 7 72731432 72731432 single base substitution G A downstream_gene_variant MELA-AU 7 72731432 72731432 single base substitution G A intron_variant MELA-AU 7 72731432 72731432 single base substitution G A upstream_gene_variant MELA-AU 7 72731480 72731480 single base substitution C T downstream_gene_variant MELA-AU 7 72731480 72731480 single base substitution C T intron_variant MELA-AU 7 72731480 72731480 single base substitution C T upstream_gene_variant MELA-AU 7 72731857 72731857 single base substitution G T downstream_gene_variant MELA-AU 7 72731857 72731857 single base substitution G T intron_variant MELA-AU 7 72731857 72731857 single base substitution G T upstream_gene_variant MELA-AU 7 72732103 72732103 single base substitution C T downstream_gene_variant MELA-AU 7 72732103 72732103 single base substitution C T intron_variant MELA-AU 7 72732103 72732103 single base substitution C T upstream_gene_variant MELA-AU 7 72732253 72732253 single base substitution G A downstream_gene_variant MELA-AU 7 72732253 72732253 single base substitution G A intron_variant MELA-AU 7 72732253 72732253 single base substitution G A upstream_gene_variant MELA-AU 7 72732365 72732365 single base substitution G A downstream_gene_variant MELA-AU 7 72732365 72732365 single base substitution G A intron_variant MELA-AU 7 72732365 72732365 single base substitution G A upstream_gene_variant MELA-AU 7 72732375 72732375 single base substitution A G downstream_gene_variant MELA-AU 7 72732375 72732375 single base substitution A G intron_variant MELA-AU 7 72732375 72732375 single base substitution A G upstream_gene_variant MELA-AU 7 72732615 72732615 single base substitution G A downstream_gene_variant MELA-AU 7 72732615 72732615 single base substitution G A intron_variant MELA-AU 7 72732615 72732615 single base substitution G A upstream_gene_variant MELA-AU 7 72732674 72732674 single base substitution C T downstream_gene_variant MELA-AU 7 72732674 72732674 single base substitution C T intron_variant MELA-AU 7 72732674 72732674 single base substitution C T upstream_gene_variant MELA-AU 7 72732980 72732980 single base substitution C T downstream_gene_variant MELA-AU 7 72732980 72732980 single base substitution C T synonymous_variant E189E 567G>A MELA-AU 7 72732980 72732980 single base substitution C T upstream_gene_variant MELA-AU 7 72732989 72732989 single base substitution C T downstream_gene_variant MELA-AU 7 72732989 72732989 single base substitution C T synonymous_variant V186V 558G>A MELA-AU 7 72732989 72732989 single base substitution C T upstream_gene_variant MELA-AU 7 72733203 72733203 single base substitution T C downstream_gene_variant MELA-AU 7 72733203 72733203 single base substitution T C intron_variant MELA-AU 7 72733203 72733203 single base substitution T C upstream_gene_variant MELA-AU 7 72733231 72733231 single base substitution G A downstream_gene_variant MELA-AU 7 72733231 72733231 single base substitution G A intron_variant MELA-AU 7 72733231 72733231 single base substitution G A upstream_gene_variant MELA-AU 7 72733334 72733334 single base substitution C T downstream_gene_variant MELA-AU 7 72733334 72733334 single base substitution C T intron_variant MELA-AU 7 72733334 72733334 single base substitution C T upstream_gene_variant MELA-AU 7 72733509 72733509 single base substitution G A downstream_gene_variant MELA-AU 7 72733509 72733509 single base substitution G A intron_variant MELA-AU 7 72733509 72733509 single base substitution G A upstream_gene_variant MELA-AU 7 72733580 72733580 single base substitution C T downstream_gene_variant MELA-AU 7 72733580 72733580 single base substitution C T intron_variant MELA-AU 7 72733580 72733580 single base substitution C T upstream_gene_variant MELA-AU 7 72733590 72733590 single base substitution C T downstream_gene_variant MELA-AU 7 72733590 72733590 single base substitution C T intron_variant MELA-AU 7 72733590 72733590 single base substitution C T upstream_gene_variant MELA-AU 7 72733601 72733601 single base substitution G A downstream_gene_variant MELA-AU 7 72733601 72733601 single base substitution G A intron_variant MELA-AU 7 72733601 72733601 single base substitution G A upstream_gene_variant MELA-AU 7 72733779 72733779 single base substitution C T downstream_gene_variant MELA-AU 7 72733779 72733779 single base substitution C T intron_variant MELA-AU 7 72733779 72733779 single base substitution C T upstream_gene_variant MELA-AU 7 72733983 72733983 single base substitution C T downstream_gene_variant MELA-AU 7 72733983 72733983 single base substitution C T intron_variant MELA-AU 7 72733983 72733983 single base substitution C T upstream_gene_variant MELA-AU 7 72734276 72734276 single base substitution G A downstream_gene_variant MELA-AU 7 72734276 72734276 single base substitution G A intron_variant MELA-AU 7 72734276 72734276 single base substitution G A upstream_gene_variant MELA-AU 7 72734774 72734774 single base substitution C T downstream_gene_variant MELA-AU 7 72734774 72734774 single base substitution C T intron_variant MELA-AU 7 72734774 72734774 single base substitution C T upstream_gene_variant MELA-AU 7 72735502 72735502 single base substitution C T downstream_gene_variant MELA-AU 7 72735502 72735502 single base substitution C T intron_variant MELA-AU 7 72735502 72735502 single base substitution C T upstream_gene_variant MELA-AU 7 72735529 72735529 single base substitution G A downstream_gene_variant MELA-AU 7 72735529 72735529 single base substitution G A intron_variant MELA-AU 7 72735529 72735529 single base substitution G A upstream_gene_variant MELA-AU 7 72735617 72735618 multiple base substitution (>=2bp and <=200bp) GG AC downstream_gene_variant MELA-AU 7 72735617 72735618 multiple base substitution (>=2bp and <=200bp) GG AC intron_variant MELA-AU 7 72735617 72735618 multiple base substitution (>=2bp and <=200bp) GG AC upstream_gene_variant MELA-AU 7 72735645 72735645 single base substitution G A downstream_gene_variant MELA-AU 7 72735645 72735645 single base substitution G A intron_variant MELA-AU 7 72735645 72735645 single base substitution G A upstream_gene_variant MELA-AU 7 72735659 72735660 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 7 72735659 72735660 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 7 72735659 72735660 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 7 72735706 72735706 single base substitution C T downstream_gene_variant MELA-AU 7 72735706 72735706 single base substitution C T intron_variant MELA-AU 7 72735706 72735706 single base substitution C T upstream_gene_variant MELA-AU 7 72735893 72735893 single base substitution C T downstream_gene_variant MELA-AU 7 72735893 72735893 single base substitution C T intron_variant MELA-AU 7 72735893 72735893 single base substitution C T upstream_gene_variant MELA-AU 7 72736174 72736174 single base substitution C T intron_variant MELA-AU 7 72736256 72736256 single base substitution G A intron_variant MELA-AU 7 72736448 72736448 single base substitution C T intron_variant MELA-AU 7 72736835 72736835 single base substitution C T intron_variant MELA-AU 7 72736918 72736918 single base substitution G A intron_variant MELA-AU 7 72736971 72736971 single base substitution G A intron_variant MELA-AU 7 72737165 72737165 single base substitution G A intron_variant MELA-AU 7 72737224 72737224 single base substitution C T intron_variant MELA-AU 7 72737317 72737317 single base substitution G A intron_variant MELA-AU 7 72737382 72737382 single base substitution T C intron_variant MELA-AU 7 72737687 72737687 single base substitution G A intron_variant MELA-AU 7 72737760 72737760 single base substitution C A intron_variant MELA-AU 7 72737971 72737971 single base substitution G A intron_variant MELA-AU 7 72738320 72738320 single base substitution G A intron_variant MELA-AU 7 72739392 72739392 single base substitution C T intron_variant MELA-AU 7 72739689 72739689 single base substitution C T intron_variant MELA-AU 7 72739689 72739689 single base substitution C T upstream_gene_variant MELA-AU 7 72739738 72739738 single base substitution G A intron_variant MELA-AU 7 72739738 72739738 single base substitution G A upstream_gene_variant MELA-AU 7 72739828 72739828 single base substitution G A intron_variant MELA-AU 7 72739828 72739828 single base substitution G A upstream_gene_variant MELA-AU 7 72739893 72739893 single base substitution G A intron_variant MELA-AU 7 72739893 72739893 single base substitution G A upstream_gene_variant MELA-AU 7 72740027 72740027 single base substitution G A intron_variant MELA-AU 7 72740027 72740027 single base substitution G A upstream_gene_variant MELA-AU 7 72740102 72740102 single base substitution C T intron_variant MELA-AU 7 72740102 72740102 single base substitution C T upstream_gene_variant MELA-AU 7 72740162 72740162 single base substitution G A intron_variant MELA-AU 7 72740162 72740162 single base substitution G A upstream_gene_variant MELA-AU 7 72740255 72740255 single base substitution T A intron_variant MELA-AU 7 72740255 72740255 single base substitution T A upstream_gene_variant MELA-AU 7 72740336 72740336 single base substitution G A intron_variant MELA-AU 7 72740336 72740336 single base substitution G A upstream_gene_variant MELA-AU 7 72740376 72740376 single base substitution G A intron_variant MELA-AU 7 72740376 72740376 single base substitution G A upstream_gene_variant MELA-AU 7 72740442 72740442 single base substitution C T intron_variant MELA-AU 7 72740442 72740442 single base substitution C T upstream_gene_variant MELA-AU 7 72740575 72740575 single base substitution C T intron_variant MELA-AU 7 72740575 72740575 single base substitution C T upstream_gene_variant MELA-AU 7 72740605 72740605 single base substitution A G intron_variant MELA-AU 7 72740605 72740605 single base substitution A G upstream_gene_variant MELA-AU 7 72740725 72740725 single base substitution G A intron_variant MELA-AU 7 72740725 72740725 single base substitution G A upstream_gene_variant MELA-AU 7 72740901 72740901 single base substitution T A intron_variant MELA-AU 7 72740901 72740901 single base substitution T A upstream_gene_variant MELA-AU 7 72741117 72741117 single base substitution T A intron_variant MELA-AU 7 72741117 72741117 single base substitution T A upstream_gene_variant MELA-AU 7 72741136 72741136 single base substitution T G intron_variant MELA-AU 7 72741136 72741136 single base substitution T G upstream_gene_variant MELA-AU 7 72741153 72741153 single base substitution C T intron_variant MELA-AU 7 72741153 72741153 single base substitution C T upstream_gene_variant MELA-AU 7 72741401 72741401 single base substitution G A intron_variant MELA-AU 7 72741401 72741401 single base substitution G A upstream_gene_variant MELA-AU 7 72741563 72741565 deletion of <=200bp AAG - intron_variant MELA-AU 7 72741563 72741565 deletion of <=200bp AAG - upstream_gene_variant MELA-AU 7 72741812 72741812 single base substitution C T intron_variant MELA-AU 7 72741812 72741812 single base substitution C T upstream_gene_variant MELA-AU 7 72741830 72741830 single base substitution C T intron_variant MELA-AU 7 72741830 72741830 single base substitution C T upstream_gene_variant MELA-AU 7 72741876 72741876 single base substitution C T intron_variant MELA-AU 7 72741876 72741876 single base substitution C T upstream_gene_variant MELA-AU 7 72742190 72742190 single base substitution G A upstream_gene_variant MELA-AU 7 72742275 72742275 single base substitution G A upstream_gene_variant MELA-AU 7 72742293 72742293 single base substitution G A upstream_gene_variant MELA-AU 7 72742361 72742361 single base substitution G A upstream_gene_variant MELA-AU 7 72742687 72742687 single base substitution C T upstream_gene_variant MELA-AU 7 72742689 72742689 single base substitution G A upstream_gene_variant MELA-AU 7 72742720 72742720 single base substitution C T upstream_gene_variant MELA-AU 7 72742819 72742819 single base substitution T A upstream_gene_variant MELA-AU 7 72742943 72742943 single base substitution G A upstream_gene_variant MELA-AU 7 72743076 72743076 single base substitution G A upstream_gene_variant MELA-AU 7 72743404 72743404 single base substitution G A upstream_gene_variant MELA-AU 7 72743451 72743451 single base substitution G A upstream_gene_variant MELA-AU 7 72743580 72743580 single base substitution G A upstream_gene_variant MELA-AU 7 72743692 72743692 single base substitution T C upstream_gene_variant MELA-AU 7 72744286 72744286 single base substitution C T upstream_gene_variant MELA-AU 7 72744420 72744420 single base substitution T A upstream_gene_variant MELA-AU 7 72744462 72744462 single base substitution G A upstream_gene_variant MELA-AU 7 72744668 72744668 single base substitution G A upstream_gene_variant MELA-AU 7 72744939 72744939 single base substitution C T upstream_gene_variant MELA-AU 7 72744959 72744959 single base substitution C T upstream_gene_variant MELA-AU 7 72745044 72745044 single base substitution G A upstream_gene_variant MELA-AU 7 72745109 72745109 single base substitution G A upstream_gene_variant MELA-AU 7 72745325 72745325 single base substitution C T upstream_gene_variant MELA-AU 7 72745752 72745752 single base substitution C T upstream_gene_variant MELA-AU 7 72746242 72746242 single base substitution C T upstream_gene_variant MELA-AU 7 72746465 72746465 single base substitution C T upstream_gene_variant MELA-AU 7 72747007 72747007 single base substitution G A upstream_gene_variant ORCA-IN 7 72731466 72731466 single base substitution C T downstream_gene_variant ORCA-IN 7 72731466 72731466 single base substitution C T intron_variant ORCA-IN 7 72731466 72731466 single base substitution C T upstream_gene_variant ORCA-IN 7 72743403 72743403 single base substitution C A upstream_gene_variant OV-AU 7 72722090 72722090 single base substitution G C downstream_gene_variant OV-AU 7 72725710 72725710 single base substitution C G downstream_gene_variant OV-AU 7 72726045 72726045 single base substitution T G downstream_gene_variant OV-AU 7 72726555 72726555 single base substitution A G 3_prime_UTR_variant OV-AU 7 72726555 72726555 single base substitution A G downstream_gene_variant OV-AU 7 72726637 72726637 single base substitution G A 3_prime_UTR_variant OV-AU 7 72726637 72726637 single base substitution G A downstream_gene_variant OV-AU 7 72731654 72731654 single base substitution G T downstream_gene_variant OV-AU 7 72731654 72731654 single base substitution G T intron_variant OV-AU 7 72731654 72731654 single base substitution G T upstream_gene_variant OV-AU 7 72732550 72732550 single base substitution C A downstream_gene_variant OV-AU 7 72732550 72732550 single base substitution C A intron_variant OV-AU 7 72732550 72732550 single base substitution C A upstream_gene_variant OV-AU 7 72740432 72740432 single base substitution C G intron_variant OV-AU 7 72740432 72740432 single base substitution C G upstream_gene_variant OV-AU 7 72740627 72740627 single base substitution A C intron_variant OV-AU 7 72740627 72740627 single base substitution A C upstream_gene_variant PACA-AU 7 72722128 72722128 single base substitution T G downstream_gene_variant PACA-AU 7 72724197 72724197 single base substitution G A downstream_gene_variant PACA-AU 7 72726980 72726980 single base substitution G T downstream_gene_variant PACA-AU 7 72726980 72726980 single base substitution G T synonymous_variant P467P 1401C>A PACA-AU 7 72726989 72726989 single base substitution G A downstream_gene_variant PACA-AU 7 72726989 72726989 single base substitution G A synonymous_variant N464N 1392C>T PACA-AU 7 72727297 72727297 single base substitution G A downstream_gene_variant PACA-AU 7 72727297 72727297 single base substitution G A missense_variant R362C 1084C>T PACA-AU 7 72734441 72734441 single base substitution T C downstream_gene_variant PACA-AU 7 72734441 72734441 single base substitution T C intron_variant PACA-AU 7 72734441 72734441 single base substitution T C upstream_gene_variant PACA-AU 7 72736347 72736347 insertion of <=200bp - CAA intron_variant PACA-AU 7 72738201 72738201 single base substitution G T intron_variant PACA-AU 7 72738566 72738566 single base substitution C T exon_variant PACA-AU 7 72738566 72738566 single base substitution C T missense_variant V74M 220G>A PACA-AU 7 72739859 72739859 single base substitution A T intron_variant PACA-AU 7 72739859 72739859 single base substitution A T upstream_gene_variant PACA-AU 7 72740078 72740078 single base substitution G C intron_variant PACA-AU 7 72740078 72740078 single base substitution G C upstream_gene_variant PACA-AU 7 72741808 72741808 single base substitution G A intron_variant PACA-AU 7 72741808 72741808 single base substitution G A upstream_gene_variant PACA-AU 7 72742383 72742383 single base substitution C T upstream_gene_variant PACA-AU 7 72743509 72743509 single base substitution C T upstream_gene_variant PACA-AU 7 72745523 72745523 deletion of <=200bp T - upstream_gene_variant PACA-AU 7 72746603 72746603 single base substitution G A upstream_gene_variant PACA-CA 7 72726859 72726859 single base substitution G A 3_prime_UTR_variant PACA-CA 7 72726859 72726859 single base substitution G A downstream_gene_variant PACA-CA 7 72730479 72730479 single base substitution G C intron_variant PACA-CA 7 72731772 72731772 single base substitution C T downstream_gene_variant PACA-CA 7 72731772 72731772 single base substitution C T intron_variant PACA-CA 7 72731772 72731772 single base substitution C T upstream_gene_variant PACA-CA 7 72733729 72733729 single base substitution G T downstream_gene_variant PACA-CA 7 72733729 72733729 single base substitution G T intron_variant PACA-CA 7 72733729 72733729 single base substitution G T upstream_gene_variant PACA-CA 7 72733850 72733850 single base substitution A G downstream_gene_variant PACA-CA 7 72733850 72733850 single base substitution A G intron_variant PACA-CA 7 72733850 72733850 single base substitution A G upstream_gene_variant PACA-CA 7 72741148 72741148 single base substitution A T intron_variant PACA-CA 7 72741148 72741148 single base substitution A T upstream_gene_variant PACA-CA 7 72743817 72743817 single base substitution G T upstream_gene_variant PACA-CA 7 72744889 72744889 single base substitution G A upstream_gene_variant PACA-CA 7 72745498 72745498 single base substitution A G upstream_gene_variant PACA-CA 7 72746878 72746878 single base substitution T A upstream_gene_variant PAEN-AU 7 72737958 72737958 single base substitution C G intron_variant PAEN-IT 7 72729069 72729069 single base substitution G T intron_variant PBCA-DE 7 72742741 72742741 single base substitution C A upstream_gene_variant PBCA-DE 7 72745470 72745470 single base substitution C G upstream_gene_variant PRAD-CA 7 72746162 72746162 single base substitution C T upstream_gene_variant PRAD-UK 7 72733629 72733629 single base substitution G C downstream_gene_variant PRAD-UK 7 72733629 72733629 single base substitution G C intron_variant PRAD-UK 7 72733629 72733629 single base substitution G C upstream_gene_variant PRAD-UK 7 72733859 72733859 single base substitution G A downstream_gene_variant PRAD-UK 7 72733859 72733859 single base substitution G A intron_variant PRAD-UK 7 72733859 72733859 single base substitution G A upstream_gene_variant PRAD-UK 7 72739790 72739790 single base substitution C T intron_variant PRAD-UK 7 72739790 72739790 single base substitution C T upstream_gene_variant PRAD-UK 7 72741086 72741086 single base substitution G A intron_variant PRAD-UK 7 72741086 72741086 single base substitution G A upstream_gene_variant PRAD-UK 7 72741988 72741988 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PRAD-UK 7 72741988 72741988 single base substitution G A upstream_gene_variant PRAD-UK 7 72742085 72742085 single base substitution T A 5_prime_UTR_variant PRAD-UK 7 72742085 72742085 single base substitution T A upstream_gene_variant PRAD-UK 7 72742508 72742508 single base substitution G A upstream_gene_variant PRAD-US 7 72744195 72744195 single base substitution G A upstream_gene_variant READ-US 7 72727297 72727297 single base substitution G A downstream_gene_variant READ-US 7 72727297 72727297 single base substitution G A missense_variant R362C 1084C>T READ-US 7 72744195 72744195 single base substitution G A upstream_gene_variant RECA-EU 7 72729928 72729928 single base substitution G A intron_variant RECA-EU 7 72736663 72736663 single base substitution T G intron_variant RECA-EU 7 72743586 72743586 single base substitution C A upstream_gene_variant SKCA-BR 7 72724164 72724164 single base substitution C A downstream_gene_variant SKCA-BR 7 72724368 72724368 single base substitution G A downstream_gene_variant SKCA-BR 7 72724394 72724394 single base substitution A G downstream_gene_variant SKCA-BR 7 72724666 72724666 single base substitution C T downstream_gene_variant SKCA-BR 7 72725611 72725611 single base substitution T G downstream_gene_variant SKCA-BR 7 72726673 72726673 single base substitution C T 3_prime_UTR_variant SKCA-BR 7 72726673 72726673 single base substitution C T downstream_gene_variant SKCA-BR 7 72729978 72729978 single base substitution C T intron_variant SKCA-BR 7 72730558 72730558 single base substitution C T intron_variant SKCA-BR 7 72730558 72730558 single base substitution C T splice_region_variant SKCA-BR 7 72731008 72731008 single base substitution C T downstream_gene_variant SKCA-BR 7 72731008 72731008 single base substitution C T intron_variant SKCA-BR 7 72731008 72731008 single base substitution C T upstream_gene_variant SKCA-BR 7 72731623 72731623 single base substitution C T downstream_gene_variant SKCA-BR 7 72731623 72731623 single base substitution C T intron_variant SKCA-BR 7 72731623 72731623 single base substitution C T upstream_gene_variant SKCA-BR 7 72731664 72731664 single base substitution C T downstream_gene_variant SKCA-BR 7 72731664 72731664 single base substitution C T intron_variant SKCA-BR 7 72731664 72731664 single base substitution C T upstream_gene_variant SKCA-BR 7 72735655 72735655 single base substitution G A downstream_gene_variant SKCA-BR 7 72735655 72735655 single base substitution G A intron_variant SKCA-BR 7 72735655 72735655 single base substitution G A upstream_gene_variant SKCA-BR 7 72736220 72736220 single base substitution C G intron_variant SKCA-BR 7 72737316 72737316 single base substitution C T intron_variant SKCA-BR 7 72737601 72737601 single base substitution G A intron_variant SKCA-BR 7 72740408 72740408 insertion of <=200bp - CT intron_variant SKCA-BR 7 72740408 72740408 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 7 72740562 72740562 single base substitution T A intron_variant SKCA-BR 7 72740562 72740562 single base substitution T A upstream_gene_variant SKCA-BR 7 72742190 72742190 single base substitution G A upstream_gene_variant SKCA-BR 7 72745793 72745793 single base substitution G C upstream_gene_variant SKCA-BR 7 72746191 72746191 single base substitution C T upstream_gene_variant SKCA-BR 7 72746441 72746441 single base substitution G A upstream_gene_variant SKCM-US 7 72727133 72727133 single base substitution G A downstream_gene_variant SKCM-US 7 72727133 72727133 single base substitution G A synonymous_variant L416L 1248C>T SKCM-US 7 72730583 72730583 single base substitution G A exon_variant SKCM-US 7 72730583 72730583 single base substitution G A synonymous_variant L285L 855C>T SKCM-US 7 72732989 72732989 single base substitution C T downstream_gene_variant SKCM-US 7 72732989 72732989 single base substitution C T synonymous_variant V186V 558G>A SKCM-US 7 72732989 72732989 single base substitution C T upstream_gene_variant SKCM-US 7 72738546 72738546 single base substitution G A exon_variant SKCM-US 7 72738546 72738546 single base substitution G A synonymous_variant L80L 240C>T SKCM-US 7 72738612 72738612 single base substitution C T exon_variant SKCM-US 7 72738612 72738612 single base substitution C T synonymous_variant Q58Q 174G>A SKCM-US 7 72738661 72738661 single base substitution G A exon_variant SKCM-US 7 72738661 72738661 single base substitution G A missense_variant S42F 125C>T SKCM-US 7 72742623 72742623 single base substitution G A upstream_gene_variant SKCM-US 7 72743404 72743404 single base substitution G A upstream_gene_variant SKCM-US 7 72743439 72743439 single base substitution G A upstream_gene_variant SKCM-US 7 72743446 72743446 single base substitution G A upstream_gene_variant SKCM-US 7 72744229 72744229 single base substitution G A upstream_gene_variant SKCM-US 7 72744236 72744236 single base substitution G A upstream_gene_variant SKCM-US 7 72744286 72744286 single base substitution C T upstream_gene_variant SKCM-US 7 72745659 72745659 single base substitution G A upstream_gene_variant SKCM-US 7 72745679 72745679 single base substitution C T upstream_gene_variant SKCM-US 7 72745695 72745695 single base substitution G A upstream_gene_variant SKCM-US 7 72745747 72745747 single base substitution C T upstream_gene_variant STAD-US 7 72722449 72722451 deletion of <=200bp CTT - downstream_gene_variant STAD-US 7 72722714 72722714 single base substitution A G downstream_gene_variant STAD-US 7 72722781 72722781 single base substitution G A downstream_gene_variant STAD-US 7 72727084 72727084 single base substitution G A downstream_gene_variant STAD-US 7 72727084 72727084 single base substitution G A missense_variant P433S 1297C>T STAD-US 7 72732951 72732951 deletion of <=200bp C - downstream_gene_variant STAD-US 7 72732951 72732951 deletion of <=200bp C - frameshift_variant G199 STAD-US 7 72732951 72732951 deletion of <=200bp C - upstream_gene_variant STAD-US 7 72734221 72734221 single base substitution G T downstream_gene_variant STAD-US 7 72734221 72734221 single base substitution G T synonymous_variant I140I 420C>A STAD-US 7 72734221 72734221 single base substitution G T upstream_gene_variant STAD-US 7 72738518 72738518 single base substitution C T exon_variant STAD-US 7 72738518 72738518 single base substitution C T missense_variant V90M 268G>A STAD-US 7 72738631 72738631 single base substitution C T exon_variant STAD-US 7 72738631 72738631 single base substitution C T missense_variant R52H 155G>A THCA-SA 7 72730672 72730672 single base substitution C T exon_variant THCA-SA 7 72730672 72730672 single base substitution C T missense_variant A256T 766G>A UCEC-US 7 72727001 72727001 single base substitution C T downstream_gene_variant UCEC-US 7 72727001 72727001 single base substitution C T synonymous_variant E460E 1380G>A UCEC-US 7 72727296 72727296 single base substitution C T downstream_gene_variant UCEC-US 7 72727296 72727296 single base substitution C T missense_variant R362H 1085G>A UCEC-US 7 72727474 72727474 single base substitution C T exon_variant UCEC-US 7 72727474 72727474 single base substitution C T missense_variant A303T 907G>A UCEC-US 7 72738453 72738453 single base substitution G A exon_variant UCEC-US 7 72738453 72738453 single base substitution G A synonymous_variant C111C 333C>T UCEC-US 7 72743397 72743397 single base substitution A C upstream_gene_variant UCEC-US 7 72743470 72743470 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 ESCC_114 COSM3086962 c.554T>C p.L185P Substitution - Missense 7:73318994-73318994 - TCGA-A2-A25E-01 COSM3833161 c.1269C>A p.G423G Substitution - coding silent 7:73313116-73313116 - T3255 COSM1091533 c.1077C>T p.S359S Substitution - coding silent 7:73313308-73313308 - Pat_60_B COSM5873024 c.163G>A p.V55M Substitution - Missense 7:73324625-73324625 - TCGA-A6-6782-01 COSM1451946 c.549C>T p.H183H Substitution - coding silent 7:73318999-73318999 - TCGA-D5-6927-01 COSM5165198 c.332G>A p.C111Y Substitution - Missense 7:73324456-73324456 - CAL27 COSM4162401 c.37T>C p.W13R Substitution - Missense BICR_22 COSM4162401 c.37T>C p.W13R Substitution - Missense Pat_50_A COSM5873021 c.1300G>A p.D434N Substitution - Missense 7:73313085-73313085 - 5 COSM4333394 c.716A>T p.K239M Substitution - Missense 7:73318832-73318832 - TCGA-26-5136 COSM2157131 c.482G>A p.R161Q Substitution - Missense 7:73320160-73320160 - 8047896 COSM3394873 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - B109 COSM1755346 c.336T>G p.G112G Substitution - coding silent 7:73324452-73324452 - TCGA-BR-8361-01 COSM3882213 c.1297C>T p.P433S Substitution - Missense 7:73313088-73313088 - CSCC-16-T COSM4515674 c.1244_1245GG>AA p.G415E Substitution - Missense 7:73313140-73313141 - CSCC-52-T COSM4462422 c.1246C>T p.L416F Substitution - Missense 7:73313139-73313139 - WSU-HN13 COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-22-5473-01 COSM747195 c.677A>T p.E226V Substitution - Missense 7:73318871-73318871 - TCGA-13-2057-01 COSM1330539 c.1115G>A p.R372H Substitution - Missense 7:73313270-73313270 - UPCI:SCC090 COSM4162404 c.23T>C p.L8P Substitution - Missense 30996 COSM5044246 c.858C>A p.F286L Substitution - Missense 7:73316581-73316581 - PTC-7C COSM4162405 c.23T>C p.L8P Substitution - Missense TCGA-AN-A046-01 COSM235511 c.696C>T p.F232F Substitution - coding silent 7:73318852-73318852 - TCGA-D5-6932-01 COSM1451941 c.1243G>A p.G415R Substitution - Missense 7:73313142-73313142 - J76_T COSM3950753 c.1196C>T p.A399V Substitution - Missense 7:73313189-73313189 - PD23567a COSM3086982 c.225C>T p.I75I Substitution - coding silent 7:73324563-73324563 - CSCC-49-T COSM4549839 c.483G>A p.R161R Substitution - coding silent 7:73320159-73320159 - TCGA-AZ-4313-01 COSM5138996 c.532G>A p.E178K Substitution - Missense 7:73319016-73319016 - TCGA-B5-A0JY-01 COSM1091532 c.1085G>A p.R362H Substitution - Missense 7:73313300-73313300 - TCGA-AG-A002-01 COSM235510 c.696C>T p.F232F Substitution - coding silent 7:73318852-73318852 - WSU-HN30 COSM4162401 c.37T>C p.W13R Substitution - Missense B59-1-Tumor COSM4006754 c.179T>G p.V60G Substitution - Missense 7:73324609-73324609 - CLL047 COSM1292536 c.297C>T p.F99F Substitution - coding silent 7:73324491-73324491 - 2296_T COSM3950758 c.444A>G p.K148K Substitution - coding silent 7:73320198-73320198 - CRC-14T COSM5452169 c.48T>C p.C16C Substitution - coding silent 7:73324740-73324740 - SCC-25 COSM4162405 c.23T>C p.L8P Substitution - Missense TCGA-D5-6922-01 COSM1451939 c.1422C>T p.S474S Substitution - coding silent 7:73312963-73312963 - TCGA-BS-A0UL-01 COSM1091537 c.333C>T p.C111C Substitution - coding silent 7:73324455-73324455 - TCGA-66-2781-01 COSM747201 c.1272A>C p.E424D Substitution - Missense 7:73313113-73313113 - TCGA-FD-A3SN-01 COSM3778559 c.154C>T p.R52C Substitution - Missense 7:73324634-73324634 - TCGA-CG-5727-01 COSM3882216 c.420C>A p.I140I Substitution - coding silent 7:73320222-73320222 - Detroit_562 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-B5-A0JY-01 COSM1091531 c.1085G>A p.R362H Substitution - Missense 7:73313300-73313300 - 587246 COSM1230354 c.1043G>A p.R348H Substitution - Missense 7:73313342-73313342 - TCGA-CG-5727-01 COSM3882215 c.420C>A p.I140I Substitution - coding silent 7:73320222-73320222 - BHY COSM4162404 c.23T>C p.L8P Substitution - Missense BICR_22 COSM4162400 c.37T>C p.W13R Substitution - Missense pfg282T COSM4757339 c.958C>T p.L320F Substitution - Missense 7:73313427-73313427 - TCGA-EE-A2MR-06 COSM3640305 c.240C>T p.L80L Substitution - coding silent 7:73324548-73324548 - CSCC-49-T COSM4549840 c.483G>A p.R161R Substitution - coding silent 7:73320159-73320159 - CSCC-31-T COSM4469392 c.159C>T p.C53C Substitution - coding silent 7:73324629-73324629 - TCGA-AA-3663-01 COSM3698529 c.942G>A p.T314T Substitution - coding silent 7:73313443-73313443 - UM-SCC-47 COSM4162400 c.37T>C p.W13R Substitution - Missense C086 COSM5540819 c.1024C>T p.R342C Substitution - Missense 7:73313361-73313361 - TCGA-D5-6927-01 COSM5165197 c.332G>A p.C111Y Substitution - Missense 7:73324456-73324456 - LUAD-NYU408 COSM374574 c.218G>T p.R73M Substitution - Missense 7:73324570-73324570 - CSCC-20-T COSM4450631 c.739_749+14del25 p.? Unknown 7:73318673-73318697 - T2258 COSM4736136 c.660G>A p.E220E Substitution - coding silent 7:73318888-73318888 - 93VU147T COSM4162405 c.23T>C p.L8P Substitution - Missense tumor_4184094 COSM3358159 c.234G>A p.L78L Substitution - coding silent 7:73324554-73324554 - UD-SCC-2 COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-BS-A0U7-01 COSM1091533 c.1077C>T p.S359S Substitution - coding silent 7:73313308-73313308 - MDA-MB-435 COSM1673207 c.1174G>A p.G392S Substitution - Missense 7:73313211-73313211 - REC-1 COSM323992 c.841G>A p.V281M Substitution - Missense 7:73316598-73316598 - TCGA-A2-A25E-01 COSM3833162 c.1269C>A p.G423G Substitution - coding silent 7:73313116-73313116 - SCC-9 COSM4162405 c.23T>C p.L8P Substitution - Missense SCC-15 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-EE-A2MD-06 COSM3640303 c.558G>A p.V186V Substitution - coding silent 7:73318990-73318990 - TCGA-AZ-6608-01 COSM5143393 c.1314G>A p.P438P Substitution - coding silent 7:73313071-73313071 - pfg008T COSM4757338 c.1301A>G p.D434G Substitution - Missense 7:73313084-73313084 - ESO-0025 COSM1268553 c.991C>A p.R331S Substitution - Missense 7:73313394-73313394 - PT13 COSM5895929 c.667G>A p.A223T Substitution - Missense 7:73318881-73318881 - PTC_441 COSM5957296 c.766G>A p.A256T Substitution - Missense 7:73316673-73316673 - WSU-HN12 COSM4162405 c.23T>C p.L8P Substitution - Missense ESO-717 COSM1242954 c.495+1G>A p.? Unknown 7:73320146-73320146 - CSCC-44-T COSM4463964 c.1312C>T p.P438S Substitution - Missense 7:73313073-73313073 - CRC-14T COSM5452170 c.48T>C p.C16C Substitution - coding silent 7:73324740-73324740 - PTC-7C COSM4162403 c.24G>A p.L8L Substitution - coding silent TCGA-CG-5728-01 COSM3882218 c.268G>A p.V90M Substitution - Missense 7:73324520-73324520 - XHDG38 COSM4769782 c.1237C>T p.R413C Substitution - Missense 7:73313148-73313148 - PTC-7C COSM4162402 c.24G>A p.L8L Substitution - coding silent CSCC-11-T COSM4491322 c.378C>T p.S126S Substitution - coding silent 7:73324410-73324410 - UM-SCC-4 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-NH-A8F7-06 COSM3882218 c.268G>A p.V90M Substitution - Missense 7:73324520-73324520 - CSCC-27-T COSM4502644 c.618C>T p.A206A Substitution - coding silent 7:73318930-73318930 - UM-SCC-17B COSM4162400 c.37T>C p.W13R Substitution - Missense ESO-0025 COSM1268554 c.991C>A p.R331S Substitution - Missense 7:73313394-73313394 - CSCC-31-T COSM4469391 c.159C>T p.C53C Substitution - coding silent 7:73324629-73324629 - XHDG38 COSM4769781 c.1237C>T p.R413C Substitution - Missense 7:73313148-73313148 - BHY COSM4162401 c.37T>C p.W13R Substitution - Missense UM-SCC-11B COSM4162404 c.23T>C p.L8P Substitution - Missense UM-SCC-4 COSM4162400 c.37T>C p.W13R Substitution - Missense B59-1-Tumor COSM4006755 c.179T>G p.V60G Substitution - Missense 7:73324609-73324609 - TCGA-FU-A5XV-01 COSM4844261 c.691C>T p.Q231* Substitution - Nonsense 7:73318857-73318857 - TCGA-BS-A0U7-01 COSM1091534 c.1077C>T p.S359S Substitution - coding silent 7:73313308-73313308 - ESO-669 COSM1268556 c.838A>T p.T280S Substitution - Missense 7:73316601-73316601 - TCGA-CZ-5461-01 COSM485531 c.728A>T p.K243M Substitution - Missense 7:73318708-73318708 - TCGA-21-1076-01 COSM747194 c.422C>A p.S141Y Substitution - Missense 7:73320220-73320220 - TCGA-26-5136-01 COSM2157132 c.482G>A p.R161Q Substitution - Missense 7:73320160-73320160 - TCGA-BR-4370-01 COSM3882219 c.155G>A p.R52H Substitution - Missense 7:73324633-73324633 - CHC892T COSM4958872 c.1355C>T p.P452L Substitution - Missense 7:73313030-73313030 - UM-SCC-17B COSM4162401 c.37T>C p.W13R Substitution - Missense CSCC-7-T COSM4520614 c.1067G>A p.G356D Substitution - Missense 7:73313318-73313318 - WSU-HN30 COSM4162404 c.23T>C p.L8P Substitution - Missense UM-SCC-11B COSM4162400 c.37T>C p.W13R Substitution - Missense 4537_T COSM3950757 c.466A>G p.K156E Substitution - Missense 7:73320176-73320176 - TCGA-BH-A0B6-01 COSM3833164 c.381C>T p.T127T Substitution - coding silent 7:73324407-73324407 - CAL27 COSM4162405 c.23T>C p.L8P Substitution - Missense UM-SCC-47 COSM4162405 c.23T>C p.L8P Substitution - Missense CSCC-7-T COSM293099 c.676G>A p.E226K Substitution - Missense 7:73318872-73318872 - TCGA-AA-3663-01 COSM3698528 c.942G>A p.T314T Substitution - coding silent 7:73313443-73313443 - TCGA-EE-A3JH-06 COSM3640301 c.855C>T p.L285L Substitution - coding silent 7:73316584-73316584 - sysucc-1370T COSM5472436 c.1012G>A p.V338I Substitution - Missense 7:73313373-73313373 - PD23567a COSM3086981 c.225C>T p.I75I Substitution - coding silent 7:73324563-73324563 - B109-Tumor COSM1755347 c.336T>G p.G112G Substitution - coding silent 7:73324452-73324452 - 8036161 COSM3394872 c.1392C>T p.N464N Substitution - coding silent 7:73312993-73312993 - T2258 COSM4736137 c.660G>A p.E220E Substitution - coding silent 7:73318888-73318888 - TCGA-EE-A3JD-06 COSM4393975 c.125C>T p.S42F Substitution - Missense 7:73324663-73324663 - B109 COSM1755347 c.336T>G p.G112G Substitution - coding silent 7:73324452-73324452 - TCGA-AP-A0LM-01 COSM1091530 c.1380G>A p.E460E Substitution - coding silent 7:73313005-73313005 - T3255 COSM1091534 c.1077C>T p.S359S Substitution - coding silent 7:73313308-73313308 - BHY COSM4162400 c.37T>C p.W13R Substitution - Missense TCGA-AZ-6608-01 COSM5143392 c.1314G>A p.P438P Substitution - coding silent 7:73313071-73313071 - 22T COSM108415 c.858C>T p.F286F Substitution - coding silent 7:73316581-73316581 - T3090 COSM4736141 c.78C>A p.P26P Substitution - coding silent 7:73324710-73324710 - TCGA-AA-3510-01 COSM1451944 c.997G>A p.D333N Substitution - Missense 7:73313388-73313388 - BCM791T COSM4803034 c.157T>C p.C53R Substitution - Missense 7:73324631-73324631 - 2492730 COSM5728796 c.1173G>A p.E391E Substitution - coding silent 7:73313212-73313212 - WSU-HN6 COSM4162405 c.23T>C p.L8P Substitution - Missense CAL33 COSM4162405 c.23T>C p.L8P Substitution - Missense 2250185 COSM5029404 c.765G>A p.Q255Q Substitution - coding silent 7:73316674-73316674 - UM-SCC-2 COSM4162401 c.37T>C p.W13R Substitution - Missense T3090 COSM4736140 c.78C>A p.P26P Substitution - coding silent 7:73324710-73324710 - TCGA-AZ-6601-01 COSM1451942 c.1038C>T p.C346C Substitution - coding silent 7:73313347-73313347 - 8036161 COSM3394869 c.1401C>A p.P467P Substitution - coding silent 7:73312984-73312984 - STC252 COSM5062554 c.736T>G p.S246A Substitution - Missense 7:73318700-73318700 - BHY COSM4162405 c.23T>C p.L8P Substitution - Missense TCGA-D5-6922-01 COSM1451938 c.1422C>T p.S474S Substitution - coding silent 7:73312963-73312963 - CSCC-52-T COSM4462423 c.1246C>T p.L416F Substitution - Missense 7:73313139-73313139 - CAL27 COSM4162400 c.37T>C p.W13R Substitution - Missense TCGA-AZ-4313-01 COSM5138997 c.532G>A p.E178K Substitution - Missense 7:73319016-73319016 - BCM791T COSM4803033 c.157T>C p.C53R Substitution - Missense 7:73324631-73324631 - CSCC-15-T COSM4469630 c.160C>T p.P54S Substitution - Missense 7:73324628-73324628 - 4537_T COSM3950756 c.466A>G p.K156E Substitution - Missense 7:73320176-73320176 - PTC-28C COSM4162398 c.1159A>G p.I387V Substitution - Missense 7:73313226-73313226 - 631052 COSM323992 c.841G>A p.V281M Substitution - Missense 7:73316598-73316598 - TCGA-FD-A3SN-01 COSM3778558 c.154C>T p.R52C Substitution - Missense 7:73324634-73324634 - TCGA-AM-5821-01 COSM3762817 c.225C>A p.I75I Substitution - coding silent 7:73324563-73324563 - T2969 COSM4736134 c.1056G>A p.E352E Substitution - coding silent 7:73313329-73313329 - 93VU147T COSM4162400 c.37T>C p.W13R Substitution - Missense J9_T COSM3950761 c.118C>G p.L40V Substitution - Missense 7:73324670-73324670 - TCGA-CG-5728-01 COSM3882217 c.268G>A p.V90M Substitution - Missense 7:73324520-73324520 - STC252 COSM5062556 c.221T>C p.V74A Substitution - Missense 7:73324567-73324567 - CAL27 COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-22-5473-01 COSM747196 c.677A>T p.E226V Substitution - Missense 7:73318871-73318871 - ORL-48 COSM4162405 c.23T>C p.L8P Substitution - Missense S01494 COSM316160 c.186C>T p.G62G Substitution - coding silent 7:73324602-73324602 - LAU63 COSM235511 c.696C>T p.F232F Substitution - coding silent 7:73318852-73318852 - ESCC_139 COSM5643278 c.121G>T p.V41F Substitution - Missense 7:73324667-73324667 - BICR_22 COSM4162405 c.23T>C p.L8P Substitution - Missense 2296_T COSM3950759 c.444A>G p.K148K Substitution - coding silent 7:73320198-73320198 - SCC-9 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-A2-A0T5-01 COSM3833165 c.350A>C p.H117P Substitution - Missense 7:73324438-73324438 - 631052 COSM323993 c.841G>A p.V281M Substitution - Missense 7:73316598-73316598 - TCGA-A6-6781-01 COSM5094548 c.1430G>C p.G477A Substitution - Missense 7:73312955-73312955 - UM-SCC-47 COSM4162401 c.37T>C p.W13R Substitution - Missense ESO-669 COSM1268555 c.838A>T p.T280S Substitution - Missense 7:73316601-73316601 - TCGA-AA-3681-01 COSM293099 c.676G>A p.E226K Substitution - Missense 7:73318872-73318872 - 2250185 COSM5029403 c.765G>A p.Q255Q Substitution - coding silent 7:73316674-73316674 - TCGA-BH-A0B6-01 COSM3833163 c.381C>T p.T127T Substitution - coding silent 7:73324407-73324407 - BCM791T COSM4803033 c.157T>C p.C53R Substitution - Missense 7:73324631-73324631 - CSCC-7-T COSM293098 c.676G>A p.E226K Substitution - Missense 7:73318872-73318872 - WSU-HN6 COSM4162400 c.37T>C p.W13R Substitution - Missense sysucc-1171T COSM1451942 c.1038C>T p.C346C Substitution - coding silent 7:73313347-73313347 - 587338 COSM1230352 c.941C>T p.T314M Substitution - Missense 7:73313444-73313444 - TCGA-EE-A3JH-06 COSM3640302 c.855C>T p.L285L Substitution - coding silent 7:73316584-73316584 - PTC_441 COSM5957295 c.766G>A p.A256T Substitution - Missense 7:73316673-73316673 - CSCC-37-T COSM4459811 c.1140C>T p.P380P Substitution - coding silent 7:73313245-73313245 - PTC-7C COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-CA-6717-01 COSM3698527 c.1394C>T p.S465L Substitution - Missense 7:73312991-73312991 - ESO-717 COSM1242955 c.495+1G>A p.? Unknown 7:73320146-73320146 - CSCC-11-T COSM4491321 c.378C>T p.S126S Substitution - coding silent 7:73324410-73324410 - TCGA-A6-6781-01 COSM5094549 c.1430G>C p.G477A Substitution - Missense 7:73312955-73312955 - pfg008T COSM4757337 c.1301A>G p.D434G Substitution - Missense 7:73313084-73313084 - TCGA-G4-6588-01 COSM5179251 c.1001A>G p.Y334C Substitution - Missense 7:73313384-73313384 - UM-SCC-47 COSM4162404 c.23T>C p.L8P Substitution - Missense sysucc-1370T COSM5472437 c.1012G>A p.V338I Substitution - Missense 7:73313373-73313373 - STC252 COSM5062557 c.221T>C p.V74A Substitution - Missense 7:73324567-73324567 - CSCC-20-T COSM4450630 c.739_749+14del25 p.? Unknown 7:73318673-73318697 - 6115115 COSM3394874 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - REC-1 COSM323993 c.841G>A p.V281M Substitution - Missense 7:73316598-73316598 - sysucc-1171T COSM1451943 c.1038C>T p.C346C Substitution - coding silent 7:73313347-73313347 - J9_T COSM3950760 c.118C>G p.L40V Substitution - Missense 7:73324670-73324670 - sysucc-1247T COSM5764556 c.1185C>T p.Y395Y Substitution - coding silent 7:73313200-73313200 - TCGA-EE-A29D-06 COSM3640299 c.1248C>T p.L416L Substitution - coding silent 7:73313137-73313137 - J30_T COSM3950755 c.1078G>T p.D360Y Substitution - Missense 7:73313307-73313307 - WSU-HN8 COSM4162401 c.37T>C p.W13R Substitution - Missense Detroit_562 COSM4162400 c.37T>C p.W13R Substitution - Missense tumor_4184094 COSM3358158 c.234G>A p.L78L Substitution - coding silent 7:73324554-73324554 - TCGA-BS-A0UL-01 COSM1091538 c.333C>T p.C111C Substitution - coding silent 7:73324455-73324455 - PTC-7C COSM4162400 c.37T>C p.W13R Substitution - Missense CAL33 COSM4162401 c.37T>C p.W13R Substitution - Missense 8047896 COSM3394874 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - C086 COSM5540818 c.1024C>T p.R342C Substitution - Missense 7:73313361-73313361 - D28 COSM5546024 c.555G>A p.L185L Substitution - coding silent 7:73318993-73318993 - 8067211 COSM3785761 c.220G>A p.V74M Substitution - Missense 7:73324568-73324568 - UM-SCC-4 COSM4162404 c.23T>C p.L8P Substitution - Missense 93VU147T COSM4162401 c.37T>C p.W13R Substitution - Missense LUAD-NYU408 COSM374573 c.218G>T p.R73M Substitution - Missense 7:73324570-73324570 - TCGA-26-5136 COSM2157132 c.482G>A p.R161Q Substitution - Missense 7:73320160-73320160 - CSCC-37-T COSM4459810 c.1140C>T p.P380P Substitution - coding silent 7:73313245-73313245 - UD-SCC-2 COSM4162400 c.37T>C p.W13R Substitution - Missense SCC-9 COSM4162404 c.23T>C p.L8P Substitution - Missense ORL-48 COSM4162400 c.37T>C p.W13R Substitution - Missense CAL33 COSM4162400 c.37T>C p.W13R Substitution - Missense CSCC-15-T COSM4469629 c.160C>T p.P54S Substitution - Missense 7:73324628-73324628 - WSU-HN12 COSM4162404 c.23T>C p.L8P Substitution - Missense WSU-HN30 COSM4162400 c.37T>C p.W13R Substitution - Missense CSCC-7-T COSM4520615 c.1067G>A p.G356D Substitution - Missense 7:73313318-73313318 - pfg282T COSM4757340 c.958C>T p.L320F Substitution - Missense 7:73313427-73313427 - 2492730 COSM5728795 c.1173G>A p.E391E Substitution - coding silent 7:73313212-73313212 - WSU-HN12 COSM4162400 c.37T>C p.W13R Substitution - Missense pfg181T COSM4757341 c.784G>A p.A262T Substitution - Missense 7:73316655-73316655 - NOKSI COSM4162401 c.37T>C p.W13R Substitution - Missense WSU-HN12 COSM4162401 c.37T>C p.W13R Substitution - Missense CHC892T COSM4958872 c.1355C>T p.P452L Substitution - Missense 7:73313030-73313030 - TCGA-BS-A0TJ-01 COSM1091535 c.907G>A p.A303T Substitution - Missense 7:73313478-73313478 - BCM791T COSM4803034 c.157T>C p.C53R Substitution - Missense 7:73324631-73324631 - 30996 COSM5044245 c.858C>A p.F286L Substitution - Missense 7:73316581-73316581 - TCGA-FW-A3R5-06 COSM3923911 c.174G>A p.Q58Q Substitution - coding silent 7:73324614-73324614 - TCGA-BH-A0HA-01 COSM453337 c.806_807insA p.P270fs*7 Insertion - Frameshift 7:73316632-73316633 - TCGA-26-5136-01 COSM2157131 c.482G>A p.R161Q Substitution - Missense 7:73320160-73320160 - SCC-15 COSM4162404 c.23T>C p.L8P Substitution - Missense UM-SCC-2 COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-BR-8361-01 COSM3882214 c.1297C>T p.P433S Substitution - Missense 7:73313088-73313088 - UM-SCC-2 COSM4162405 c.23T>C p.L8P Substitution - Missense Detroit_562 COSM4162405 c.23T>C p.L8P Substitution - Missense TCGA-AG-3592-01 COSM3394873 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - TCGA-AP-A0LM-01 COSM1091529 c.1380G>A p.E460E Substitution - coding silent 7:73313005-73313005 - S02322 COSM5691553 c.386A>G p.Y129C Substitution - Missense 7:73324402-73324402 - CHC892T COSM4958871 c.1355C>T p.P452L Substitution - Missense 7:73313030-73313030 - UD-SCC-2 COSM4162405 c.23T>C p.L8P Substitution - Missense STC252 COSM5062555 c.736T>G p.S246A Substitution - Missense 7:73318700-73318700 - TCGA-AG-A002-01 COSM235511 c.696C>T p.F232F Substitution - coding silent 7:73318852-73318852 - T3498 COSM4736139 c.241C>T p.P81S Substitution - Missense 7:73324547-73324547 - sysucc-1247T COSM5764557 c.1185C>T p.Y395Y Substitution - coding silent 7:73313200-73313200 - TCGA-CA-6717-01 COSM3698526 c.1394C>T p.S465L Substitution - Missense 7:73312991-73312991 - TCGA-BH-A0HA-01 COSM453338 c.806_807insA p.P270fs*7 Insertion - Frameshift 7:73316632-73316633 - ORL-48 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-D5-6932-01 COSM1451940 c.1243G>A p.G415R Substitution - Missense 7:73313142-73313142 - J76_T COSM3950752 c.1196C>T p.A399V Substitution - Missense 7:73313189-73313189 - WSU-HN6 COSM4162404 c.23T>C p.L8P Substitution - Missense SCC-25 COSM4162400 c.37T>C p.W13R Substitution - Missense UM-SCC-17B COSM4162405 c.23T>C p.L8P Substitution - Missense YUSWI COSM1698738 c.1285G>A p.D429N Substitution - Missense 7:73313100-73313100 - NOKSI COSM4162405 c.23T>C p.L8P Substitution - Missense TCGA-BR-4370-01 COSM3882220 c.155G>A p.R52H Substitution - Missense 7:73324633-73324633 - TCGA-FU-A5XV-01 COSM4844260 c.691C>T p.Q231* Substitution - Nonsense 7:73318857-73318857 - PTC-7C COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-AA-3681-01 COSM293098 c.676G>A p.E226K Substitution - Missense 7:73318872-73318872 - S01494 COSM316160 c.186C>T p.G62G Substitution - coding silent 7:73324602-73324602 - TCGA-EE-A2MR-06 COSM3640306 c.240C>T p.L80L Substitution - coding silent 7:73324548-73324548 - Detroit_562 COSM4162403 c.24G>A p.L8L Substitution - coding silent SCC-15 COSM4162405 c.23T>C p.L8P Substitution - Missense SCC-25 COSM4162401 c.37T>C p.W13R Substitution - Missense UPCI:SCC090 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-AA-3510-01 COSM1451945 c.997G>A p.D333N Substitution - Missense 7:73313388-73313388 - 93VU147T COSM4162404 c.23T>C p.L8P Substitution - Missense XHDG25 COSM4769085 c.1296C>T p.R432R Substitution - coding silent 7:73313089-73313089 - NOKSI COSM4162400 c.37T>C p.W13R Substitution - Missense D28 COSM5546023 c.555G>A p.L185L Substitution - coding silent 7:73318993-73318993 - S01494 COSM316161 c.186C>T p.G62G Substitution - coding silent 7:73324602-73324602 - TCGA-66-2781-01 COSM747202 c.1272A>C p.E424D Substitution - Missense 7:73313113-73313113 - Detroit_562 COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-AN-A046-01 COSM235510 c.696C>T p.F232F Substitution - coding silent 7:73318852-73318852 - ESCC_114 COSM3086961 c.554T>C p.L185P Substitution - Missense 7:73318994-73318994 - PT13 COSM5895930 c.667G>A p.A223T Substitution - Missense 7:73318881-73318881 - 587246 COSM1230355 c.1043G>A p.R348H Substitution - Missense 7:73313342-73313342 - S01494 COSM316161 c.186C>T p.G62G Substitution - coding silent 7:73324602-73324602 - CSCC-16-T COSM4515673 c.1244_1245GG>AA p.G415E Substitution - Missense 7:73313140-73313141 - 8068577 COSM3394874 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - TCGA-NH-A8F7-06 COSM3882217 c.268G>A p.V90M Substitution - Missense 7:73324520-73324520 - TCGA-24-1422-01 COSM116677 c.1170G>C p.K390N Substitution - Missense 7:73313215-73313215 - TCGA-A6-6782-01 COSM1451947 c.549C>T p.H183H Substitution - coding silent 7:73318999-73318999 - 1_PRE-TREATMENT COSM1720773 c.446delA p.K149fs*10 Deletion - Frameshift 7:73320196-73320196 - CHC892T COSM4958871 c.1355C>T p.P452L Substitution - Missense 7:73313030-73313030 - TCGA-AM-5821-01 COSM3762816 c.225C>A p.I75I Substitution - coding silent 7:73324563-73324563 - SCC-25 COSM4162404 c.23T>C p.L8P Substitution - Missense Pat_50_A COSM5873022 c.1300G>A p.D434N Substitution - Missense 7:73313085-73313085 - WSU-HN6 COSM4162401 c.37T>C p.W13R Substitution - Missense 1_PRE-TREATMENT COSM1720774 c.446delA p.K149fs*10 Deletion - Frameshift 7:73320196-73320196 - PTC-28C COSM4162399 c.1159A>G p.I387V Substitution - Missense 7:73313226-73313226 - pfg181T COSM4757342 c.784G>A p.A262T Substitution - Missense 7:73316655-73316655 - ESCC_139 COSM5643277 c.121G>T p.V41F Substitution - Missense 7:73324667-73324667 - TCGA-13-2057-01 COSM1330538 c.1115G>A p.R372H Substitution - Missense 7:73313270-73313270 - TCGA-CZ-5461-01 COSM485530 c.728A>T p.K243M Substitution - Missense 7:73318708-73318708 - J30_T COSM3950754 c.1078G>T p.D360Y Substitution - Missense 7:73313307-73313307 - YUSWI COSM1698739 c.1285G>A p.D429N Substitution - Missense 7:73313100-73313100 - TCGA-EE-A2MD-06 COSM3640304 c.558G>A p.V186V Substitution - coding silent 7:73318990-73318990 - 8036161 COSM3394871 c.1392C>T p.N464N Substitution - coding silent 7:73312993-73312993 - TCGA-G4-6588-01 COSM5179252 c.1001A>G p.Y334C Substitution - Missense 7:73313384-73313384 - 8036161 COSM3394870 c.1401C>A p.P467P Substitution - coding silent 7:73312984-73312984 - UM-SCC-17B COSM4162404 c.23T>C p.L8P Substitution - Missense UPCI:SCC090 COSM4162400 c.37T>C p.W13R Substitution - Missense UM-SCC-2 COSM4162400 c.37T>C p.W13R Substitution - Missense CSCC-55-T COSM4498882 c.529C>T p.R177C Substitution - Missense 7:73319019-73319019 - TCGA-EE-A29D-06 COSM3640300 c.1248C>T p.L416L Substitution - coding silent 7:73313137-73313137 - TCGA-A2-A0T5-01 COSM3833166 c.350A>C p.H117P Substitution - Missense 7:73324438-73324438 - LAU63 COSM235510 c.696C>T p.F232F Substitution - coding silent 7:73318852-73318852 - 8067211 COSM3785760 c.220G>A p.V74M Substitution - Missense 7:73324568-73324568 - CSCC-44-T COSM4463965 c.1312C>T p.P438S Substitution - Missense 7:73313073-73313073 - UM-SCC-4 COSM4162405 c.23T>C p.L8P Substitution - Missense WSU-HN13 COSM4162401 c.37T>C p.W13R Substitution - Missense TCGA-AG-3592-01 COSM3394874 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - S02322 COSM5691552 c.386A>G p.Y129C Substitution - Missense 7:73324402-73324402 - WSU-HN8 COSM4162400 c.37T>C p.W13R Substitution - Missense CSCC-31-T COSM4560890 c.860G>T p.R287L Substitution - Missense 7:73316579-73316579 - 587338 COSM1230353 c.941C>T p.T314M Substitution - Missense 7:73313444-73313444 - Detroit_562 COSM4162402 c.24G>A p.L8L Substitution - coding silent NOKSI COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-21-1076-01 COSM747193 c.422C>A p.S141Y Substitution - Missense 7:73320220-73320220 - XHDG25 COSM4769084 c.1296C>T p.R432R Substitution - coding silent 7:73313089-73313089 - UPCI:SCC090 COSM4162405 c.23T>C p.L8P Substitution - Missense TCGA-BS-A0TJ-01 COSM1091536 c.907G>A p.A303T Substitution - Missense 7:73313478-73313478 - TCGA-AZ-6601-01 COSM1451943 c.1038C>T p.C346C Substitution - coding silent 7:73313347-73313347 - UM-SCC-11B COSM4162405 c.23T>C p.L8P Substitution - Missense WSU-HN30 COSM4162405 c.23T>C p.L8P Substitution - Missense YUGOE COSM1698740 c.846G>A p.W282* Substitution - Nonsense 7:73316593-73316593 - BICR_22 COSM4162404 c.23T>C p.L8P Substitution - Missense WSU-HN13 COSM4162405 c.23T>C p.L8P Substitution - Missense UD-SCC-2 COSM4162401 c.37T>C p.W13R Substitution - Missense 5 COSM4333395 c.716A>T p.K239M Substitution - Missense 7:73318832-73318832 - B109-Tumor COSM1755346 c.336T>G p.G112G Substitution - coding silent 7:73324452-73324452 - ORL-48 COSM4162404 c.23T>C p.L8P Substitution - Missense T2969 COSM4736135 c.1056G>A p.E352E Substitution - coding silent 7:73313329-73313329 - Pat_60_B COSM5873023 c.163G>A p.V55M Substitution - Missense 7:73324625-73324625 - CAL33 COSM4162404 c.23T>C p.L8P Substitution - Missense WSU-HN13 COSM4162400 c.37T>C p.W13R Substitution - Missense SCC-9 COSM4162400 c.37T>C p.W13R Substitution - Missense TCGA-EE-A3JD-06 COSM4393976 c.125C>T p.S42F Substitution - Missense 7:73324663-73324663 - CSCC-27-T COSM4502645 c.618C>T p.A206A Substitution - coding silent 7:73318930-73318930 - T3498 COSM4736138 c.241C>T p.P81S Substitution - Missense 7:73324547-73324547 - WSU-HN8 COSM4162404 c.23T>C p.L8P Substitution - Missense TCGA-AA-3710-01 COSM1451944 c.997G>A p.D333N Substitution - Missense 7:73313388-73313388 - SCC-15 COSM4162400 c.37T>C p.W13R Substitution - Missense CSCC-55-T COSM4498881 c.529C>T p.R177C Substitution - Missense 7:73319019-73319019 - CSCC-31-T COSM4560889 c.860G>T p.R287L Substitution - Missense 7:73316579-73316579 - WSU-HN8 COSM4162405 c.23T>C p.L8P Substitution - Missense CLL047 COSM1292537 c.297C>T p.F99F Substitution - coding silent 7:73324491-73324491 - 8068577 COSM3394873 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - UM-SCC-11B COSM4162401 c.37T>C p.W13R Substitution - Missense YUGOE COSM1698741 c.846G>A p.W282* Substitution - Nonsense 7:73316593-73316593 - 6115115 COSM3394873 c.1084C>T p.R362C Substitution - Missense 7:73313301-73313301 - MDA-MB-435 COSM1673206 c.1174G>A p.G392S Substitution - Missense 7:73313211-73313211 - TCGA-AA-3710-01 COSM1451945 c.997G>A p.D333N Substitution - Missense 7:73313388-73313388 - TCGA-FW-A3R5-06 COSM3923910 c.174G>A p.Q58Q Substitution - coding silent 7:73324614-73324614 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.647052;Hs.647053 7q11.23 612548 2452319|CGAP|BC112152|G/T|coding|Leu466Leu|1440|Candidate; 2452319|CGAP|BC112154|G/T|coding|Leu466Leu|1440|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer C A Missense p.G196V c.587G>T 7 72732960 LUAD C G Missense p.K390N c.1170G>C 7 72727211 OV C T IntronicSNV . c.750-89G>A 7 72730777 CM C T Missense p.A248T c.742G>A 7 72732693 CM C T Missense p.A303T c.907G>A 7 72727474 UCEC C T Missense p.E226K c.676G>A 7 72732871 COREAD C T Missense p.R161Q c.482G>A 7 72734159 GBM C T Missense p.R52H c.155G>A 7 72738631 STAD C T Missense p.V281M c.841G>A 7 72730597 SCLC C T Missense p.V90M c.268G>A 7 72738518 STAD C T Synonymous p.L143L c.429G>A 7 72734212 LUAD C T Synonymous p.V186V c.558G>A 7 72732989 CM G A IntronicSNV . c.874+1492C>T 7 72729072 CM G A Missense p.P258S c.772C>T 7 72730666 CM G A Missense p.S42F c.125C>T 7 72738661 CM G A Synonymous p.A430A c.1290C>T 7 72727091 CM G A Synonymous p.C111C c.333C>T 7 72738453 UCEC G A Synonymous p.F99F c.297C>T 7 72738489 CLL G A Synonymous p.G261G c.783C>T 7 72730655 STAD G A Synonymous p.G383G c.1149C>T 7 72727232 LUAD G A Synonymous p.G62G c.186C>T 7 72738600 SCLC G A Synonymous p.L285L c.855C>T 7 72730583 CM G T Missense p.R331S c.991C>A 7 72727390 ESCA G T Missense p.S141Y c.422C>A 7 72734219 LUSC G T Synonymous p.I140I c.420C>A 7 72734221 STAD T A Missense p.E226V c.677A>T 7 72732870 LUSC T A Missense p.K243M c.728A>T 7 72732707 RCCC T A Missense p.T280S c.838A>T 7 72730600 ESCA T C Missense p.T280A c.838A>G 7 72730600 HNSC T G Missense p.E424D c.1272A>C 7 72727109 LUSC