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 18 77917935 77917935 + Missense_Mutation SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr18:77917935C>T c.850G>A c.(850-852)Gtc>Atc p.V284I BRCA 18 77917708 77917708 + Silent SNP G G A TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr18:77917708G>A c.1077C>T c.(1075-1077)agC>agT p.S359S CESC 18 77917738 77917738 + Silent SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr18:77917738G>A c.1047C>T c.(1045-1047)ctC>ctT p.L349L CESC 18 77918347 77918347 + Silent SNP G G A TCGA-EK-A2RC-01A-11D-A18J-09 TCGA-EK-A2RC-10A-01D-A18J-09 g.chr18:77918347G>A c.438C>T c.(436-438)atC>atT p.I146I COAD 18 77917689 77917689 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr18:77917689C>T c.1096G>A c.(1096-1098)Ggc>Agc p.G366S COAD 18 77917845 77917845 + Frame_Shift_Del DEL G G - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr18:77917845delG c.940delC c.(940-942)cagfs p.Q314fs COAD 18 77917854 77917854 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr18:77917854G>A c.931C>T c.(931-933)Cgt>Tgt p.R311C COAD 18 77918073 77918073 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr18:77918073C>T c.712G>A c.(712-714)Gcc>Acc p.A238T COAD 18 77918086 77918086 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr18:77918086C>T c.699G>A c.(697-699)acG>acA p.T233T COAD 18 77918230 77918230 + Silent SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr18:77918230G>A c.555C>T c.(553-555)caC>caT p.H185H COAD 18 77918321 77918321 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr18:77918321G>A c.464C>T c.(463-465)aCg>aTg p.T155M COAD 18 77960761 77960761 + Missense_Mutation SNP C C G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr18:77960761C>G c.127G>C c.(127-129)Gaa>Caa p.E43Q COADREAD 18 77917689 77917689 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr18:77917689C>T c.1096G>A c.(1096-1098)Ggc>Agc p.G366S COADREAD 18 77917845 77917845 + Frame_Shift_Del DEL G G - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr18:77917845delG c.940delC c.(940-942)cagfs p.Q314fs COADREAD 18 77917854 77917854 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr18:77917854G>A c.931C>T c.(931-933)Cgt>Tgt p.R311C COADREAD 18 77918073 77918073 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr18:77918073C>T c.712G>A c.(712-714)Gcc>Acc p.A238T COADREAD 18 77918086 77918086 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr18:77918086C>T c.699G>A c.(697-699)acG>acA p.T233T COADREAD 18 77918230 77918230 + Silent SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr18:77918230G>A c.555C>T c.(553-555)caC>caT p.H185H COADREAD 18 77918321 77918321 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr18:77918321G>A c.464C>T c.(463-465)aCg>aTg p.T155M COADREAD 18 77960761 77960761 + Missense_Mutation SNP C C G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr18:77960761C>G c.127G>C c.(127-129)Gaa>Caa p.E43Q COADREAD 18 77960793 77960793 + Missense_Mutation SNP A A G TCGA-AG-3893-01A-01W-1073-09 TCGA-AG-3893-10A-01W-1073-09 g.chr18:77960793A>G c.95T>C c.(94-96)tTc>tCc p.F32S DLBC 18 77960661 77960661 + Missense_Mutation SNP T T C TCGA-FF-8061-01A-11D-2210-10 TCGA-FF-8061-10A-01D-2210-10 g.chr18:77960661T>C c.227A>G c.(226-228)aAt>aGt p.N76S ESCA 18 77917939 77917939 + Silent SNP C C T TCGA-R6-A6DN-01B-11D-A31U-09 TCGA-R6-A6DN-10A-01D-A31U-09 g.chr18:77917939C>T c.846G>A c.(844-846)ccG>ccA p.P282P GBM 18 77918374 77918374 + Silent SNP C C T TCGA-06-0877-01A-01W-0424-08 TCGA-06-0877-10A-01W-0424-08 g.chr18:77918374C>T c.411G>A c.(409-411)ccG>ccA p.P137P GBMLGG 18 77918260 77918260 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr18:77918260G>A c.525C>T c.(523-525)cgC>cgT p.R175R GBMLGG 18 77918374 77918374 + Silent SNP C C T TCGA-06-0877-01A-01W-0424-08 TCGA-06-0877-10A-01W-0424-08 g.chr18:77918374C>T c.411G>A c.(409-411)ccG>ccA p.P137P HNSC 18 77917833 77917833 + Missense_Mutation SNP C C T TCGA-CV-7101-01A-11D-2012-08 TCGA-CV-7101-11A-01D-2012-08 g.chr18:77917833C>T c.952G>A c.(952-954)Gcg>Acg p.A318T HNSC 18 77917940 77917940 + Missense_Mutation SNP G G A TCGA-QK-A6IG-01A-11D-A31L-08 TCGA-QK-A6IG-10A-01D-A31J-08 g.chr18:77917940G>A c.845C>T c.(844-846)cCg>cTg p.P282L HNSC 18 77917976 77917976 + Missense_Mutation SNP G G A TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr18:77917976G>A c.809C>T c.(808-810)tCg>tTg p.S270L HNSC 18 77918076 77918076 + Missense_Mutation SNP T T C TCGA-UF-A7J9-01A-12D-A34J-08 TCGA-UF-A7J9-10A-01D-A34M-08 g.chr18:77918076T>C c.709A>G c.(709-711)Atc>Gtc p.I237V HNSC 18 77918269 77918269 + Missense_Mutation SNP G G C TCGA-MZ-A7D7-01A-21D-A34J-08 TCGA-MZ-A7D7-10A-01D-A34M-08 g.chr18:77918269G>C c.516C>G c.(514-516)ttC>ttG p.F172L HNSC 18 77918383 77918383 + Silent SNP G G A TCGA-RS-A6TP-01A-12D-A34J-08 TCGA-RS-A6TP-10A-01D-A34M-08 g.chr18:77918383G>A c.402C>T c.(400-402)atC>atT p.I134I HNSC 18 77960666 77960666 + Silent SNP G G A TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr18:77960666G>A c.222C>T c.(220-222)atC>atT p.I74I HNSC 18 77960806 77960806 + Nonsense_Mutation SNP C C A TCGA-CV-6003-01A-11D-1683-08 TCGA-CV-6003-11A-01D-1683-08 g.chr18:77960806C>A c.82G>T c.(82-84)Gaa>Taa p.E28* LGG 18 77918260 77918260 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr18:77918260G>A c.525C>T c.(523-525)cgC>cgT p.R175R LUAD 18 77917844 77917845 + Frame_Shift_Ins INS - - G TCGA-17-Z020-01A-01W-0746-08 TCGA-17-Z020-11A-01W-0746-08 g.chr18:77917844_77917845insG c.940_941insC c.(940-942)cagfs p.Q314fs LUAD 18 78005177 78005177 + Missense_Mutation SNP C C G TCGA-55-8514-01A-11D-2393-08 TCGA-55-8514-10A-01D-2393-08 g.chr18:78005177C>G c.55G>C c.(55-57)Gtg>Ctg p.V19L LUSC 18 77960632 77960632 + Missense_Mutation SNP T T C TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr18:77960632T>C c.256A>G c.(256-258)Agt>Ggt p.S86G READ 18 77960793 77960793 + Missense_Mutation SNP A A G TCGA-AG-3893-01A-01W-1073-09 TCGA-AG-3893-10A-01W-1073-09 g.chr18:77960793A>G c.95T>C c.(94-96)tTc>tCc p.F32S SKCM 18 77917846 77917846 + Silent SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr18:77917846G>A c.939C>T c.(937-939)ccC>ccT p.P313P SKCM 18 77917847 77917847 + Missense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr18:77917847G>A c.938C>T c.(937-939)cCc>cTc p.P313L SKCM 18 77918229 77918229 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr18:77918229C>T c.556G>A c.(556-558)Ggg>Agg p.G186R SKCM 18 77918291 77918291 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr18:77918291C>T c.494G>A c.(493-495)gGc>gAc p.G165D SKCM 18 77918292 77918292 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr18:77918292C>T c.493G>A c.(493-495)Ggc>Agc p.G165S

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 18 77918108 77918108 single base substitution C T missense_variant G226E 677G>A BLCA-CN 18 77918156 77918156 single base substitution A G missense_variant L210P 629T>C BLCA-CN 18 78005253 78005253 single base substitution C T 5_prime_UTR_variant BLCA-CN 18 78005253 78005253 single base substitution C T upstream_gene_variant BLCA-US 18 77917935 77917935 single base substitution C T missense_variant V284I 850G>A BOCA-FR 18 78007073 78007073 single base substitution A T upstream_gene_variant BOCA-FR 18 78009144 78009144 single base substitution C T upstream_gene_variant BRCA-EU 18 77910756 77910756 single base substitution A C downstream_gene_variant BRCA-EU 18 77910951 77910951 single base substitution G C downstream_gene_variant BRCA-EU 18 77911545 77911545 single base substitution G C downstream_gene_variant BRCA-EU 18 77912259 77912259 single base substitution G A downstream_gene_variant BRCA-EU 18 77913613 77913613 single base substitution T C downstream_gene_variant BRCA-EU 18 77915720 77915720 single base substitution T A 3_prime_UTR_variant BRCA-EU 18 77917100 77917100 single base substitution T A 3_prime_UTR_variant BRCA-EU 18 77918589 77918589 single base substitution G A intron_variant BRCA-EU 18 77918677 77918677 single base substitution C G intron_variant BRCA-EU 18 77919240 77919240 single base substitution G T intron_variant BRCA-EU 18 77919339 77919339 single base substitution T C intron_variant BRCA-EU 18 77920952 77920952 single base substitution G C intron_variant BRCA-EU 18 77921040 77921040 single base substitution G A intron_variant BRCA-EU 18 77922121 77922121 single base substitution T G intron_variant BRCA-EU 18 77923083 77923083 single base substitution A G intron_variant BRCA-EU 18 77923549 77923549 single base substitution C G intron_variant BRCA-EU 18 77925191 77925235 multiple base substitution (>=2bp and <=200bp) CCGTGTGCAGGATAACACATGGGCAGTGTTGCGTGTGGATGTGTG CTGTGTGCCGGATAACACATGGGCAGTGTTGCGTGTGGACGTGT intron_variant BRCA-EU 18 77925261 77925261 single base substitution G A intron_variant BRCA-EU 18 77925891 77925891 single base substitution C T intron_variant BRCA-EU 18 77926974 77926974 single base substitution C T intron_variant BRCA-EU 18 77927254 77927254 single base substitution G T intron_variant BRCA-EU 18 77927407 77927407 single base substitution C T intron_variant BRCA-EU 18 77928693 77928693 single base substitution C A intron_variant BRCA-EU 18 77928842 77928842 single base substitution G C intron_variant BRCA-EU 18 77929508 77929508 single base substitution T C intron_variant BRCA-EU 18 77929648 77929648 single base substitution C T intron_variant BRCA-EU 18 77931590 77931590 single base substitution A T intron_variant BRCA-EU 18 77934014 77934014 single base substitution C T intron_variant BRCA-EU 18 77934711 77934711 single base substitution G C intron_variant BRCA-EU 18 77935330 77935330 single base substitution A G intron_variant BRCA-EU 18 77936130 77936130 single base substitution C T downstream_gene_variant BRCA-EU 18 77936130 77936130 single base substitution C T intron_variant BRCA-EU 18 77936473 77936473 single base substitution C A downstream_gene_variant BRCA-EU 18 77936473 77936473 single base substitution C A intron_variant BRCA-EU 18 77937463 77937463 single base substitution C A downstream_gene_variant BRCA-EU 18 77937463 77937463 single base substitution C A intron_variant BRCA-EU 18 77937743 77937743 single base substitution G C downstream_gene_variant BRCA-EU 18 77937743 77937743 single base substitution G C intron_variant BRCA-EU 18 77938176 77938176 single base substitution G A downstream_gene_variant BRCA-EU 18 77938176 77938176 single base substitution G A intron_variant BRCA-EU 18 77940448 77940448 single base substitution A C downstream_gene_variant BRCA-EU 18 77940448 77940448 single base substitution A C intron_variant BRCA-EU 18 77942651 77942651 single base substitution A T intron_variant BRCA-EU 18 77943053 77943053 single base substitution G A intron_variant BRCA-EU 18 77944461 77944461 insertion of <=200bp - C intron_variant BRCA-EU 18 77944886 77944886 single base substitution G C intron_variant BRCA-EU 18 77948511 77948511 single base substitution C A intron_variant BRCA-EU 18 77948707 77948707 single base substitution A C intron_variant BRCA-EU 18 77951719 77951719 single base substitution G A intron_variant BRCA-EU 18 77951726 77951726 single base substitution C G intron_variant BRCA-EU 18 77953295 77953295 single base substitution C T intron_variant BRCA-EU 18 77956134 77956134 single base substitution G C intron_variant BRCA-EU 18 77956150 77956150 single base substitution T G intron_variant BRCA-EU 18 77956250 77956250 single base substitution A T intron_variant BRCA-EU 18 77956334 77956334 single base substitution A G intron_variant BRCA-EU 18 77957149 77957149 single base substitution C A intron_variant BRCA-EU 18 77957498 77957498 single base substitution G T intron_variant BRCA-EU 18 77959029 77959029 single base substitution G C intron_variant BRCA-EU 18 77960940 77960940 single base substitution C G intron_variant BRCA-EU 18 77960940 77960940 single base substitution C G upstream_gene_variant BRCA-EU 18 77960943 77960943 single base substitution C A intron_variant BRCA-EU 18 77960943 77960943 single base substitution C A upstream_gene_variant BRCA-EU 18 77961882 77961882 single base substitution C T intron_variant BRCA-EU 18 77961882 77961882 single base substitution C T upstream_gene_variant BRCA-EU 18 77962686 77962686 single base substitution G A intron_variant BRCA-EU 18 77962686 77962686 single base substitution G A upstream_gene_variant BRCA-EU 18 77966307 77966307 single base substitution A T intron_variant BRCA-EU 18 77966341 77966341 single base substitution G C intron_variant BRCA-EU 18 77968306 77968306 single base substitution C T intron_variant BRCA-EU 18 77968827 77968827 single base substitution G A intron_variant BRCA-EU 18 77969936 77969936 deletion of <=200bp A - intron_variant BRCA-EU 18 77970166 77970166 single base substitution C T intron_variant BRCA-EU 18 77972696 77972696 single base substitution T C intron_variant BRCA-EU 18 77973497 77973497 single base substitution G T intron_variant BRCA-EU 18 77975680 77975680 single base substitution T C intron_variant BRCA-EU 18 77976098 77976098 single base substitution C T intron_variant BRCA-EU 18 77976187 77976187 single base substitution C A intron_variant BRCA-EU 18 77976710 77976710 single base substitution C T intron_variant BRCA-EU 18 77977246 77977246 single base substitution C A intron_variant BRCA-EU 18 77978105 77978105 single base substitution C G intron_variant BRCA-EU 18 77979760 77979760 single base substitution T A intron_variant BRCA-EU 18 77982659 77982659 single base substitution G A intron_variant BRCA-EU 18 77983048 77983048 single base substitution A G intron_variant BRCA-EU 18 77986292 77986292 single base substitution C G intron_variant BRCA-EU 18 77986576 77986576 single base substitution C G intron_variant BRCA-EU 18 77987699 77987699 single base substitution C T intron_variant BRCA-EU 18 77989361 77989361 single base substitution G A intron_variant BRCA-EU 18 77990607 77990607 single base substitution C G intron_variant BRCA-EU 18 77992069 77992069 single base substitution C T intron_variant BRCA-EU 18 77992876 77992876 single base substitution C G intron_variant BRCA-EU 18 77996383 77996383 single base substitution A C intron_variant BRCA-EU 18 77998701 77998701 single base substitution C A intron_variant BRCA-EU 18 77999805 77999805 single base substitution G T intron_variant BRCA-EU 18 78000505 78000505 single base substitution G A intron_variant BRCA-EU 18 78001349 78001349 single base substitution A G intron_variant BRCA-EU 18 78003698 78003698 single base substitution G T intron_variant BRCA-EU 18 78004946 78004946 single base substitution C T intron_variant BRCA-EU 18 78008538 78008538 single base substitution C T upstream_gene_variant BRCA-EU 18 78009047 78009047 single base substitution T C upstream_gene_variant BRCA-EU 18 78009499 78009499 single base substitution T A upstream_gene_variant BRCA-EU 18 78009990 78009990 single base substitution G A upstream_gene_variant BRCA-FR 18 77910756 77910756 single base substitution A C downstream_gene_variant BRCA-FR 18 77911545 77911545 single base substitution G C downstream_gene_variant BRCA-FR 18 77915720 77915720 single base substitution T A 3_prime_UTR_variant BRCA-FR 18 77918677 77918677 single base substitution C G intron_variant BRCA-FR 18 77920952 77920952 single base substitution G C intron_variant BRCA-FR 18 77921040 77921040 single base substitution G A intron_variant BRCA-FR 18 77927407 77927407 single base substitution C T intron_variant BRCA-FR 18 77928693 77928693 single base substitution C A intron_variant BRCA-FR 18 77934262 77934262 single base substitution C A intron_variant BRCA-FR 18 77934711 77934711 single base substitution G C intron_variant BRCA-FR 18 77953295 77953295 single base substitution C T intron_variant BRCA-FR 18 77956134 77956134 single base substitution G C intron_variant BRCA-FR 18 77959029 77959029 single base substitution G C intron_variant BRCA-FR 18 77967010 77967010 single base substitution A C intron_variant BRCA-FR 18 77976710 77976710 single base substitution C T intron_variant BRCA-FR 18 77984156 77984156 single base substitution C T intron_variant BRCA-FR 18 77989361 77989361 single base substitution G A intron_variant BRCA-FR 18 77991543 77991543 single base substitution G A intron_variant BRCA-FR 18 77999482 77999482 single base substitution T G intron_variant BRCA-FR 18 77999805 77999805 single base substitution G T intron_variant BRCA-FR 18 78003698 78003698 single base substitution G T intron_variant BRCA-FR 18 78009990 78009990 single base substitution G A upstream_gene_variant BRCA-UK 18 77925261 77925261 single base substitution G A intron_variant BRCA-UK 18 77954082 77954089 deletion of <=200bp AAAAATAT - intron_variant BRCA-UK 18 77957149 77957149 single base substitution C A intron_variant BRCA-UK 18 77965175 77965175 single base substitution C A intron_variant BRCA-UK 18 77965175 77965175 single base substitution C A upstream_gene_variant BRCA-UK 18 78000505 78000505 single base substitution G A intron_variant BRCA-US 18 77917708 77917708 single base substitution G A synonymous_variant S359S 1077C>T BTCA-JP 18 77917884 77917884 single base substitution C T missense_variant V301I 901G>A BTCA-JP 18 77918241 77918241 single base substitution C T missense_variant V182M 544G>A BTCA-JP 18 77921468 77921468 single base substitution G A intron_variant BTCA-JP 18 77960675 77960675 single base substitution C G synonymous_variant L30L 90G>C BTCA-JP 18 77960675 77960675 single base substitution C G synonymous_variant L71L 213G>C BTCA-JP 18 77960836 77960836 single base substitution T G intron_variant BTCA-JP 18 77960836 77960836 single base substitution T G upstream_gene_variant CESC-US 18 77917738 77917738 single base substitution G A synonymous_variant L349L 1047C>T CESC-US 18 77918347 77918347 single base substitution G A synonymous_variant I146I 438C>T CESC-US 18 77920423 77920423 single base substitution G T intron_variant CLLE-ES 18 77919564 77919564 single base substitution G C intron_variant CLLE-ES 18 77930118 77930118 single base substitution C T intron_variant CLLE-ES 18 77946124 77946124 single base substitution C T intron_variant CLLE-ES 18 77953125 77953125 single base substitution A T intron_variant CLLE-ES 18 77966855 77966855 single base substitution C T intron_variant CLLE-ES 18 77970539 77970539 single base substitution C T intron_variant CLLE-ES 18 77978280 77978280 single base substitution G T intron_variant CLLE-ES 18 77984113 77984113 single base substitution G A intron_variant CLLE-ES 18 77994671 77994671 single base substitution C T intron_variant CLLE-ES 18 77999727 77999727 single base substitution G C intron_variant CLLE-ES 18 78007507 78007507 single base substitution T C upstream_gene_variant COAD-US 18 77917845 77917845 deletion of <=200bp G - frameshift_variant Q314 COAD-US 18 77918073 77918073 single base substitution C T missense_variant A238T 712G>A COAD-US 18 77918080 77918080 single base substitution C A missense_variant M235I 705G>T COAD-US 18 77918321 77918321 single base substitution G A missense_variant T155M 464C>T COAD-US 18 77960761 77960761 single base substitution C G missense_variant E2Q 4G>C COAD-US 18 77960761 77960761 single base substitution C G missense_variant E43Q 127G>C COCA-CN 18 77917790 77917790 single base substitution G A missense_variant A332V 995C>T COCA-CN 18 77917875 77917875 single base substitution C T missense_variant E304K 910G>A COCA-CN 18 77918197 77918197 single base substitution C T synonymous_variant S196S 588G>A COCA-CN 18 77918278 77918278 single base substitution C T synonymous_variant P169P 507G>A COCA-CN 18 77955210 77955210 single base substitution C T intron_variant COCA-CN 18 77992692 77992692 single base substitution T C intron_variant COCA-CN 18 77992757 77992757 single base substitution T A intron_variant COCA-CN 18 77993056 77993056 single base substitution G A intron_variant COCA-CN 18 77993069 77993069 single base substitution A G intron_variant COCA-CN 18 77993106 77993106 single base substitution T G intron_variant COCA-CN 18 78005169 78005169 single base substitution G T synonymous_variant V21V 63C>A EOPC-DE 18 77920079 77920079 single base substitution G A intron_variant EOPC-DE 18 77943799 77943799 single base substitution A G intron_variant EOPC-DE 18 77957999 77957999 single base substitution A T intron_variant EOPC-DE 18 77978474 77978474 single base substitution T A intron_variant EOPC-DE 18 77982203 77982203 single base substitution G T intron_variant ESAD-UK 18 77913753 77913753 single base substitution A G downstream_gene_variant ESAD-UK 18 77914347 77914347 deletion of <=200bp T - downstream_gene_variant ESAD-UK 18 77919987 77919987 single base substitution G T intron_variant ESAD-UK 18 77923184 77923184 single base substitution A G intron_variant ESAD-UK 18 77923938 77923938 single base substitution G A intron_variant ESAD-UK 18 77925102 77925102 single base substitution G A intron_variant ESAD-UK 18 77928826 77928826 single base substitution C A intron_variant ESAD-UK 18 77930224 77930224 single base substitution G C intron_variant ESAD-UK 18 77930794 77930794 single base substitution C T intron_variant ESAD-UK 18 77931486 77931486 single base substitution T C intron_variant ESAD-UK 18 77931522 77931522 single base substitution C A intron_variant ESAD-UK 18 77932194 77932194 single base substitution T C intron_variant ESAD-UK 18 77932949 77932949 single base substitution G A intron_variant ESAD-UK 18 77933171 77933171 single base substitution G T intron_variant ESAD-UK 18 77936412 77936412 single base substitution A G downstream_gene_variant ESAD-UK 18 77936412 77936412 single base substitution A G intron_variant ESAD-UK 18 77940163 77940163 single base substitution A T downstream_gene_variant ESAD-UK 18 77940163 77940163 single base substitution A T intron_variant ESAD-UK 18 77940711 77940711 single base substitution G T downstream_gene_variant ESAD-UK 18 77940711 77940711 single base substitution G T intron_variant ESAD-UK 18 77942154 77942154 single base substitution C T intron_variant ESAD-UK 18 77943212 77943212 single base substitution G A intron_variant ESAD-UK 18 77943730 77943730 single base substitution C T intron_variant ESAD-UK 18 77944839 77944839 single base substitution G A intron_variant ESAD-UK 18 77945391 77945391 single base substitution G T intron_variant ESAD-UK 18 77945727 77945727 single base substitution C T intron_variant ESAD-UK 18 77949181 77949181 single base substitution C T intron_variant ESAD-UK 18 77950705 77950705 single base substitution G A intron_variant ESAD-UK 18 77952225 77952225 single base substitution T G intron_variant ESAD-UK 18 77952545 77952545 single base substitution A C intron_variant ESAD-UK 18 77956797 77956797 single base substitution T A intron_variant ESAD-UK 18 77957231 77957231 single base substitution C T intron_variant ESAD-UK 18 77958174 77958174 single base substitution G A intron_variant ESAD-UK 18 77959594 77959594 single base substitution C T intron_variant ESAD-UK 18 77959917 77959917 single base substitution G A intron_variant ESAD-UK 18 77963840 77963840 single base substitution G A intron_variant ESAD-UK 18 77963840 77963840 single base substitution G A upstream_gene_variant ESAD-UK 18 77965519 77965519 single base substitution C T intron_variant ESAD-UK 18 77965519 77965519 single base substitution C T upstream_gene_variant ESAD-UK 18 77966199 77966199 single base substitution C T intron_variant ESAD-UK 18 77967892 77967892 single base substitution C T intron_variant ESAD-UK 18 77968430 77968430 single base substitution C G intron_variant ESAD-UK 18 77970718 77970718 single base substitution A G intron_variant ESAD-UK 18 77971489 77971489 deletion of <=200bp A - intron_variant ESAD-UK 18 77972813 77972813 insertion of <=200bp - A intron_variant ESAD-UK 18 77974291 77974291 single base substitution T A intron_variant ESAD-UK 18 77974573 77974573 single base substitution A T intron_variant ESAD-UK 18 77978620 77978620 single base substitution A C intron_variant ESAD-UK 18 77979961 77979961 single base substitution A T intron_variant ESAD-UK 18 77980773 77980773 single base substitution G A intron_variant ESAD-UK 18 77982443 77982443 single base substitution G A intron_variant ESAD-UK 18 77983733 77983733 single base substitution G T intron_variant ESAD-UK 18 77983992 77983992 insertion of <=200bp - CCAGCTAC intron_variant ESAD-UK 18 77988535 77988535 single base substitution C A intron_variant ESAD-UK 18 77988542 77988542 single base substitution C T intron_variant ESAD-UK 18 77990288 77990288 single base substitution A C intron_variant ESAD-UK 18 77990590 77990590 single base substitution C A intron_variant ESAD-UK 18 77992207 77992207 single base substitution A C intron_variant ESAD-UK 18 77996215 77996215 single base substitution G A intron_variant ESAD-UK 18 77997638 77997638 single base substitution C T intron_variant ESAD-UK 18 77999830 77999830 single base substitution G T intron_variant ESAD-UK 18 78000947 78000947 single base substitution T C intron_variant ESAD-UK 18 78001640 78001640 single base substitution G T intron_variant ESAD-UK 18 78004850 78004850 single base substitution G A intron_variant ESAD-UK 18 78005970 78005970 single base substitution G A upstream_gene_variant ESAD-UK 18 78008337 78008337 single base substitution C G upstream_gene_variant ESAD-UK 18 78008850 78008850 single base substitution T A upstream_gene_variant ESAD-UK 18 78009201 78009201 single base substitution C T upstream_gene_variant ESAD-UK 18 78009984 78009984 single base substitution G A upstream_gene_variant ESAD-UK 18 78010125 78010125 single base substitution G A upstream_gene_variant ESAD-UK 18 78010338 78010338 single base substitution T G upstream_gene_variant ESCA-CN 18 77927112 77927112 single base substitution G A intron_variant ESCA-CN 18 77935855 77935855 insertion of <=200bp - AC downstream_gene_variant ESCA-CN 18 77935855 77935855 insertion of <=200bp - AC intron_variant ESCA-CN 18 77960723 77960723 single base substitution G C missense_variant I14M 42C>G ESCA-CN 18 77960723 77960723 single base substitution G C missense_variant I55M 165C>G GBM-US 18 77918374 77918374 single base substitution C T synonymous_variant P137P 411G>A LAML-KR 18 77935297 77935297 single base substitution C T intron_variant LAML-KR 18 77935458 77935458 single base substitution A G intron_variant LAML-KR 18 77935570 77935570 single base substitution G C intron_variant LAML-KR 18 77935591 77935591 single base substitution T C intron_variant LAML-KR 18 77943864 77943864 single base substitution C T intron_variant LAML-KR 18 77943873 77943873 single base substitution C A intron_variant LAML-KR 18 77943975 77943975 single base substitution A T intron_variant LAML-KR 18 77944017 77944017 single base substitution G A intron_variant LAML-KR 18 77944020 77944020 single base substitution T C intron_variant LAML-KR 18 77944386 77944386 single base substitution C T intron_variant LICA-CN 18 77960658 77960658 single base substitution T C missense_variant D36G 107A>G LICA-CN 18 77960658 77960658 single base substitution T C missense_variant D77G 230A>G LICA-FR 18 77912790 77912790 single base substitution A C downstream_gene_variant LICA-FR 18 77913108 77913108 single base substitution A G downstream_gene_variant LICA-FR 18 77913964 77913964 single base substitution G C downstream_gene_variant LICA-FR 18 77917713 77917713 single base substitution G A missense_variant H358Y 1072C>T LICA-FR 18 77917906 77917906 single base substitution C A synonymous_variant A293A 879G>T LICA-FR 18 77918006 77918010 deletion of <=200bp CCGCC - frameshift_variant GG259 LICA-FR 18 77944045 77944045 single base substitution T A intron_variant LICA-FR 18 77992757 77992757 single base substitution T A intron_variant LICA-FR 18 77992979 77992979 single base substitution A G intron_variant LINC-JP 18 77915439 77915439 single base substitution G C 3_prime_UTR_variant LINC-JP 18 77921477 77921477 single base substitution G A intron_variant LINC-JP 18 77925151 77925151 single base substitution C T intron_variant LINC-JP 18 77926508 77926508 single base substitution T C intron_variant LINC-JP 18 77936864 77936864 single base substitution A G downstream_gene_variant LINC-JP 18 77936864 77936864 single base substitution A G intron_variant LINC-JP 18 77936922 77936922 single base substitution T G downstream_gene_variant LINC-JP 18 77936922 77936922 single base substitution T G intron_variant LINC-JP 18 77936960 77936960 single base substitution A C downstream_gene_variant LINC-JP 18 77936960 77936960 single base substitution A C intron_variant LINC-JP 18 77937107 77937107 deletion of <=200bp T - downstream_gene_variant LINC-JP 18 77937107 77937107 deletion of <=200bp T - intron_variant LIRI-JP 18 77911982 77911982 single base substitution A G downstream_gene_variant LIRI-JP 18 77913923 77913923 single base substitution C G downstream_gene_variant LIRI-JP 18 77924193 77924193 single base substitution G T intron_variant LIRI-JP 18 77931823 77931823 single base substitution G A intron_variant LIRI-JP 18 77939256 77939256 single base substitution C T downstream_gene_variant LIRI-JP 18 77939256 77939256 single base substitution C T intron_variant LIRI-JP 18 77940870 77940870 single base substitution G A 3_prime_UTR_variant LIRI-JP 18 77940870 77940870 single base substitution G A intron_variant LIRI-JP 18 77951717 77951717 single base substitution C T intron_variant LIRI-JP 18 77952195 77952195 single base substitution C T intron_variant LIRI-JP 18 77952975 77952980 deletion of <=200bp AGCCCC - intron_variant LIRI-JP 18 77954528 77954528 single base substitution A G intron_variant LIRI-JP 18 77955259 77955259 single base substitution C T intron_variant LIRI-JP 18 77960175 77960175 single base substitution T C intron_variant LIRI-JP 18 77960338 77960338 single base substitution T C intron_variant LIRI-JP 18 77960831 77960831 single base substitution C T intron_variant LIRI-JP 18 77960831 77960831 single base substitution C T upstream_gene_variant LIRI-JP 18 77963893 77963893 single base substitution G A intron_variant LIRI-JP 18 77963893 77963893 single base substitution G A upstream_gene_variant LIRI-JP 18 77978766 77978766 single base substitution T C intron_variant LIRI-JP 18 77981798 77981798 single base substitution C T intron_variant LIRI-JP 18 77984639 77984639 single base substitution C T intron_variant LIRI-JP 18 77985226 77985226 single base substitution A T intron_variant LIRI-JP 18 77987862 77987862 single base substitution T C intron_variant LIRI-JP 18 77991395 77991395 single base substitution C T intron_variant LIRI-JP 18 78000089 78000089 deletion of <=200bp C - intron_variant LIRI-JP 18 78006248 78006248 single base substitution C T upstream_gene_variant LIRI-JP 18 78007570 78007570 single base substitution T C upstream_gene_variant LIRI-JP 18 78010324 78010324 single base substitution T G upstream_gene_variant LUSC-KR 18 77915698 77915698 single base substitution A C 3_prime_UTR_variant LUSC-KR 18 77917264 77917264 single base substitution T C 3_prime_UTR_variant LUSC-KR 18 77917698 77917698 single base substitution G A missense_variant P363S 1087C>T LUSC-KR 18 77922264 77922264 single base substitution G C intron_variant LUSC-KR 18 77925243 77925243 single base substitution T A intron_variant LUSC-KR 18 77925283 77925283 single base substitution T C intron_variant LUSC-KR 18 77927028 77927028 single base substitution A G intron_variant LUSC-KR 18 77927112 77927112 single base substitution G A intron_variant LUSC-KR 18 77927314 77927314 single base substitution G T intron_variant LUSC-KR 18 77927608 77927608 single base substitution T C intron_variant LUSC-KR 18 77927866 77927866 single base substitution A G intron_variant LUSC-KR 18 77931456 77931456 single base substitution C G intron_variant LUSC-KR 18 77933877 77933877 single base substitution T A intron_variant LUSC-KR 18 77934807 77934807 single base substitution C G intron_variant LUSC-KR 18 77943878 77943878 single base substitution G C intron_variant LUSC-KR 18 77944017 77944017 single base substitution G A intron_variant LUSC-KR 18 77948797 77948797 single base substitution T A intron_variant LUSC-KR 18 77953707 77953707 single base substitution G C intron_variant LUSC-KR 18 77959763 77959763 single base substitution T A intron_variant LUSC-KR 18 77962320 77962320 single base substitution C G intron_variant LUSC-KR 18 77962320 77962320 single base substitution C G upstream_gene_variant LUSC-KR 18 77964995 77964995 single base substitution T C intron_variant LUSC-KR 18 77964995 77964995 single base substitution T C upstream_gene_variant LUSC-KR 18 77966424 77966424 single base substitution C A intron_variant LUSC-KR 18 77966457 77966457 single base substitution C T intron_variant LUSC-KR 18 77968636 77968636 single base substitution C A intron_variant LUSC-KR 18 77969232 77969232 single base substitution T A intron_variant LUSC-KR 18 77974868 77974868 single base substitution C A intron_variant LUSC-KR 18 77975731 77975731 single base substitution C T intron_variant LUSC-KR 18 77978475 77978475 single base substitution C T intron_variant LUSC-KR 18 77985335 77985335 single base substitution C A intron_variant LUSC-KR 18 77986750 77986750 single base substitution T C intron_variant LUSC-KR 18 77987763 77987763 single base substitution C A intron_variant LUSC-KR 18 78006004 78006004 single base substitution G T upstream_gene_variant LUSC-US 18 77960632 77960632 single base substitution T C missense_variant S45G 133A>G LUSC-US 18 77960632 77960632 single base substitution T C missense_variant S86G 256A>G MALY-DE 18 77913114 77913114 deletion of <=200bp T - downstream_gene_variant MALY-DE 18 77925548 77925548 single base substitution A C intron_variant MALY-DE 18 77927763 77927763 single base substitution A T intron_variant MALY-DE 18 77938753 77938753 single base substitution G C downstream_gene_variant MALY-DE 18 77938753 77938753 single base substitution G C intron_variant MALY-DE 18 77944355 77944355 single base substitution G A intron_variant MALY-DE 18 77947262 77947262 single base substitution G A intron_variant MALY-DE 18 77948029 77948029 single base substitution T C intron_variant MALY-DE 18 77950727 77950727 single base substitution G C intron_variant MALY-DE 18 77952474 77952474 single base substitution C T intron_variant MALY-DE 18 77967543 77967543 single base substitution A G intron_variant MALY-DE 18 77979810 77979810 single base substitution T G intron_variant MALY-DE 18 77983041 77983041 single base substitution C T intron_variant MALY-DE 18 77989712 77989712 single base substitution C T intron_variant MELA-AU 18 77910984 77910984 single base substitution G A downstream_gene_variant MELA-AU 18 77911293 77911293 single base substitution C T downstream_gene_variant MELA-AU 18 77912608 77912608 single base substitution G A downstream_gene_variant MELA-AU 18 77914099 77914099 single base substitution G A downstream_gene_variant MELA-AU 18 77914485 77914485 single base substitution C T downstream_gene_variant MELA-AU 18 77914524 77914524 single base substitution A G downstream_gene_variant MELA-AU 18 77915189 77915189 single base substitution G T 3_prime_UTR_variant MELA-AU 18 77915569 77915569 single base substitution G A 3_prime_UTR_variant MELA-AU 18 77918298 77918299 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant HR162HW MELA-AU 18 77918887 77918887 single base substitution G T intron_variant MELA-AU 18 77920553 77920553 single base substitution T C intron_variant MELA-AU 18 77922306 77922307 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 18 77922446 77922446 single base substitution C T intron_variant MELA-AU 18 77922512 77922512 single base substitution G A intron_variant MELA-AU 18 77923060 77923060 single base substitution A G intron_variant MELA-AU 18 77923122 77923122 single base substitution G A intron_variant MELA-AU 18 77923875 77923875 single base substitution G A intron_variant MELA-AU 18 77924156 77924156 single base substitution C T intron_variant MELA-AU 18 77924256 77924256 single base substitution G A intron_variant MELA-AU 18 77924859 77924859 single base substitution C T intron_variant MELA-AU 18 77924919 77924919 single base substitution G A intron_variant MELA-AU 18 77925601 77925601 single base substitution G A intron_variant MELA-AU 18 77925900 77925900 single base substitution G A intron_variant MELA-AU 18 77925952 77925952 single base substitution G A intron_variant MELA-AU 18 77926921 77926921 single base substitution G A intron_variant MELA-AU 18 77927222 77927222 single base substitution G A intron_variant MELA-AU 18 77927314 77927314 single base substitution G A intron_variant MELA-AU 18 77927409 77927409 single base substitution G A intron_variant MELA-AU 18 77927877 77927877 single base substitution G A intron_variant MELA-AU 18 77927935 77927935 single base substitution C T intron_variant MELA-AU 18 77928190 77928190 single base substitution G A intron_variant MELA-AU 18 77929174 77929174 single base substitution G A intron_variant MELA-AU 18 77929190 77929190 single base substitution G A intron_variant MELA-AU 18 77929731 77929731 single base substitution A G intron_variant MELA-AU 18 77931595 77931595 single base substitution C A intron_variant MELA-AU 18 77931770 77931770 single base substitution C A intron_variant MELA-AU 18 77932261 77932261 single base substitution G A intron_variant MELA-AU 18 77932339 77932339 single base substitution C T intron_variant MELA-AU 18 77933919 77933919 single base substitution C T intron_variant MELA-AU 18 77934956 77934957 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 18 77934997 77934997 single base substitution C A intron_variant MELA-AU 18 77935206 77935206 single base substitution G A intron_variant MELA-AU 18 77935264 77935264 single base substitution G A intron_variant MELA-AU 18 77935456 77935456 single base substitution G A intron_variant MELA-AU 18 77935629 77935629 single base substitution A G intron_variant MELA-AU 18 77935894 77935894 single base substitution G A downstream_gene_variant MELA-AU 18 77935894 77935894 single base substitution G A intron_variant MELA-AU 18 77935960 77935960 single base substitution T C downstream_gene_variant MELA-AU 18 77935960 77935960 single base substitution T C intron_variant MELA-AU 18 77936321 77936321 single base substitution G A downstream_gene_variant MELA-AU 18 77936321 77936321 single base substitution G A intron_variant MELA-AU 18 77936378 77936378 single base substitution C T downstream_gene_variant MELA-AU 18 77936378 77936378 single base substitution C T intron_variant MELA-AU 18 77937215 77937215 single base substitution G A downstream_gene_variant MELA-AU 18 77937215 77937215 single base substitution G A intron_variant MELA-AU 18 77937743 77937743 single base substitution G A downstream_gene_variant MELA-AU 18 77937743 77937743 single base substitution G A intron_variant MELA-AU 18 77938142 77938142 single base substitution C T downstream_gene_variant MELA-AU 18 77938142 77938142 single base substitution C T intron_variant MELA-AU 18 77938328 77938328 single base substitution G A downstream_gene_variant MELA-AU 18 77938328 77938328 single base substitution G A intron_variant MELA-AU 18 77938613 77938613 single base substitution G A downstream_gene_variant MELA-AU 18 77938613 77938613 single base substitution G A intron_variant MELA-AU 18 77938753 77938753 single base substitution G A downstream_gene_variant MELA-AU 18 77938753 77938753 single base substitution G A intron_variant MELA-AU 18 77938799 77938799 single base substitution G A downstream_gene_variant MELA-AU 18 77938799 77938799 single base substitution G A intron_variant MELA-AU 18 77938876 77938877 multiple base substitution (>=2bp and <=200bp) CC GT downstream_gene_variant MELA-AU 18 77938876 77938877 multiple base substitution (>=2bp and <=200bp) CC GT intron_variant MELA-AU 18 77939135 77939136 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 18 77939135 77939136 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 18 77939320 77939320 single base substitution G A downstream_gene_variant MELA-AU 18 77939320 77939320 single base substitution G A intron_variant MELA-AU 18 77939360 77939360 single base substitution C T downstream_gene_variant MELA-AU 18 77939360 77939360 single base substitution C T intron_variant MELA-AU 18 77939398 77939398 single base substitution G A downstream_gene_variant MELA-AU 18 77939398 77939398 single base substitution G A intron_variant MELA-AU 18 77939469 77939469 single base substitution G A downstream_gene_variant MELA-AU 18 77939469 77939469 single base substitution G A intron_variant MELA-AU 18 77939638 77939638 single base substitution G A downstream_gene_variant MELA-AU 18 77939638 77939638 single base substitution G A intron_variant MELA-AU 18 77939673 77939673 single base substitution C T downstream_gene_variant MELA-AU 18 77939673 77939673 single base substitution C T intron_variant MELA-AU 18 77942404 77942404 single base substitution G A intron_variant MELA-AU 18 77942909 77942909 single base substitution A G intron_variant MELA-AU 18 77943470 77943470 single base substitution G A intron_variant MELA-AU 18 77944537 77944537 single base substitution G A intron_variant MELA-AU 18 77945486 77945486 single base substitution G C intron_variant MELA-AU 18 77945582 77945583 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 18 77946222 77946222 single base substitution G A intron_variant MELA-AU 18 77946225 77946225 single base substitution A T intron_variant MELA-AU 18 77946399 77946399 single base substitution G A intron_variant MELA-AU 18 77946542 77946542 single base substitution G A intron_variant MELA-AU 18 77946658 77946658 single base substitution C T intron_variant MELA-AU 18 77947446 77947446 single base substitution G A intron_variant MELA-AU 18 77948443 77948443 single base substitution G A intron_variant MELA-AU 18 77948518 77948518 single base substitution G A intron_variant MELA-AU 18 77949288 77949288 single base substitution C T intron_variant MELA-AU 18 77949617 77949617 single base substitution G A intron_variant MELA-AU 18 77950380 77950381 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 18 77950820 77950820 single base substitution C T intron_variant MELA-AU 18 77951116 77951116 single base substitution G A intron_variant MELA-AU 18 77951133 77951134 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 18 77951250 77951250 single base substitution C T intron_variant MELA-AU 18 77951787 77951787 single base substitution G A intron_variant MELA-AU 18 77951988 77951988 single base substitution G A intron_variant MELA-AU 18 77952524 77952524 single base substitution T C intron_variant MELA-AU 18 77952578 77952578 single base substitution G A intron_variant MELA-AU 18 77952930 77952930 single base substitution G A intron_variant MELA-AU 18 77953326 77953326 single base substitution C T intron_variant MELA-AU 18 77953768 77953768 single base substitution A G intron_variant MELA-AU 18 77955415 77955415 single base substitution G A intron_variant MELA-AU 18 77955416 77955416 single base substitution G A intron_variant MELA-AU 18 77955863 77955863 single base substitution A C intron_variant MELA-AU 18 77957305 77957305 single base substitution C T intron_variant MELA-AU 18 77957708 77957708 single base substitution A C intron_variant MELA-AU 18 77957717 77957717 single base substitution A G intron_variant MELA-AU 18 77960829 77960829 single base substitution G A intron_variant MELA-AU 18 77960829 77960829 single base substitution G A upstream_gene_variant MELA-AU 18 77961188 77961188 single base substitution G A intron_variant MELA-AU 18 77961188 77961188 single base substitution G A upstream_gene_variant MELA-AU 18 77961337 77961337 single base substitution G A intron_variant MELA-AU 18 77961337 77961337 single base substitution G A upstream_gene_variant MELA-AU 18 77961779 77961779 single base substitution G A intron_variant MELA-AU 18 77961779 77961779 single base substitution G A upstream_gene_variant MELA-AU 18 77962787 77962787 single base substitution A T intron_variant MELA-AU 18 77962787 77962787 single base substitution A T upstream_gene_variant MELA-AU 18 77962994 77962994 single base substitution G A intron_variant MELA-AU 18 77962994 77962994 single base substitution G A upstream_gene_variant MELA-AU 18 77963104 77963104 single base substitution G A intron_variant MELA-AU 18 77963104 77963104 single base substitution G A upstream_gene_variant MELA-AU 18 77963830 77963830 single base substitution C A intron_variant MELA-AU 18 77963830 77963830 single base substitution C A upstream_gene_variant MELA-AU 18 77964323 77964323 single base substitution C T intron_variant MELA-AU 18 77964323 77964323 single base substitution C T upstream_gene_variant MELA-AU 18 77964823 77964823 single base substitution T G intron_variant MELA-AU 18 77964823 77964823 single base substitution T G upstream_gene_variant MELA-AU 18 77966545 77966545 deletion of <=200bp G - intron_variant MELA-AU 18 77966770 77966770 single base substitution G A intron_variant MELA-AU 18 77967330 77967330 single base substitution G A intron_variant MELA-AU 18 77969126 77969126 single base substitution A G intron_variant MELA-AU 18 77969478 77969478 single base substitution G A intron_variant MELA-AU 18 77969898 77969898 single base substitution T A intron_variant MELA-AU 18 77970159 77970159 single base substitution C T intron_variant MELA-AU 18 77970528 77970528 single base substitution G A intron_variant MELA-AU 18 77970586 77970586 single base substitution G A intron_variant MELA-AU 18 77971681 77971681 single base substitution A T intron_variant MELA-AU 18 77972274 77972274 single base substitution G A intron_variant MELA-AU 18 77972639 77972639 single base substitution G A intron_variant MELA-AU 18 77974063 77974063 single base substitution G A intron_variant MELA-AU 18 77974064 77974064 single base substitution G A intron_variant MELA-AU 18 77974092 77974092 single base substitution G A intron_variant MELA-AU 18 77974629 77974629 single base substitution A C intron_variant MELA-AU 18 77975977 77975977 single base substitution G A intron_variant MELA-AU 18 77976543 77976543 single base substitution A C intron_variant MELA-AU 18 77976786 77976787 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 18 77976937 77976937 single base substitution G A intron_variant MELA-AU 18 77977172 77977172 single base substitution A G intron_variant MELA-AU 18 77977690 77977690 single base substitution G A intron_variant MELA-AU 18 77977779 77977779 single base substitution G A intron_variant MELA-AU 18 77978345 77978345 single base substitution G A intron_variant MELA-AU 18 77979281 77979281 single base substitution G A intron_variant MELA-AU 18 77980425 77980425 single base substitution G A intron_variant MELA-AU 18 77980739 77980739 single base substitution T C intron_variant MELA-AU 18 77980900 77980900 single base substitution G A intron_variant MELA-AU 18 77982625 77982625 single base substitution G A intron_variant MELA-AU 18 77983464 77983464 single base substitution A G intron_variant MELA-AU 18 77983790 77983790 single base substitution C T intron_variant MELA-AU 18 77984380 77984381 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 18 77984656 77984656 single base substitution G A intron_variant MELA-AU 18 77985164 77985164 insertion of <=200bp - T intron_variant MELA-AU 18 77985414 77985414 single base substitution G A intron_variant MELA-AU 18 77985915 77985915 single base substitution A G intron_variant MELA-AU 18 77986139 77986139 single base substitution C T intron_variant MELA-AU 18 77986584 77986584 single base substitution G A intron_variant MELA-AU 18 77987957 77987957 single base substitution C T intron_variant MELA-AU 18 77988412 77988412 single base substitution G A intron_variant MELA-AU 18 77989006 77989006 single base substitution G A intron_variant MELA-AU 18 77989370 77989370 single base substitution A G intron_variant MELA-AU 18 77990476 77990476 single base substitution G A intron_variant MELA-AU 18 77990718 77990718 single base substitution G A intron_variant MELA-AU 18 77991624 77991624 single base substitution G A intron_variant MELA-AU 18 77992494 77992494 single base substitution C A intron_variant MELA-AU 18 77993547 77993547 single base substitution A G intron_variant MELA-AU 18 77993723 77993723 single base substitution G A intron_variant MELA-AU 18 77993737 77993737 single base substitution A T intron_variant MELA-AU 18 77994426 77994426 single base substitution G A intron_variant MELA-AU 18 77994819 77994819 single base substitution A G intron_variant MELA-AU 18 77994826 77994826 single base substitution C T intron_variant MELA-AU 18 77994872 77994872 single base substitution G A intron_variant MELA-AU 18 77995493 77995493 single base substitution G A intron_variant MELA-AU 18 77995965 77995965 single base substitution G A intron_variant MELA-AU 18 77996272 77996272 single base substitution T G intron_variant MELA-AU 18 77996716 77996716 single base substitution G A intron_variant MELA-AU 18 77999455 77999455 single base substitution G A intron_variant MELA-AU 18 77999456 77999456 single base substitution G A intron_variant MELA-AU 18 77999529 77999529 single base substitution G A intron_variant MELA-AU 18 77999563 77999563 single base substitution G A intron_variant MELA-AU 18 78000528 78000528 single base substitution C T intron_variant MELA-AU 18 78000643 78000643 single base substitution G A intron_variant MELA-AU 18 78000674 78000674 single base substitution G A intron_variant MELA-AU 18 78001452 78001452 single base substitution G A intron_variant MELA-AU 18 78001661 78001661 single base substitution G A intron_variant MELA-AU 18 78001739 78001739 single base substitution G A intron_variant MELA-AU 18 78002138 78002139 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 18 78003377 78003377 single base substitution C T intron_variant MELA-AU 18 78003632 78003632 single base substitution C T intron_variant MELA-AU 18 78003959 78003959 single base substitution G A intron_variant MELA-AU 18 78005262 78005262 single base substitution C T 5_prime_UTR_variant MELA-AU 18 78005262 78005262 single base substitution C T upstream_gene_variant MELA-AU 18 78006114 78006114 single base substitution G A upstream_gene_variant MELA-AU 18 78006181 78006181 single base substitution C T upstream_gene_variant MELA-AU 18 78007125 78007125 single base substitution T G upstream_gene_variant MELA-AU 18 78008450 78008450 single base substitution G A upstream_gene_variant MELA-AU 18 78008486 78008486 single base substitution G A upstream_gene_variant MELA-AU 18 78008522 78008522 single base substitution C T upstream_gene_variant MELA-AU 18 78008841 78008841 single base substitution C T upstream_gene_variant ORCA-IN 18 77915398 77915398 single base substitution C T 3_prime_UTR_variant ORCA-IN 18 77935970 77935970 single base substitution T C downstream_gene_variant ORCA-IN 18 77935970 77935970 single base substitution T C intron_variant ORCA-IN 18 77954184 77954184 single base substitution G A intron_variant ORCA-IN 18 77959302 77959302 single base substitution C T intron_variant ORCA-IN 18 77964724 77964724 single base substitution A T intron_variant ORCA-IN 18 77964724 77964724 single base substitution A T upstream_gene_variant ORCA-IN 18 77971828 77971828 single base substitution T A intron_variant ORCA-IN 18 77973540 77973540 single base substitution G C intron_variant ORCA-IN 18 77977086 77977086 single base substitution G T intron_variant ORCA-IN 18 78009023 78009023 single base substitution T A upstream_gene_variant OV-AU 18 77914721 77914721 single base substitution C A downstream_gene_variant OV-AU 18 77916916 77916916 single base substitution G A 3_prime_UTR_variant OV-AU 18 77922549 77922549 single base substitution G A intron_variant OV-AU 18 77928060 77928060 single base substitution G C intron_variant OV-AU 18 77929013 77929013 single base substitution C G intron_variant OV-AU 18 77952551 77952551 single base substitution T A intron_variant OV-AU 18 77953694 77953694 single base substitution G A intron_variant OV-AU 18 77964290 77964290 single base substitution T A intron_variant OV-AU 18 77964290 77964290 single base substitution T A upstream_gene_variant OV-AU 18 77977385 77977385 single base substitution G A intron_variant OV-AU 18 77981110 77981110 single base substitution T C intron_variant OV-AU 18 77990876 77990876 single base substitution T C intron_variant OV-AU 18 77991038 77991038 single base substitution C T intron_variant OV-AU 18 77991728 77991728 single base substitution C A intron_variant OV-AU 18 77994147 77994147 single base substitution C G intron_variant OV-AU 18 77998414 77998414 single base substitution C G intron_variant OV-AU 18 77998985 77998985 single base substitution C G intron_variant OV-AU 18 78003246 78003246 single base substitution C T intron_variant PACA-AU 18 77911098 77911098 insertion of <=200bp - A downstream_gene_variant PACA-AU 18 77917708 77917708 single base substitution G C missense_variant S359R 1077C>G PACA-AU 18 77919018 77919018 single base substitution T A intron_variant PACA-AU 18 77922516 77922516 single base substitution T C intron_variant PACA-AU 18 77922533 77922533 single base substitution C G intron_variant PACA-AU 18 77923796 77923796 single base substitution C T intron_variant PACA-AU 18 77924379 77924379 single base substitution G A intron_variant PACA-AU 18 77926752 77926752 single base substitution G T intron_variant PACA-AU 18 77930856 77930856 insertion of <=200bp - A intron_variant PACA-AU 18 77930933 77930933 single base substitution G A intron_variant PACA-AU 18 77931262 77931262 single base substitution C A intron_variant PACA-AU 18 77935062 77935062 insertion of <=200bp - ACAT intron_variant PACA-AU 18 77936633 77936633 single base substitution G T downstream_gene_variant PACA-AU 18 77936633 77936633 single base substitution G T intron_variant PACA-AU 18 77940841 77940841 single base substitution C T 3_prime_UTR_variant PACA-AU 18 77940841 77940841 single base substitution C T intron_variant PACA-AU 18 77942392 77942392 single base substitution G T intron_variant PACA-AU 18 77947268 77947268 single base substitution G A intron_variant PACA-AU 18 77949671 77949671 single base substitution C A intron_variant PACA-AU 18 77951776 77951776 deletion of <=200bp A - intron_variant PACA-AU 18 77963156 77963156 single base substitution C T intron_variant PACA-AU 18 77963156 77963156 single base substitution C T upstream_gene_variant PACA-AU 18 77965791 77965791 single base substitution G T intron_variant PACA-AU 18 77965911 77965911 single base substitution C G intron_variant PACA-AU 18 77969788 77969788 single base substitution G A intron_variant PACA-AU 18 77972651 77972651 deletion of <=200bp A - intron_variant PACA-AU 18 77980412 77980412 single base substitution G C intron_variant PACA-AU 18 77982907 77982907 single base substitution C A intron_variant PACA-AU 18 77994285 77994285 single base substitution A G intron_variant PACA-AU 18 77996902 77996902 single base substitution C T intron_variant PACA-AU 18 77996953 77996953 single base substitution G A intron_variant PACA-AU 18 78001865 78001865 single base substitution A G intron_variant PACA-AU 18 78003735 78003735 deletion of <=200bp G - intron_variant PACA-AU 18 78004206 78004206 single base substitution A T intron_variant PACA-AU 18 78004890 78004902 deletion of <=200bp CCGCGGAGCGGGT - intron_variant PACA-AU 18 78008742 78008742 single base substitution A G upstream_gene_variant PACA-CA 18 77911782 77911782 single base substitution C A downstream_gene_variant PACA-CA 18 77915369 77915369 single base substitution G A 3_prime_UTR_variant PACA-CA 18 77917707 77917707 single base substitution G A synonymous_variant L360L 1078C>T PACA-CA 18 77918298 77918298 single base substitution G A missense_variant R163W 487C>T PACA-CA 18 77919312 77919312 single base substitution T C intron_variant PACA-CA 18 77921345 77921345 single base substitution C G intron_variant PACA-CA 18 77924403 77924403 single base substitution T G intron_variant PACA-CA 18 77926795 77926795 insertion of <=200bp - ACAAATAAC intron_variant PACA-CA 18 77929078 77929078 single base substitution G A intron_variant PACA-CA 18 77930520 77930520 single base substitution G A intron_variant PACA-CA 18 77935303 77935303 single base substitution C T intron_variant PACA-CA 18 77935349 77935349 single base substitution C T intron_variant PACA-CA 18 77936842 77936842 single base substitution G C downstream_gene_variant PACA-CA 18 77936842 77936842 single base substitution G C intron_variant PACA-CA 18 77937864 77937864 single base substitution C T downstream_gene_variant PACA-CA 18 77937864 77937864 single base substitution C T intron_variant PACA-CA 18 77940431 77940431 single base substitution G A downstream_gene_variant PACA-CA 18 77940431 77940431 single base substitution G A intron_variant PACA-CA 18 77943936 77943936 single base substitution C A intron_variant PACA-CA 18 77944053 77944053 single base substitution G A intron_variant PACA-CA 18 77944723 77944723 single base substitution C T intron_variant PACA-CA 18 77945545 77945545 single base substitution G A intron_variant PACA-CA 18 77949090 77949090 single base substitution G A intron_variant PACA-CA 18 77950070 77950070 single base substitution G A intron_variant PACA-CA 18 77951044 77951044 single base substitution G A intron_variant PACA-CA 18 77951891 77951891 deletion of <=200bp A - intron_variant PACA-CA 18 77952879 77952879 single base substitution A G intron_variant PACA-CA 18 77956616 77956616 single base substitution C G intron_variant PACA-CA 18 77956778 77956778 single base substitution C T intron_variant PACA-CA 18 77961016 77961016 single base substitution T A intron_variant PACA-CA 18 77961016 77961016 single base substitution T A upstream_gene_variant PACA-CA 18 77961929 77961929 single base substitution G A intron_variant PACA-CA 18 77961929 77961929 single base substitution G A upstream_gene_variant PACA-CA 18 77964318 77964318 single base substitution C A intron_variant PACA-CA 18 77964318 77964318 single base substitution C A upstream_gene_variant PACA-CA 18 77965350 77965350 single base substitution C T intron_variant PACA-CA 18 77965350 77965350 single base substitution C T upstream_gene_variant PACA-CA 18 77966844 77966844 single base substitution G A intron_variant PACA-CA 18 77970614 77970614 deletion of <=200bp A - intron_variant PACA-CA 18 77971167 77971167 single base substitution A T intron_variant PACA-CA 18 77971173 77971173 single base substitution C T intron_variant PACA-CA 18 77971822 77971822 single base substitution T C intron_variant PACA-CA 18 77972006 77972006 single base substitution G T intron_variant PACA-CA 18 77972813 77972813 deletion of <=200bp A - intron_variant PACA-CA 18 77974156 77974156 single base substitution A C intron_variant PACA-CA 18 77980499 77980499 single base substitution C T intron_variant PACA-CA 18 77982235 77982235 single base substitution T C intron_variant PACA-CA 18 77991386 77991386 single base substitution A T intron_variant PACA-CA 18 77992254 77992254 single base substitution C A intron_variant PACA-CA 18 77996223 77996223 single base substitution G T intron_variant PACA-CA 18 77996721 77996721 single base substitution G C intron_variant PACA-CA 18 77999047 77999047 single base substitution T C intron_variant PACA-CA 18 78008357 78008357 single base substitution G C upstream_gene_variant PACA-CA 18 78009376 78009376 single base substitution G A upstream_gene_variant PAEN-AU 18 77970732 77970732 single base substitution C A intron_variant PAEN-AU 18 78000909 78000909 single base substitution T C intron_variant PAEN-IT 18 77927423 77927423 single base substitution C T intron_variant PAEN-IT 18 77959704 77959704 single base substitution C A intron_variant PAEN-IT 18 77987979 77987979 single base substitution C T intron_variant PAEN-IT 18 77994490 77994490 single base substitution C A intron_variant PBCA-DE 18 77913805 77913805 single base substitution G A downstream_gene_variant PBCA-DE 18 77919519 77919519 single base substitution C G intron_variant PBCA-DE 18 77920319 77920319 single base substitution G A intron_variant PBCA-DE 18 77927210 77927210 single base substitution C T intron_variant PBCA-DE 18 77934905 77934905 single base substitution C T intron_variant PBCA-DE 18 77934907 77934907 single base substitution T C intron_variant PBCA-DE 18 77935245 77935246 deletion of <=200bp AC - intron_variant PBCA-DE 18 77939521 77939521 single base substitution C T downstream_gene_variant PBCA-DE 18 77939521 77939521 single base substitution C T intron_variant PBCA-DE 18 77943878 77943878 single base substitution G C intron_variant PBCA-DE 18 77953432 77953433 deletion of <=200bp AT - intron_variant PBCA-DE 18 77960842 77960842 single base substitution G A intron_variant PBCA-DE 18 77960842 77960842 single base substitution G A upstream_gene_variant PBCA-DE 18 77974341 77974341 single base substitution A T intron_variant PBCA-DE 18 77980117 77980117 single base substitution G A intron_variant PBCA-DE 18 77992082 77992082 single base substitution C A intron_variant PBCA-DE 18 78003251 78003251 single base substitution T C intron_variant PBCA-DE 18 78009913 78009913 single base substitution C T upstream_gene_variant PBCA-DE 18 78010311 78010311 single base substitution C A upstream_gene_variant PBCA-DE 18 78010363 78010363 single base substitution G A upstream_gene_variant PRAD-CA 18 77932579 77932579 single base substitution T G intron_variant PRAD-CA 18 77935185 77935185 single base substitution G T intron_variant PRAD-CA 18 77958907 77958907 single base substitution C T intron_variant PRAD-UK 18 77920882 77920882 single base substitution C T intron_variant PRAD-UK 18 77922962 77922962 single base substitution C T intron_variant PRAD-UK 18 77929153 77929153 single base substitution T C intron_variant PRAD-UK 18 77933201 77933201 single base substitution T A intron_variant PRAD-UK 18 77945784 77945784 single base substitution C T intron_variant PRAD-UK 18 77975974 77975974 single base substitution G A intron_variant PRAD-UK 18 77993712 77993712 single base substitution T C intron_variant RECA-EU 18 77920506 77920506 single base substitution G A intron_variant RECA-EU 18 77928057 77928057 single base substitution A C intron_variant RECA-EU 18 77948339 77948339 single base substitution C A intron_variant RECA-EU 18 77957976 77957976 single base substitution G A intron_variant RECA-EU 18 77960012 77960012 single base substitution C T intron_variant RECA-EU 18 77966876 77966876 single base substitution G C intron_variant RECA-EU 18 77974898 77974898 single base substitution G A intron_variant RECA-EU 18 77988658 77988658 single base substitution G A intron_variant RECA-EU 18 78006076 78006076 single base substitution A T upstream_gene_variant RECA-EU 18 78006265 78006265 single base substitution A T upstream_gene_variant SKCA-BR 18 77912250 77912250 single base substitution C A downstream_gene_variant SKCA-BR 18 77912313 77912313 single base substitution C T downstream_gene_variant SKCA-BR 18 77912332 77912332 single base substitution C A downstream_gene_variant SKCA-BR 18 77912402 77912402 single base substitution C T downstream_gene_variant SKCA-BR 18 77912427 77912427 single base substitution C G downstream_gene_variant SKCA-BR 18 77912445 77912445 single base substitution C G downstream_gene_variant SKCA-BR 18 77912463 77912463 single base substitution C G downstream_gene_variant SKCA-BR 18 77912513 77912513 single base substitution C A downstream_gene_variant SKCA-BR 18 77913699 77913699 single base substitution C T downstream_gene_variant SKCA-BR 18 77913700 77913700 single base substitution C T downstream_gene_variant SKCA-BR 18 77917789 77917789 single base substitution C A synonymous_variant A332A 996G>T SKCA-BR 18 77917951 77917951 single base substitution A G synonymous_variant G278G 834T>C SKCA-BR 18 77919426 77919426 single base substitution G A intron_variant SKCA-BR 18 77923580 77923580 single base substitution T A intron_variant SKCA-BR 18 77925899 77925899 single base substitution G A intron_variant SKCA-BR 18 77925900 77925900 single base substitution G A intron_variant SKCA-BR 18 77926456 77926458 deletion of <=200bp TTG - intron_variant SKCA-BR 18 77938454 77938454 single base substitution A T downstream_gene_variant SKCA-BR 18 77938454 77938454 single base substitution A T intron_variant SKCA-BR 18 77938455 77938455 single base substitution C T downstream_gene_variant SKCA-BR 18 77938455 77938455 single base substitution C T intron_variant SKCA-BR 18 77939154 77939154 single base substitution G A downstream_gene_variant SKCA-BR 18 77939154 77939154 single base substitution G A intron_variant SKCA-BR 18 77939695 77939695 single base substitution C T downstream_gene_variant SKCA-BR 18 77939695 77939695 single base substitution C T intron_variant SKCA-BR 18 77942415 77942415 single base substitution C T intron_variant SKCA-BR 18 77943878 77943878 single base substitution G C intron_variant SKCA-BR 18 77945280 77945280 insertion of <=200bp - CGT intron_variant SKCA-BR 18 77946141 77946141 single base substitution C T intron_variant SKCA-BR 18 77953453 77953457 deletion of <=200bp TATAC - intron_variant SKCA-BR 18 77953457 77953457 single base substitution C T intron_variant SKCA-BR 18 77953816 77953816 single base substitution A G intron_variant SKCA-BR 18 77954746 77954746 single base substitution G A intron_variant SKCA-BR 18 77955804 77955804 single base substitution C T intron_variant SKCA-BR 18 77961074 77961074 single base substitution G A intron_variant SKCA-BR 18 77961074 77961074 single base substitution G A upstream_gene_variant SKCA-BR 18 77964624 77964624 single base substitution C T intron_variant SKCA-BR 18 77964624 77964624 single base substitution C T upstream_gene_variant SKCA-BR 18 77968608 77968608 single base substitution A C intron_variant SKCA-BR 18 77969977 77969977 single base substitution G A intron_variant SKCA-BR 18 77971049 77971049 single base substitution A G intron_variant SKCA-BR 18 77974555 77974555 single base substitution T A intron_variant SKCA-BR 18 77977993 77977993 single base substitution T A intron_variant SKCA-BR 18 77980645 77980645 single base substitution C T intron_variant SKCA-BR 18 77982534 77982534 single base substitution A T intron_variant SKCA-BR 18 77984039 77984039 insertion of <=200bp - TTTG intron_variant SKCA-BR 18 77990413 77990413 single base substitution G A intron_variant SKCA-BR 18 77996510 77996510 single base substitution C T intron_variant SKCA-BR 18 77996750 77996750 single base substitution C G intron_variant SKCA-BR 18 78001820 78001820 single base substitution G A intron_variant SKCA-BR 18 78003807 78003807 single base substitution A C intron_variant SKCA-BR 18 78004739 78004739 single base substitution G A intron_variant SKCA-BR 18 78005488 78005488 single base substitution G C upstream_gene_variant SKCA-BR 18 78008082 78008082 single base substitution T A upstream_gene_variant SKCA-BR 18 78008273 78008274 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 18 78010130 78010130 single base substitution C T upstream_gene_variant SKCM-US 18 77918229 77918229 single base substitution C T missense_variant G186R 556G>A STAD-US 18 77917915 77917915 deletion of <=200bp G - frameshift_variant P290 STAD-US 18 77917966 77917966 single base substitution G A synonymous_variant T273T 819C>T STAD-US 18 77917987 77917987 single base substitution C T synonymous_variant S266S 798G>A STAD-US 18 77918087 77918087 single base substitution G A missense_variant T233M 698C>T STAD-US 18 77918110 77918110 single base substitution G A synonymous_variant A225A 675C>T STAD-US 18 77918406 77918406 deletion of <=200bp G - frameshift_variant R127 STAD-US 18 77960807 77960807 single base substitution C T synonymous_variant A27A 81G>A STAD-US 18 77960807 77960807 single base substitution C T upstream_gene_variant THCA-SA 18 77916382 77916382 single base substitution T C 3_prime_UTR_variant THCA-SA 18 77926862 77926862 single base substitution G A intron_variant THCA-SA 18 77936214 77936214 single base substitution G A downstream_gene_variant THCA-SA 18 77936214 77936214 single base substitution G A intron_variant UCEC-US 18 78005221 78005221 single base substitution C A missense_variant S4I 11G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T207 COSM4711137 c.418T>G p.F140V Substitution - Missense 18:80160484-80160484 - TCGA-G4-6309-01 COSM1389890 c.464C>T p.T155M Substitution - Missense 18:80160438-80160438 - BD236T COSM5519565 c.544G>A p.V182M Substitution - Missense 18:80160358-80160358 - DLD1 COSM1680441 c.217C>T p.P73S Substitution - Missense 18:80202788-80202788 - TCGA-EK-A2RC-01 COSM4848461 c.438C>T p.I146I Substitution - coding silent 18:80160464-80160464 - TCGA-BR-8363-01 COSM4073534 c.675C>T p.A225A Substitution - coding silent 18:80160227-80160227 - sysucc-311T COSM5464365 c.910G>A p.E304K Substitution - Missense 18:80159992-80159992 - SJOS001107_M2 COSM5023414 c.134T>C p.F45S Substitution - Missense 18:80202871-80202871 - J90_T COSM3959428 c.1087C>T p.P363S Substitution - Missense 18:80159815-80159815 - TCGA-EE-A20C-06 COSM3527851 c.556G>A p.G186R Substitution - Missense 18:80160346-80160346 - T3090 COSM4711136 c.542G>A p.R181H Substitution - Missense 18:80160360-80160360 - ESCC_BICR_054T COSM5444245 c.165C>G p.I55M Substitution - Missense 18:80202840-80202840 - 587278 COSM1219286 c.712G>A p.A238T Substitution - Missense 18:80160190-80160190 - Gp2D COSM4627610 c.847C>T p.R283C Substitution - Missense 18:80160055-80160055 - 8057501 COSM3388517 c.1077C>G p.S359R Substitution - Missense 18:80159825-80159825 - sysucc-834T COSM5485968 c.588G>A p.S196S Substitution - coding silent 18:80160314-80160314 - HCT-15 COSM1680441 c.217C>T p.P73S Substitution - Missense 18:80202788-80202788 - RH18C COSM4985088 c.1061C>G p.A354G Substitution - Missense 18:80159841-80159841 - C70 COSM4619470 c.804G>A p.P268P Substitution - coding silent 18:80160098-80160098 - PCSI_0341_Pa_P_526 COSM4807937 c.487C>T p.R163W Substitution - Missense 18:80160415-80160415 - cSCCP7 COSM140182 c.3G>A p.M1I Substitution - Missense 18:80247346-80247346 - TCGA-CM-4743-01 COSM1389888 c.940delC p.Q314fs*>63 Deletion - Frameshift 18:80159962-80159962 - ATL023 COSM5706820 c.196G>A p.D66N Substitution - Missense 18:80202809-80202809 - P146 COSM1737182 c.532G>A p.A178T Substitution - Missense 18:80160370-80160370 - SJOS001107_M1 COSM5023414 c.134T>C p.F45S Substitution - Missense 18:80202871-80202871 - B110 COSM1750597 c.677G>A p.G226E Substitution - Missense 18:80160225-80160225 - TCGA-F1-6177-01 COSM4073533 c.698C>T p.T233M Substitution - Missense 18:80160204-80160204 - CHC2208T COSM4953167 c.1072C>T p.H358Y Substitution - Missense 18:80159830-80159830 - HCT15 COSM1680441 c.217C>T p.P73S Substitution - Missense 18:80202788-80202788 - LUAD-CHTN-MAD08-00104 COSM361193 c.68G>A p.S23N Substitution - Missense 18:80247281-80247281 - HCC122T COSM5808586 c.230A>G p.D77G Substitution - Missense 18:80202775-80202775 - SW1417 COSM3147688 c.791G>A p.G264D Substitution - Missense 18:80160111-80160111 - T2197 COSM4711138 c.415G>A p.D139N Substitution - Missense 18:80160487-80160487 - T1194 COSM4711139 c.330G>A p.S110S Substitution - coding silent 18:80160572-80160572 - TCGA-BR-8487-01 COSM4073535 c.81G>A p.A27A Substitution - coding silent 18:80202924-80202924 - TCGA-D5-6531-01 COSM3692215 c.705G>T p.M235I Substitution - Missense 18:80160197-80160197 - CHC302T COSM5347726 c.775_779delGGCGG p.G259fs*37 Deletion - Frameshift 18:80160123-80160127 - TCGA-D1-A17Q-01 COSM990139 c.11G>T p.S4I Substitution - Missense 18:80247338-80247338 - HN_62505 COSM125133 c.383G>T p.R128L Substitution - Missense 18:80160519-80160519 - BD114T COSM5504422 c.213G>C p.L71L Substitution - coding silent 18:80202792-80202792 - B110-Tumor COSM1750597 c.677G>A p.G226E Substitution - Missense 18:80160225-80160225 - BD57T COSM5510973 c.901G>A p.V301I Substitution - Missense 18:80160001-80160001 - TCGA-BR-8591-01 COSM4073531 c.819C>T p.T273T Substitution - coding silent 18:80160083-80160083 - TCGA-BR-8382-01 COSM4073532 c.798G>A p.S266S Substitution - coding silent 18:80160104-80160104 - B74-Tumor COSM1750598 c.629T>C p.L210P Substitution - Missense 18:80160273-80160273 - CHC2208T COSM4953167 c.1072C>T p.H358Y Substitution - Missense 18:80159830-80159830 - CSCC-20-T COSM4508668 c.783C>T p.R261R Substitution - coding silent 18:80160119-80160119 - HCC2998 COSM3147693 c.87C>T p.F29F Substitution - coding silent 18:80202918-80202918 - 90203 COSM330361 c.153C>A p.H51Q Substitution - Missense 18:80202852-80202852 - T18 COSM5618971 c.564G>A p.E188E Substitution - coding silent 18:80160338-80160338 - LUAD-RT-S01840 COSM384771 c.674C>T p.A225V Substitution - Missense 18:80160228-80160228 - TCGA-G2-A2EO-01 COSM1303883 c.850G>A p.V284I Substitution - Missense 18:80160052-80160052 - TCGA-06-0877-01 COSM3403687 c.411G>A p.P137P Substitution - coding silent 18:80160491-80160491 - TCGA-G4-6586-01 COSM1219286 c.712G>A p.A238T Substitution - Missense 18:80160190-80160190 - TCGA-AC-A5XS-01 COSM4391286 c.1077C>T p.S359S Substitution - coding silent 18:80159825-80159825 - CHC322T COSM3668147 c.879G>T p.A293A Substitution - coding silent 18:80160023-80160023 - TCGA-34-2600-01 COSM708798 c.256A>G p.S86G Substitution - Missense 18:80202749-80202749 - TCGA-Q1-A73O-01 COSM4836201 c.1047C>T p.L349L Substitution - coding silent 18:80159855-80159855 - TCGA-AG-3893-01 COSM288763 c.95T>C p.F32S Substitution - Missense 18:80202910-80202910 - 15 COSM5733033 c.413G>A p.R138H Substitution - Missense 18:80160489-80160489 - ESO-0292 COSM1241546 c.757C>T p.R253C Substitution - Missense 18:80160145-80160145 - T2 COSM5618971 c.564G>A p.E188E Substitution - coding silent 18:80160338-80160338 - 19 COSM5747951 c.940_941insC p.Q314fs*>64 Insertion - Frameshift 18:80159961-80159962 - ESCC_60 COSM5632717 c.490C>T p.H164Y Substitution - Missense 18:80160412-80160412 - TCGA-CM-6168-01 COSM1389891 c.127G>C p.E43Q Substitution - Missense 18:80202878-80202878 - 424 COSM4432612 c.579C>A p.I193I Substitution - coding silent 18:80160323-80160323 - PCSI_0611_Pa_P_526 COSM5761784 c.1078C>T p.L360L Substitution - coding silent 18:80159824-80159824 - sysucc-880T COSM5462777 c.507G>A p.P169P Substitution - coding silent 18:80160395-80160395 - B74 COSM1750598 c.629T>C p.L210P Substitution - Missense 18:80160273-80160273 - CHC322T COSM3668147 c.879G>T p.A293A Substitution - coding silent 18:80160023-80160023 - ESCC_158 COSM1737182 c.532G>A p.A178T Substitution - Missense 18:80160370-80160370 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.654913;Hs.654915;Hs.654917;Hs.654918;Hs.654920 18q23 608976 2469858|CGAP|BC060797|A/G|non-coding||2228|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.F32S c.95T>C 18 77960793 COREAD C A Missense p.R128L c.383G>T 18 77918402 HNSC CC TT Missense p.G165N c.493_494delinsAA 18 77918291 CM C T Missense p.A318T c.952G>A 18 77917833 HNSC C T Missense p.G186R c.556G>A 18 77918229 CM C T Missense p.V284I c.850G>A 18 77917935 BLCA G A Missense p.S270L c.809C>T 18 77917976 HNSC G A Missense p.T233M c.698C>T 18 77918087 STAD G A Synonymous p.I74I c.222C>T 18 77960666 HNSC GG AA Missense p.P313L c.938_939delinsTT 18 77917846 CM T C Missense p.S86G c.256A>G 18 77960632 LUSC