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 11 63764070 63764070 + Silent SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr11:63764070C>T c.288C>T c.(286-288)ttC>ttT p.F96F BLCA 11 63764545 63764545 + Silent SNP G G A TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr11:63764545G>A c.447G>A c.(445-447)gtG>gtA p.V149V BLCA 11 63764993 63764993 + Missense_Mutation SNP G G C TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr11:63764993G>C c.791G>C c.(790-792)gGa>gCa p.G264A BRCA 11 63764394 63764394 + Missense_Mutation SNP T T C TCGA-D8-A27L-01A-11D-A16D-09 TCGA-D8-A27L-10A-01D-A16D-09 g.chr11:63764394T>C c.404T>C c.(403-405)aTt>aCt p.I135T COAD 11 63764062 63764062 + Missense_Mutation SNP C C T TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr11:63764062C>T c.280C>T c.(280-282)Cgg>Tgg p.R94W COAD 11 63764063 63764063 + Missense_Mutation SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr11:63764063G>A c.281G>A c.(280-282)cGg>cAg p.R94Q COAD 11 63764561 63764561 + Missense_Mutation SNP G G C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:63764561G>C c.463G>C c.(463-465)Gtc>Ctc p.V155L COAD 11 63764690 63764690 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:63764690C>T c.592C>T c.(592-594)Cgg>Tgg p.R198W COADREAD 11 63764062 63764062 + Missense_Mutation SNP C C T TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr11:63764062C>T c.280C>T c.(280-282)Cgg>Tgg p.R94W COADREAD 11 63764063 63764063 + Missense_Mutation SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr11:63764063G>A c.281G>A c.(280-282)cGg>cAg p.R94Q COADREAD 11 63764561 63764561 + Missense_Mutation SNP G G C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:63764561G>C c.463G>C c.(463-465)Gtc>Ctc p.V155L COADREAD 11 63764690 63764690 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:63764690C>T c.592C>T c.(592-594)Cgg>Tgg p.R198W ESCA 11 63764925 63764925 + Silent SNP C C T TCGA-L5-A8NH-01A-11D-A37C-09 TCGA-L5-A8NH-11A-11D-A37F-09 g.chr11:63764925C>T c.723C>T c.(721-723)ggC>ggT p.G241G GBMLGG 11 63764577 63764579 + In_Frame_Del DEL CCT CCT - TCGA-HT-7694-01A-11D-2253-08 TCGA-HT-7694-10A-01D-2253-08 g.chr11:63764577_63764579delCCT c.479_481delCCT c.(478-483)gcctcc>gcc p.S161del HNSC 11 63764101 63764101 + Missense_Mutation SNP G G A TCGA-CQ-5326-01A-01D-1870-08 TCGA-CQ-5326-10A-01D-1870-08 g.chr11:63764101G>A c.319G>A c.(319-321)Gac>Aac p.D107N HNSC 11 63764862 63764862 + Silent SNP C C T TCGA-CV-A6JM-01A-11D-A31L-08 TCGA-CV-A6JM-10A-01D-A31J-08 g.chr11:63764862C>T c.660C>T c.(658-660)atC>atT p.I220I KICH 11 63756163 63756163 + Missense_Mutation SNP A A G TCGA-KN-8437-01A-11D-2310-10 TCGA-KN-8437-11A-01D-2311-10 g.chr11:63756163A>G c.158A>G c.(157-159)gAg>gGg p.E53G KIPAN 11 63756155 63756155 + Missense_Mutation SNP G G T TCGA-B9-4115-01A-01D-1252-08 TCGA-B9-4115-10A-01D-1252-08 g.chr11:63756155G>T c.150G>T c.(148-150)gaG>gaT p.E50D KIPAN 11 63756163 63756163 + Missense_Mutation SNP A A G TCGA-KN-8437-01A-11D-2310-10 TCGA-KN-8437-11A-01D-2311-10 g.chr11:63756163A>G c.158A>G c.(157-159)gAg>gGg p.E53G KIPAN 11 63764641 63764641 + Silent SNP C C A TCGA-CJ-4882-01A-02D-1429-08 TCGA-CJ-4882-11A-01D-1429-08 g.chr11:63764641C>A c.543C>A c.(541-543)ggC>ggA p.G181G KIRC 11 63764641 63764641 + Silent SNP C C A TCGA-CJ-4882-01A-02D-1429-08 TCGA-CJ-4882-11A-01D-1429-08 g.chr11:63764641C>A c.543C>A c.(541-543)ggC>ggA p.G181G KIRP 11 63756155 63756155 + Missense_Mutation SNP G G T TCGA-B9-4115-01A-01D-1252-08 TCGA-B9-4115-10A-01D-1252-08 g.chr11:63756155G>T c.150G>T c.(148-150)gaG>gaT p.E50D LGG 11 63764577 63764579 + In_Frame_Del DEL CCT CCT - TCGA-HT-7694-01A-11D-2253-08 TCGA-HT-7694-10A-01D-2253-08 g.chr11:63764577_63764579delCCT c.479_481delCCT c.(478-483)gcctcc>gcc p.S161del LIHC 11 63753947 63753947 + Nonsense_Mutation SNP C C T TCGA-5R-AA1D-01A-11D-A382-10 TCGA-5R-AA1D-10A-01D-A385-10 g.chr11:63753947C>T c.19C>T c.(19-21)Cag>Tag p.Q7* LIHC 11 63764415 63764415 + Splice_Site SNP T T C TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr11:63764415T>C c.e5+2 LIHC 11 63765004 63765004 + Missense_Mutation SNP A A G TCGA-DD-AAD6-01A-11D-A40R-10 TCGA-DD-AAD6-10A-01D-A40U-10 g.chr11:63765004A>G c.802A>G c.(802-804)Atc>Gtc p.I268V LUAD 11 63764060 63764060 + Missense_Mutation SNP A A G TCGA-55-7573-01A-11D-2036-08 TCGA-55-7573-11A-01D-2036-08 g.chr11:63764060A>G c.278A>G c.(277-279)tAt>tGt p.Y93C LUSC 11 63764701 63764701 + Frame_Shift_Del DEL G G - TCGA-66-2765-01A-01D-1522-08 TCGA-66-2765-11A-01D-1522-08 g.chr11:63764701delG c.603delG c.(601-603)aagfs p.K201fs PRAD 11 63764357 63764357 + Nonsense_Mutation SNP G G T TCGA-HC-7750-01A-11D-2114-08 TCGA-HC-7750-10A-01D-2115-08 g.chr11:63764357G>T c.367G>T c.(367-369)Gaa>Taa p.E123* SARC 11 63764938 63764938 + Missense_Mutation SNP C C G TCGA-IF-A4AJ-01A-11D-A24N-09 TCGA-IF-A4AJ-11A-12D-A24N-09 g.chr11:63764938C>G c.736C>G c.(736-738)Ccg>Gcg p.P246A SARC 11 63764973 63764973 + Silent SNP C C T TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chr11:63764973C>T c.771C>T c.(769-771)gtC>gtT p.V257V SKCM 11 63764603 63764603 + Missense_Mutation SNP G G A TCGA-EE-A29G-06A-12D-A196-08 TCGA-EE-A29G-10A-01D-A198-08 g.chr11:63764603G>A c.505G>A c.(505-507)Gac>Aac p.D169N SKCM 11 63764668 63764668 + Silent SNP C C T TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr11:63764668C>T c.570C>T c.(568-570)ttC>ttT p.F190F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BRCA-EU 11 63749113 63749113 single base substitution A G upstream_gene_variant BRCA-EU 11 63749412 63749412 single base substitution A G upstream_gene_variant BRCA-EU 11 63750730 63750730 single base substitution G A upstream_gene_variant BRCA-EU 11 63750812 63750812 single base substitution C G upstream_gene_variant BRCA-EU 11 63753267 63753267 single base substitution C T upstream_gene_variant BRCA-EU 11 63755290 63755290 single base substitution G C intron_variant BRCA-EU 11 63756790 63756790 single base substitution A C exon_variant BRCA-EU 11 63756790 63756790 single base substitution A C intron_variant BRCA-EU 11 63756866 63756866 single base substitution C G exon_variant BRCA-EU 11 63756866 63756866 single base substitution C G intron_variant BRCA-EU 11 63757703 63757703 single base substitution C T exon_variant BRCA-EU 11 63757703 63757703 single base substitution C T intron_variant BRCA-EU 11 63760003 63760003 single base substitution G A downstream_gene_variant BRCA-EU 11 63760003 63760003 single base substitution G A intron_variant BRCA-EU 11 63760415 63760415 single base substitution C T downstream_gene_variant BRCA-EU 11 63760415 63760415 single base substitution C T intron_variant BRCA-EU 11 63761087 63761087 single base substitution G T downstream_gene_variant BRCA-EU 11 63761087 63761087 single base substitution G T intron_variant BRCA-EU 11 63761428 63761428 single base substitution G A downstream_gene_variant BRCA-EU 11 63761428 63761428 single base substitution G A intron_variant BRCA-EU 11 63761747 63761747 single base substitution C G downstream_gene_variant BRCA-EU 11 63761747 63761747 single base substitution C G intron_variant BRCA-EU 11 63763957 63763957 single base substitution G A intron_variant BRCA-EU 11 63763957 63763957 single base substitution G A upstream_gene_variant BRCA-EU 11 63764920 63764920 single base substitution G A downstream_gene_variant BRCA-EU 11 63764920 63764920 single base substitution G A exon_variant BRCA-EU 11 63764920 63764920 single base substitution G A intron_variant BRCA-EU 11 63764920 63764920 single base substitution G A missense_variant E139K 415G>A BRCA-EU 11 63764920 63764920 single base substitution G A missense_variant E210K 628G>A BRCA-EU 11 63764920 63764920 single base substitution G A missense_variant E240K 718G>A BRCA-EU 11 63764920 63764920 single base substitution G A missense_variant E249K 745G>A BRCA-EU 11 63764920 63764920 single base substitution G A missense_variant E277K 829G>A BRCA-EU 11 63764920 63764920 single base substitution G A upstream_gene_variant BRCA-EU 11 63765233 63765233 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 63765233 63765233 single base substitution C T downstream_gene_variant BRCA-EU 11 63765233 63765233 single base substitution C T exon_variant BRCA-EU 11 63765233 63765233 single base substitution C T synonymous_variant L257L 771C>T BRCA-EU 11 63765233 63765233 single base substitution C T upstream_gene_variant BRCA-EU 11 63766574 63766574 single base substitution T A downstream_gene_variant BRCA-EU 11 63766574 63766574 single base substitution T A intron_variant BRCA-EU 11 63766574 63766574 single base substitution T A upstream_gene_variant BRCA-EU 11 63767390 63767390 single base substitution C G downstream_gene_variant BRCA-EU 11 63767390 63767390 single base substitution C G intron_variant BRCA-EU 11 63767390 63767390 single base substitution C G upstream_gene_variant BRCA-EU 11 63768393 63768393 single base substitution G C downstream_gene_variant BRCA-EU 11 63768393 63768393 single base substitution G C intron_variant BRCA-EU 11 63768393 63768393 single base substitution G C upstream_gene_variant BRCA-EU 11 63768492 63768492 single base substitution G C downstream_gene_variant BRCA-EU 11 63768492 63768492 single base substitution G C intron_variant BRCA-EU 11 63768492 63768492 single base substitution G C upstream_gene_variant BRCA-EU 11 63768561 63768561 single base substitution G A downstream_gene_variant BRCA-EU 11 63768561 63768561 single base substitution G A intron_variant BRCA-EU 11 63768561 63768561 single base substitution G A upstream_gene_variant BRCA-EU 11 63769909 63769909 single base substitution G C downstream_gene_variant BRCA-EU 11 63770669 63770669 single base substitution T C downstream_gene_variant BRCA-EU 11 63771960 63771960 single base substitution A C downstream_gene_variant BRCA-EU 11 63772661 63772661 single base substitution C T downstream_gene_variant BRCA-EU 11 63773007 63773007 single base substitution G T downstream_gene_variant BRCA-EU 11 63773517 63773517 single base substitution G T downstream_gene_variant BRCA-EU 11 63773957 63773957 single base substitution G A downstream_gene_variant BRCA-EU 11 63773964 63773964 single base substitution G A downstream_gene_variant BRCA-EU 11 63773981 63773981 single base substitution G A downstream_gene_variant BRCA-FR 11 63756790 63756790 single base substitution A C exon_variant BRCA-FR 11 63756790 63756790 single base substitution A C intron_variant BRCA-FR 11 63757703 63757703 single base substitution C T exon_variant BRCA-FR 11 63757703 63757703 single base substitution C T intron_variant BRCA-FR 11 63761087 63761087 single base substitution G T downstream_gene_variant BRCA-FR 11 63761087 63761087 single base substitution G T intron_variant BRCA-FR 11 63764986 63764986 single base substitution C T downstream_gene_variant BRCA-FR 11 63764986 63764986 single base substitution C T exon_variant BRCA-FR 11 63764986 63764986 single base substitution C T intron_variant BRCA-FR 11 63764986 63764986 single base substitution C T missense_variant R161W 481C>T BRCA-FR 11 63764986 63764986 single base substitution C T missense_variant R232W 694C>T BRCA-FR 11 63764986 63764986 single base substitution C T missense_variant R262W 784C>T BRCA-FR 11 63764986 63764986 single base substitution C T missense_variant R271W 811C>T BRCA-FR 11 63764986 63764986 single base substitution C T missense_variant R299W 895C>T BRCA-FR 11 63764986 63764986 single base substitution C T upstream_gene_variant BRCA-FR 11 63768393 63768393 single base substitution G C downstream_gene_variant BRCA-FR 11 63768393 63768393 single base substitution G C intron_variant BRCA-FR 11 63768393 63768393 single base substitution G C upstream_gene_variant BRCA-FR 11 63768492 63768492 single base substitution G C downstream_gene_variant BRCA-FR 11 63768492 63768492 single base substitution G C intron_variant BRCA-FR 11 63768492 63768492 single base substitution G C upstream_gene_variant BRCA-FR 11 63773517 63773517 single base substitution G T downstream_gene_variant BRCA-FR 11 63773957 63773957 single base substitution G A downstream_gene_variant BRCA-FR 11 63773964 63773964 single base substitution G A downstream_gene_variant BRCA-US 11 63753882 63753882 single base substitution G C 5_prime_UTR_variant BRCA-US 11 63753882 63753882 single base substitution G C exon_variant BRCA-US 11 63753882 63753882 single base substitution G C missense_variant R22P 65G>C BRCA-US 11 63753882 63753882 single base substitution G C upstream_gene_variant BRCA-US 11 63764394 63764394 single base substitution T C exon_variant BRCA-US 11 63764394 63764394 single base substitution T C intron_variant BRCA-US 11 63764394 63764394 single base substitution T C missense_variant I105T 314T>C BRCA-US 11 63764394 63764394 single base substitution T C missense_variant I135T 404T>C BRCA-US 11 63764394 63764394 single base substitution T C missense_variant I144T 431T>C BRCA-US 11 63764394 63764394 single base substitution T C missense_variant I172T 515T>C BRCA-US 11 63764394 63764394 single base substitution T C upstream_gene_variant BRCA-US 11 63767714 63767714 single base substitution G C downstream_gene_variant BRCA-US 11 63767714 63767714 single base substitution G C intron_variant BRCA-US 11 63767714 63767714 single base substitution G C upstream_gene_variant BTCA-JP 11 63756016 63756016 single base substitution G A exon_variant BTCA-JP 11 63756016 63756016 single base substitution G A intron_variant BTCA-JP 11 63756101 63756101 single base substitution C T exon_variant BTCA-JP 11 63756101 63756101 single base substitution C T intron_variant BTCA-JP 11 63756101 63756101 single base substitution C T splice_region_variant CESC-US 11 63756108 63756108 single base substitution G C exon_variant CESC-US 11 63756108 63756108 single base substitution G C intron_variant CESC-US 11 63756108 63756108 single base substitution G C missense_variant D44H 130G>C CLLE-ES 11 63755303 63755304 multiple base substitution (>=2bp and <=200bp) GC TT intron_variant CLLE-ES 11 63756811 63756811 single base substitution T C exon_variant CLLE-ES 11 63756811 63756811 single base substitution T C intron_variant CLLE-ES 11 63760034 63760034 single base substitution A G downstream_gene_variant CLLE-ES 11 63760034 63760034 single base substitution A G intron_variant COAD-US 11 63764062 63764062 single base substitution C T exon_variant COAD-US 11 63764062 63764062 single base substitution C T intron_variant COAD-US 11 63764062 63764062 single base substitution C T missense_variant R103W 307C>T COAD-US 11 63764062 63764062 single base substitution C T missense_variant R131W 391C>T COAD-US 11 63764062 63764062 single base substitution C T missense_variant R64W 190C>T COAD-US 11 63764062 63764062 single base substitution C T missense_variant R94W 280C>T COAD-US 11 63764062 63764062 single base substitution C T upstream_gene_variant COAD-US 11 63764526 63764526 single base substitution T C exon_variant COAD-US 11 63764526 63764526 single base substitution T C intron_variant COAD-US 11 63764526 63764526 single base substitution T C missense_variant M113T 338T>C COAD-US 11 63764526 63764526 single base substitution T C missense_variant M143T 428T>C COAD-US 11 63764526 63764526 single base substitution T C missense_variant M152T 455T>C COAD-US 11 63764526 63764526 single base substitution T C missense_variant M180T 539T>C COAD-US 11 63764526 63764526 single base substitution T C missense_variant M42T 125T>C COAD-US 11 63764526 63764526 single base substitution T C upstream_gene_variant COAD-US 11 63764561 63764561 single base substitution G C exon_variant COAD-US 11 63764561 63764561 single base substitution G C missense_variant V125L 373G>C COAD-US 11 63764561 63764561 single base substitution G C missense_variant V155L 463G>C COAD-US 11 63764561 63764561 single base substitution G C missense_variant V164L 490G>C COAD-US 11 63764561 63764561 single base substitution G C missense_variant V192L 574G>C COAD-US 11 63764561 63764561 single base substitution G C missense_variant V54L 160G>C COAD-US 11 63764561 63764561 single base substitution G C upstream_gene_variant COAD-US 11 63764690 63764690 single base substitution C T 3_prime_UTR_variant COAD-US 11 63764690 63764690 single base substitution C T exon_variant COAD-US 11 63764690 63764690 single base substitution C T missense_variant R168W 502C>T COAD-US 11 63764690 63764690 single base substitution C T missense_variant R198W 592C>T COAD-US 11 63764690 63764690 single base substitution C T missense_variant R207W 619C>T COAD-US 11 63764690 63764690 single base substitution C T missense_variant R235W 703C>T COAD-US 11 63764690 63764690 single base substitution C T missense_variant R97W 289C>T COAD-US 11 63764690 63764690 single base substitution C T upstream_gene_variant COAD-US 11 63766861 63766861 single base substitution G A downstream_gene_variant COAD-US 11 63766861 63766861 single base substitution G A intron_variant COAD-US 11 63766861 63766861 single base substitution G A upstream_gene_variant COAD-US 11 63767186 63767186 single base substitution A G downstream_gene_variant COAD-US 11 63767186 63767186 single base substitution A G intron_variant COAD-US 11 63767186 63767186 single base substitution A G upstream_gene_variant COAD-US 11 63767200 63767200 single base substitution C G downstream_gene_variant COAD-US 11 63767200 63767200 single base substitution C G intron_variant COAD-US 11 63767200 63767200 single base substitution C G upstream_gene_variant COCA-CN 11 63752836 63752836 single base substitution C T upstream_gene_variant COCA-CN 11 63758641 63758641 single base substitution T A downstream_gene_variant COCA-CN 11 63758641 63758641 single base substitution T A intron_variant COCA-CN 11 63764901 63764901 single base substitution G A downstream_gene_variant COCA-CN 11 63764901 63764901 single base substitution G A exon_variant COCA-CN 11 63764901 63764901 single base substitution G A splice_region_variant COCA-CN 11 63764901 63764901 single base substitution G A synonymous_variant V132V 396G>A COCA-CN 11 63764901 63764901 single base substitution G A synonymous_variant V203V 609G>A COCA-CN 11 63764901 63764901 single base substitution G A synonymous_variant V233V 699G>A COCA-CN 11 63764901 63764901 single base substitution G A synonymous_variant V242V 726G>A COCA-CN 11 63764901 63764901 single base substitution G A synonymous_variant V270V 810G>A COCA-CN 11 63764901 63764901 single base substitution G A upstream_gene_variant COCA-CN 11 63766415 63766415 single base substitution C A downstream_gene_variant COCA-CN 11 63766415 63766415 single base substitution C A intron_variant COCA-CN 11 63766415 63766415 single base substitution C A upstream_gene_variant ESAD-UK 11 63748558 63748558 single base substitution G C upstream_gene_variant ESAD-UK 11 63748589 63748589 single base substitution G A upstream_gene_variant ESAD-UK 11 63750127 63750127 single base substitution C T upstream_gene_variant ESAD-UK 11 63753944 63753944 single base substitution C A exon_variant ESAD-UK 11 63753944 63753944 single base substitution C A missense_variant P43T 127C>A ESAD-UK 11 63753944 63753944 single base substitution C A missense_variant P6T 16C>A ESAD-UK 11 63753944 63753944 single base substitution C A upstream_gene_variant ESAD-UK 11 63754877 63754877 single base substitution G T intron_variant ESAD-UK 11 63757625 63757625 single base substitution G A exon_variant ESAD-UK 11 63757625 63757625 single base substitution G A intron_variant ESAD-UK 11 63759371 63759371 single base substitution C T downstream_gene_variant ESAD-UK 11 63759371 63759371 single base substitution C T intron_variant ESAD-UK 11 63760211 63760211 single base substitution T C downstream_gene_variant ESAD-UK 11 63760211 63760211 single base substitution T C intron_variant ESAD-UK 11 63763998 63763998 single base substitution G A intron_variant ESAD-UK 11 63763998 63763998 single base substitution G A splice_region_variant ESAD-UK 11 63763998 63763998 single base substitution G A upstream_gene_variant ESAD-UK 11 63766445 63766445 single base substitution G A downstream_gene_variant ESAD-UK 11 63766445 63766445 single base substitution G A intron_variant ESAD-UK 11 63766445 63766445 single base substitution G A upstream_gene_variant ESAD-UK 11 63768485 63768485 single base substitution C G downstream_gene_variant ESAD-UK 11 63768485 63768485 single base substitution C G intron_variant ESAD-UK 11 63768485 63768485 single base substitution C G upstream_gene_variant ESAD-UK 11 63768693 63768693 single base substitution G A downstream_gene_variant ESAD-UK 11 63768693 63768693 single base substitution G A exon_variant ESAD-UK 11 63768693 63768693 single base substitution G A intron_variant ESAD-UK 11 63773075 63773075 single base substitution C T downstream_gene_variant ESCA-CN 11 63767117 63767117 single base substitution C G downstream_gene_variant ESCA-CN 11 63767117 63767117 single base substitution C G intron_variant ESCA-CN 11 63767117 63767117 single base substitution C G upstream_gene_variant ESCA-CN 11 63767128 63767128 single base substitution G A downstream_gene_variant ESCA-CN 11 63767128 63767128 single base substitution G A intron_variant ESCA-CN 11 63767128 63767128 single base substitution G A upstream_gene_variant KIRC-US 11 63764641 63764641 single base substitution C A 3_prime_UTR_variant KIRC-US 11 63764641 63764641 single base substitution C A exon_variant KIRC-US 11 63764641 63764641 single base substitution C A synonymous_variant G151G 453C>A KIRC-US 11 63764641 63764641 single base substitution C A synonymous_variant G181G 543C>A KIRC-US 11 63764641 63764641 single base substitution C A synonymous_variant G190G 570C>A KIRC-US 11 63764641 63764641 single base substitution C A synonymous_variant G218G 654C>A KIRC-US 11 63764641 63764641 single base substitution C A synonymous_variant G80G 240C>A KIRC-US 11 63764641 63764641 single base substitution C A upstream_gene_variant KIRP-US 11 63756155 63756155 single base substitution G T exon_variant KIRP-US 11 63756155 63756155 single base substitution G T intron_variant KIRP-US 11 63756155 63756155 single base substitution G T missense_variant E20D 60G>T KIRP-US 11 63756155 63756155 single base substitution G T missense_variant E50D 150G>T KIRP-US 11 63756155 63756155 single base substitution G T missense_variant E59D 177G>T KIRP-US 11 63756155 63756155 single base substitution G T missense_variant E87D 261G>T LAML-KR 11 63750874 63750874 single base substitution T C upstream_gene_variant LAML-KR 11 63752730 63752730 single base substitution T C upstream_gene_variant LAML-KR 11 63764063 63764063 single base substitution G A exon_variant LAML-KR 11 63764063 63764063 single base substitution G A intron_variant LAML-KR 11 63764063 63764063 single base substitution G A missense_variant R103Q 308G>A LAML-KR 11 63764063 63764063 single base substitution G A missense_variant R131Q 392G>A LAML-KR 11 63764063 63764063 single base substitution G A missense_variant R64Q 191G>A LAML-KR 11 63764063 63764063 single base substitution G A missense_variant R94Q 281G>A LAML-KR 11 63764063 63764063 single base substitution G A upstream_gene_variant LGG-US 11 63764577 63764579 deletion of <=200bp CCT - exon_variant LGG-US 11 63764577 63764579 deletion of <=200bp CCT - inframe_deletion AS130A LGG-US 11 63764577 63764579 deletion of <=200bp CCT - inframe_deletion AS160A LGG-US 11 63764577 63764579 deletion of <=200bp CCT - inframe_deletion AS169A LGG-US 11 63764577 63764579 deletion of <=200bp CCT - inframe_deletion AS197A LGG-US 11 63764577 63764579 deletion of <=200bp CCT - inframe_deletion AS59A LGG-US 11 63764577 63764579 deletion of <=200bp CCT - upstream_gene_variant LICA-FR 11 63765011 63765011 single base substitution A G downstream_gene_variant LICA-FR 11 63765011 63765011 single base substitution A G exon_variant LICA-FR 11 63765011 63765011 single base substitution A G intron_variant LICA-FR 11 63765011 63765011 single base substitution A G missense_variant Y169C 506A>G LICA-FR 11 63765011 63765011 single base substitution A G missense_variant Y240C 719A>G LICA-FR 11 63765011 63765011 single base substitution A G missense_variant Y270C 809A>G LICA-FR 11 63765011 63765011 single base substitution A G missense_variant Y279C 836A>G LICA-FR 11 63765011 63765011 single base substitution A G missense_variant Y307C 920A>G LICA-FR 11 63765011 63765011 single base substitution A G upstream_gene_variant LIHC-US 11 63755856 63755856 single base substitution C A exon_variant LIHC-US 11 63755856 63755856 single base substitution C A synonymous_variant R36R 106C>A LIHC-US 11 63755856 63755856 single base substitution C A synonymous_variant R6R 16C>A LIHC-US 11 63755856 63755856 single base substitution C A synonymous_variant R73R 217C>A LINC-JP 11 63757138 63757138 single base substitution G T exon_variant LINC-JP 11 63757138 63757138 single base substitution G T intron_variant LINC-JP 11 63757139 63757139 single base substitution C T exon_variant LINC-JP 11 63757139 63757139 single base substitution C T intron_variant LINC-JP 11 63766380 63766380 single base substitution G T downstream_gene_variant LINC-JP 11 63766380 63766380 single base substitution G T intron_variant LINC-JP 11 63766380 63766380 single base substitution G T upstream_gene_variant LINC-JP 11 63766839 63766839 single base substitution G A downstream_gene_variant LINC-JP 11 63766839 63766839 single base substitution G A intron_variant LINC-JP 11 63766839 63766839 single base substitution G A upstream_gene_variant LIRI-JP 11 63748356 63748356 single base substitution C A upstream_gene_variant LIRI-JP 11 63748847 63748847 single base substitution G A upstream_gene_variant LIRI-JP 11 63749482 63749482 single base substitution T C upstream_gene_variant LIRI-JP 11 63753410 63753410 single base substitution G A exon_variant LIRI-JP 11 63753410 63753410 single base substitution G A upstream_gene_variant LIRI-JP 11 63757905 63757905 single base substitution C G exon_variant LIRI-JP 11 63757905 63757905 single base substitution C G intron_variant LIRI-JP 11 63758295 63758295 single base substitution A G downstream_gene_variant LIRI-JP 11 63758295 63758295 single base substitution A G intron_variant LIRI-JP 11 63764029 63764029 single base substitution C T exon_variant LIRI-JP 11 63764029 63764029 single base substitution C T intron_variant LIRI-JP 11 63764029 63764029 single base substitution C T missense_variant R120C 358C>T LIRI-JP 11 63764029 63764029 single base substitution C T missense_variant R53C 157C>T LIRI-JP 11 63764029 63764029 single base substitution C T missense_variant R83C 247C>T LIRI-JP 11 63764029 63764029 single base substitution C T missense_variant R92C 274C>T LIRI-JP 11 63764029 63764029 single base substitution C T upstream_gene_variant LIRI-JP 11 63764954 63764954 single base substitution A C downstream_gene_variant LIRI-JP 11 63764954 63764954 single base substitution A C exon_variant LIRI-JP 11 63764954 63764954 single base substitution A C intron_variant LIRI-JP 11 63764954 63764954 single base substitution A C missense_variant E150A 449A>C LIRI-JP 11 63764954 63764954 single base substitution A C missense_variant E221A 662A>C LIRI-JP 11 63764954 63764954 single base substitution A C missense_variant E251A 752A>C LIRI-JP 11 63764954 63764954 single base substitution A C missense_variant E260A 779A>C LIRI-JP 11 63764954 63764954 single base substitution A C missense_variant E288A 863A>C LIRI-JP 11 63764954 63764954 single base substitution A C upstream_gene_variant LIRI-JP 11 63768383 63768383 single base substitution A C downstream_gene_variant LIRI-JP 11 63768383 63768383 single base substitution A C intron_variant LIRI-JP 11 63768383 63768383 single base substitution A C upstream_gene_variant LIRI-JP 11 63769422 63769422 single base substitution A T downstream_gene_variant LIRI-JP 11 63769736 63769736 single base substitution A G downstream_gene_variant LIRI-JP 11 63770860 63770860 single base substitution T G downstream_gene_variant LIRI-JP 11 63771115 63771115 single base substitution A G downstream_gene_variant LIRI-JP 11 63772740 63772740 single base substitution T G downstream_gene_variant LIRI-JP 11 63774099 63774099 single base substitution C T downstream_gene_variant LUSC-KR 11 63751302 63751302 single base substitution C T upstream_gene_variant LUSC-KR 11 63752355 63752355 single base substitution C T upstream_gene_variant LUSC-KR 11 63752416 63752416 single base substitution G A upstream_gene_variant LUSC-KR 11 63753033 63753033 single base substitution T C upstream_gene_variant LUSC-KR 11 63762266 63762266 single base substitution G T downstream_gene_variant LUSC-KR 11 63762266 63762266 single base substitution G T intron_variant LUSC-KR 11 63764827 63764827 single base substitution G C 3_prime_UTR_variant LUSC-KR 11 63764827 63764827 single base substitution G C exon_variant LUSC-KR 11 63764827 63764827 single base substitution G C missense_variant E108Q 322G>C LUSC-KR 11 63764827 63764827 single base substitution G C missense_variant E179Q 535G>C LUSC-KR 11 63764827 63764827 single base substitution G C missense_variant E209Q 625G>C LUSC-KR 11 63764827 63764827 single base substitution G C missense_variant E218Q 652G>C LUSC-KR 11 63764827 63764827 single base substitution G C missense_variant E246Q 736G>C LUSC-KR 11 63764827 63764827 single base substitution G C upstream_gene_variant LUSC-KR 11 63769574 63769574 single base substitution C A downstream_gene_variant LUSC-US 11 63764701 63764701 deletion of <=200bp G - 3_prime_UTR_variant LUSC-US 11 63764701 63764701 deletion of <=200bp G - exon_variant LUSC-US 11 63764701 63764701 deletion of <=200bp G - frameshift_variant K100 LUSC-US 11 63764701 63764701 deletion of <=200bp G - frameshift_variant K171 LUSC-US 11 63764701 63764701 deletion of <=200bp G - frameshift_variant K201 LUSC-US 11 63764701 63764701 deletion of <=200bp G - frameshift_variant K210 LUSC-US 11 63764701 63764701 deletion of <=200bp G - frameshift_variant K238 LUSC-US 11 63764701 63764701 deletion of <=200bp G - upstream_gene_variant LUSC-US 11 63767113 63767113 single base substitution C A downstream_gene_variant LUSC-US 11 63767113 63767113 single base substitution C A intron_variant LUSC-US 11 63767113 63767113 single base substitution C A upstream_gene_variant MALY-DE 11 63748505 63748508 deletion of <=200bp CCTC - upstream_gene_variant MALY-DE 11 63760758 63760759 deletion of <=200bp AG - downstream_gene_variant MALY-DE 11 63760758 63760759 deletion of <=200bp AG - intron_variant MALY-DE 11 63761886 63761886 single base substitution A G downstream_gene_variant MALY-DE 11 63761886 63761886 single base substitution A G intron_variant MALY-DE 11 63771251 63771251 single base substitution C A downstream_gene_variant MALY-DE 11 63773426 63773426 single base substitution G A downstream_gene_variant MELA-AU 11 63748625 63748625 single base substitution C T upstream_gene_variant MELA-AU 11 63749255 63749255 single base substitution C T upstream_gene_variant MELA-AU 11 63750656 63750656 single base substitution C T upstream_gene_variant MELA-AU 11 63750937 63750937 single base substitution G T upstream_gene_variant MELA-AU 11 63751002 63751002 single base substitution C T upstream_gene_variant MELA-AU 11 63751161 63751161 single base substitution C T upstream_gene_variant MELA-AU 11 63752139 63752139 single base substitution C T upstream_gene_variant MELA-AU 11 63752219 63752219 single base substitution C T upstream_gene_variant MELA-AU 11 63752800 63752800 single base substitution A T upstream_gene_variant MELA-AU 11 63752957 63752957 single base substitution C T upstream_gene_variant MELA-AU 11 63753338 63753339 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 11 63753338 63753339 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 63754305 63754305 single base substitution C G intron_variant MELA-AU 11 63754305 63754305 single base substitution C G upstream_gene_variant MELA-AU 11 63754410 63754410 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 63754410 63754410 single base substitution A G intron_variant MELA-AU 11 63754571 63754571 single base substitution C T intron_variant MELA-AU 11 63754883 63754883 single base substitution C T intron_variant MELA-AU 11 63755481 63755481 single base substitution G A intron_variant MELA-AU 11 63755494 63755495 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 63755495 63755495 single base substitution C T intron_variant MELA-AU 11 63756088 63756088 single base substitution C T exon_variant MELA-AU 11 63756088 63756088 single base substitution C T intron_variant MELA-AU 11 63756357 63756357 single base substitution C T exon_variant MELA-AU 11 63756357 63756357 single base substitution C T intron_variant MELA-AU 11 63756573 63756573 single base substitution C A exon_variant MELA-AU 11 63756573 63756573 single base substitution C A intron_variant MELA-AU 11 63757302 63757303 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 11 63757302 63757303 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 63757909 63757909 single base substitution C T exon_variant MELA-AU 11 63757909 63757909 single base substitution C T intron_variant MELA-AU 11 63757952 63757952 single base substitution C T exon_variant MELA-AU 11 63757952 63757952 single base substitution C T intron_variant MELA-AU 11 63757967 63757967 single base substitution G A exon_variant MELA-AU 11 63757967 63757967 single base substitution G A intron_variant MELA-AU 11 63759121 63759121 single base substitution C T downstream_gene_variant MELA-AU 11 63759121 63759121 single base substitution C T intron_variant MELA-AU 11 63759135 63759135 single base substitution G A downstream_gene_variant MELA-AU 11 63759135 63759135 single base substitution G A intron_variant MELA-AU 11 63759487 63759487 single base substitution C T downstream_gene_variant MELA-AU 11 63759487 63759487 single base substitution C T intron_variant MELA-AU 11 63759939 63759939 insertion of <=200bp - GGGGT downstream_gene_variant MELA-AU 11 63759939 63759939 insertion of <=200bp - GGGGT intron_variant MELA-AU 11 63760720 63760720 single base substitution C T downstream_gene_variant MELA-AU 11 63760720 63760720 single base substitution C T intron_variant MELA-AU 11 63762128 63762128 single base substitution G A downstream_gene_variant MELA-AU 11 63762128 63762128 single base substitution G A intron_variant MELA-AU 11 63762255 63762255 single base substitution C T downstream_gene_variant MELA-AU 11 63762255 63762255 single base substitution C T intron_variant MELA-AU 11 63763402 63763402 single base substitution C T intron_variant MELA-AU 11 63763495 63763495 single base substitution G A intron_variant MELA-AU 11 63763768 63763768 single base substitution T A intron_variant MELA-AU 11 63763768 63763768 single base substitution T A upstream_gene_variant MELA-AU 11 63763839 63763839 single base substitution C T intron_variant MELA-AU 11 63763839 63763839 single base substitution C T upstream_gene_variant MELA-AU 11 63764193 63764193 single base substitution C T exon_variant MELA-AU 11 63764193 63764193 single base substitution C T intron_variant MELA-AU 11 63764193 63764193 single base substitution C T upstream_gene_variant MELA-AU 11 63764506 63764506 single base substitution C T intron_variant MELA-AU 11 63764506 63764506 single base substitution C T upstream_gene_variant MELA-AU 11 63764786 63764786 single base substitution C T intron_variant MELA-AU 11 63764786 63764786 single base substitution C T upstream_gene_variant MELA-AU 11 63764892 63764892 single base substitution C T 3_prime_UTR_variant MELA-AU 11 63764892 63764892 single base substitution C T exon_variant MELA-AU 11 63764892 63764892 single base substitution C T synonymous_variant S129S 387C>T MELA-AU 11 63764892 63764892 single base substitution C T synonymous_variant S200S 600C>T MELA-AU 11 63764892 63764892 single base substitution C T synonymous_variant S230S 690C>T MELA-AU 11 63764892 63764892 single base substitution C T synonymous_variant S239S 717C>T MELA-AU 11 63764892 63764892 single base substitution C T synonymous_variant S267S 801C>T MELA-AU 11 63764892 63764892 single base substitution C T upstream_gene_variant MELA-AU 11 63765250 63765250 single base substitution C T 3_prime_UTR_variant MELA-AU 11 63765250 63765250 single base substitution C T downstream_gene_variant MELA-AU 11 63765250 63765250 single base substitution C T exon_variant MELA-AU 11 63765250 63765250 single base substitution C T intron_variant MELA-AU 11 63765250 63765250 single base substitution C T upstream_gene_variant MELA-AU 11 63766232 63766232 single base substitution C T downstream_gene_variant MELA-AU 11 63766232 63766232 single base substitution C T intron_variant MELA-AU 11 63766232 63766232 single base substitution C T upstream_gene_variant MELA-AU 11 63766371 63766371 single base substitution C T downstream_gene_variant MELA-AU 11 63766371 63766371 single base substitution C T intron_variant MELA-AU 11 63766371 63766371 single base substitution C T upstream_gene_variant MELA-AU 11 63766695 63766695 single base substitution G A downstream_gene_variant MELA-AU 11 63766695 63766695 single base substitution G A intron_variant MELA-AU 11 63766695 63766695 single base substitution G A upstream_gene_variant MELA-AU 11 63766723 63766723 single base substitution C T downstream_gene_variant MELA-AU 11 63766723 63766723 single base substitution C T intron_variant MELA-AU 11 63766723 63766723 single base substitution C T upstream_gene_variant MELA-AU 11 63766808 63766808 single base substitution C T downstream_gene_variant MELA-AU 11 63766808 63766808 single base substitution C T intron_variant MELA-AU 11 63766808 63766808 single base substitution C T upstream_gene_variant MELA-AU 11 63767012 63767012 single base substitution G A downstream_gene_variant MELA-AU 11 63767012 63767012 single base substitution G A intron_variant MELA-AU 11 63767012 63767012 single base substitution G A upstream_gene_variant MELA-AU 11 63767340 63767340 single base substitution C T downstream_gene_variant MELA-AU 11 63767340 63767340 single base substitution C T intron_variant MELA-AU 11 63767340 63767340 single base substitution C T upstream_gene_variant MELA-AU 11 63768373 63768373 single base substitution G A downstream_gene_variant MELA-AU 11 63768373 63768373 single base substitution G A intron_variant MELA-AU 11 63768373 63768373 single base substitution G A upstream_gene_variant MELA-AU 11 63770085 63770085 single base substitution C T downstream_gene_variant MELA-AU 11 63771983 63771983 single base substitution G A downstream_gene_variant MELA-AU 11 63772093 63772093 single base substitution C T downstream_gene_variant MELA-AU 11 63772467 63772467 single base substitution G A downstream_gene_variant MELA-AU 11 63773735 63773735 single base substitution G A downstream_gene_variant ORCA-IN 11 63769099 63769099 single base substitution C A downstream_gene_variant ORCA-IN 11 63769099 63769099 single base substitution C A intron_variant OV-AU 11 63753683 63753683 single base substitution T C 5_prime_UTR_variant OV-AU 11 63753683 63753683 single base substitution T C exon_variant OV-AU 11 63753683 63753683 single base substitution T C upstream_gene_variant OV-AU 11 63754771 63754771 single base substitution A G intron_variant OV-AU 11 63766038 63766038 single base substitution C A downstream_gene_variant OV-AU 11 63766038 63766038 single base substitution C A intron_variant OV-AU 11 63766038 63766038 single base substitution C A upstream_gene_variant OV-AU 11 63773669 63773669 single base substitution G T downstream_gene_variant OV-AU 11 63773937 63773937 single base substitution A C downstream_gene_variant PACA-AU 11 63757973 63757973 single base substitution G A exon_variant PACA-AU 11 63757973 63757973 single base substitution G A intron_variant PACA-AU 11 63758062 63758062 insertion of <=200bp - AAAAT downstream_gene_variant PACA-AU 11 63758062 63758062 insertion of <=200bp - AAAAT exon_variant PACA-AU 11 63758062 63758062 insertion of <=200bp - AAAAT intron_variant PACA-AU 11 63758070 63758070 insertion of <=200bp - AAAT downstream_gene_variant PACA-AU 11 63758070 63758070 insertion of <=200bp - AAAT exon_variant PACA-AU 11 63758070 63758070 insertion of <=200bp - AAAT intron_variant PACA-AU 11 63758391 63758391 single base substitution T C downstream_gene_variant PACA-AU 11 63758391 63758391 single base substitution T C intron_variant PACA-AU 11 63761464 63761464 single base substitution C G downstream_gene_variant PACA-AU 11 63761464 63761464 single base substitution C G intron_variant PACA-AU 11 63764204 63764204 single base substitution T G exon_variant PACA-AU 11 63764204 63764204 single base substitution T G intron_variant PACA-AU 11 63764204 63764204 single base substitution T G upstream_gene_variant PACA-AU 11 63765893 63765893 single base substitution C T downstream_gene_variant PACA-AU 11 63765893 63765893 single base substitution C T intron_variant PACA-AU 11 63765893 63765893 single base substitution C T upstream_gene_variant PACA-AU 11 63769729 63769729 single base substitution G A downstream_gene_variant PACA-CA 11 63752324 63752324 single base substitution G C upstream_gene_variant PACA-CA 11 63753455 63753455 single base substitution T A exon_variant PACA-CA 11 63753455 63753455 single base substitution T A upstream_gene_variant PACA-CA 11 63754967 63754967 single base substitution T C intron_variant PACA-CA 11 63757347 63757349 deletion of <=200bp GTG - exon_variant PACA-CA 11 63757347 63757349 deletion of <=200bp GTG - intron_variant PACA-CA 11 63762940 63762940 single base substitution T A downstream_gene_variant PACA-CA 11 63762940 63762940 single base substitution T A intron_variant PACA-CA 11 63766124 63766124 single base substitution C T downstream_gene_variant PACA-CA 11 63766124 63766124 single base substitution C T intron_variant PACA-CA 11 63766124 63766124 single base substitution C T upstream_gene_variant PACA-CA 11 63770852 63770852 single base substitution G T downstream_gene_variant PACA-CA 11 63773651 63773651 single base substitution G C downstream_gene_variant PAEN-AU 11 63772450 63772450 single base substitution G C downstream_gene_variant PBCA-DE 11 63750574 63750574 single base substitution A T upstream_gene_variant PBCA-DE 11 63754019 63754019 single base substitution C T intron_variant PBCA-DE 11 63754019 63754019 single base substitution C T upstream_gene_variant PRAD-CA 11 63762864 63762864 single base substitution C T downstream_gene_variant PRAD-CA 11 63762864 63762864 single base substitution C T intron_variant PRAD-CA 11 63762963 63762963 single base substitution C T downstream_gene_variant PRAD-CA 11 63762963 63762963 single base substitution C T intron_variant PRAD-UK 11 63762119 63762119 single base substitution G C downstream_gene_variant PRAD-UK 11 63762119 63762119 single base substitution G C intron_variant PRAD-UK 11 63764375 63764375 single base substitution G A exon_variant PRAD-UK 11 63764375 63764375 single base substitution G A intron_variant PRAD-UK 11 63764375 63764375 single base substitution G A missense_variant G129S 385G>A PRAD-UK 11 63764375 63764375 single base substitution G A missense_variant G138S 412G>A PRAD-UK 11 63764375 63764375 single base substitution G A missense_variant G166S 496G>A PRAD-UK 11 63764375 63764375 single base substitution G A missense_variant G99S 295G>A PRAD-UK 11 63764375 63764375 single base substitution G A upstream_gene_variant PRAD-US 11 63764357 63764357 single base substitution G T exon_variant PRAD-US 11 63764357 63764357 single base substitution G T intron_variant PRAD-US 11 63764357 63764357 single base substitution G T stop_gained E123* 367G>T PRAD-US 11 63764357 63764357 single base substitution G T stop_gained E132* 394G>T PRAD-US 11 63764357 63764357 single base substitution G T stop_gained E160* 478G>T PRAD-US 11 63764357 63764357 single base substitution G T stop_gained E93* 277G>T PRAD-US 11 63764357 63764357 single base substitution G T upstream_gene_variant READ-US 11 63767186 63767186 single base substitution A G downstream_gene_variant READ-US 11 63767186 63767186 single base substitution A G intron_variant READ-US 11 63767186 63767186 single base substitution A G upstream_gene_variant RECA-EU 11 63761630 63761630 single base substitution T C downstream_gene_variant RECA-EU 11 63761630 63761630 single base substitution T C intron_variant SKCA-BR 11 63748664 63748664 single base substitution G A upstream_gene_variant SKCA-BR 11 63751861 63751861 single base substitution C T upstream_gene_variant SKCA-BR 11 63753613 63753613 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 63753613 63753613 single base substitution G A exon_variant SKCA-BR 11 63753613 63753613 single base substitution G A upstream_gene_variant SKCA-BR 11 63757606 63757606 single base substitution G T exon_variant SKCA-BR 11 63757606 63757606 single base substitution G T intron_variant SKCA-BR 11 63758057 63758057 insertion of <=200bp - TAAAA exon_variant SKCA-BR 11 63758057 63758057 insertion of <=200bp - TAAAA intron_variant SKCA-BR 11 63758069 63758069 insertion of <=200bp - AAAAT downstream_gene_variant SKCA-BR 11 63758069 63758069 insertion of <=200bp - AAAAT exon_variant SKCA-BR 11 63758069 63758069 insertion of <=200bp - AAAAT intron_variant SKCA-BR 11 63761133 63761133 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 11 63761133 63761133 insertion of <=200bp - CA intron_variant SKCA-BR 11 63761504 63761504 single base substitution T G downstream_gene_variant SKCA-BR 11 63761504 63761504 single base substitution T G intron_variant SKCA-BR 11 63761508 63761508 single base substitution A G downstream_gene_variant SKCA-BR 11 63761508 63761508 single base substitution A G intron_variant SKCA-BR 11 63761530 63761530 single base substitution T G downstream_gene_variant SKCA-BR 11 63761530 63761530 single base substitution T G intron_variant SKCA-BR 11 63765691 63765691 single base substitution A C 3_prime_UTR_variant SKCA-BR 11 63765691 63765691 single base substitution A C downstream_gene_variant SKCA-BR 11 63765691 63765691 single base substitution A C exon_variant SKCA-BR 11 63765691 63765691 single base substitution A C intron_variant SKCA-BR 11 63765691 63765691 single base substitution A C upstream_gene_variant SKCA-BR 11 63766375 63766375 single base substitution C T downstream_gene_variant SKCA-BR 11 63766375 63766375 single base substitution C T intron_variant SKCA-BR 11 63766375 63766375 single base substitution C T upstream_gene_variant SKCA-BR 11 63766819 63766819 single base substitution T C downstream_gene_variant SKCA-BR 11 63766819 63766819 single base substitution T C intron_variant SKCA-BR 11 63766819 63766819 single base substitution T C upstream_gene_variant SKCA-BR 11 63767269 63767269 single base substitution T G downstream_gene_variant SKCA-BR 11 63767269 63767269 single base substitution T G intron_variant SKCA-BR 11 63767269 63767269 single base substitution T G upstream_gene_variant SKCA-BR 11 63767966 63767966 single base substitution A C downstream_gene_variant SKCA-BR 11 63767966 63767966 single base substitution A C intron_variant SKCA-BR 11 63767966 63767966 single base substitution A C upstream_gene_variant SKCA-BR 11 63768462 63768462 single base substitution A C downstream_gene_variant SKCA-BR 11 63768462 63768462 single base substitution A C intron_variant SKCA-BR 11 63768462 63768462 single base substitution A C upstream_gene_variant SKCA-BR 11 63768616 63768616 single base substitution G A downstream_gene_variant SKCA-BR 11 63768616 63768616 single base substitution G A exon_variant SKCA-BR 11 63768616 63768616 single base substitution G A intron_variant SKCA-BR 11 63769669 63769669 single base substitution C T downstream_gene_variant SKCA-BR 11 63771593 63771593 single base substitution C A downstream_gene_variant SKCM-US 11 63764603 63764603 single base substitution G A 3_prime_UTR_variant SKCM-US 11 63764603 63764603 single base substitution G A exon_variant SKCM-US 11 63764603 63764603 single base substitution G A missense_variant D139N 415G>A SKCM-US 11 63764603 63764603 single base substitution G A missense_variant D169N 505G>A SKCM-US 11 63764603 63764603 single base substitution G A missense_variant D178N 532G>A SKCM-US 11 63764603 63764603 single base substitution G A missense_variant D206N 616G>A SKCM-US 11 63764603 63764603 single base substitution G A missense_variant D68N 202G>A SKCM-US 11 63764603 63764603 single base substitution G A upstream_gene_variant SKCM-US 11 63764668 63764668 single base substitution C T 3_prime_UTR_variant SKCM-US 11 63764668 63764668 single base substitution C T exon_variant SKCM-US 11 63764668 63764668 single base substitution C T synonymous_variant F160F 480C>T SKCM-US 11 63764668 63764668 single base substitution C T synonymous_variant F190F 570C>T SKCM-US 11 63764668 63764668 single base substitution C T synonymous_variant F199F 597C>T SKCM-US 11 63764668 63764668 single base substitution C T synonymous_variant F227F 681C>T SKCM-US 11 63764668 63764668 single base substitution C T synonymous_variant F89F 267C>T SKCM-US 11 63764668 63764668 single base substitution C T upstream_gene_variant STAD-US 11 63764119 63764119 single base substitution C T exon_variant STAD-US 11 63764119 63764119 single base substitution C T intron_variant STAD-US 11 63764119 63764119 single base substitution C T missense_variant R113W 337C>T STAD-US 11 63764119 63764119 single base substitution C T missense_variant R122W 364C>T STAD-US 11 63764119 63764119 single base substitution C T missense_variant R150W 448C>T STAD-US 11 63764119 63764119 single base substitution C T missense_variant R83W 247C>T STAD-US 11 63764119 63764119 single base substitution C T splice_region_variant STAD-US 11 63764119 63764119 single base substitution C T upstream_gene_variant STAD-US 11 63764564 63764564 single base substitution G A exon_variant STAD-US 11 63764564 63764564 single base substitution G A missense_variant A126T 376G>A STAD-US 11 63764564 63764564 single base substitution G A missense_variant A156T 466G>A STAD-US 11 63764564 63764564 single base substitution G A missense_variant A165T 493G>A STAD-US 11 63764564 63764564 single base substitution G A missense_variant A193T 577G>A STAD-US 11 63764564 63764564 single base substitution G A missense_variant A55T 163G>A STAD-US 11 63764564 63764564 single base substitution G A upstream_gene_variant STAD-US 11 63764867 63764867 single base substitution C T 3_prime_UTR_variant STAD-US 11 63764867 63764867 single base substitution C T exon_variant STAD-US 11 63764867 63764867 single base substitution C T missense_variant A121V 362C>T STAD-US 11 63764867 63764867 single base substitution C T missense_variant A192V 575C>T STAD-US 11 63764867 63764867 single base substitution C T missense_variant A222V 665C>T STAD-US 11 63764867 63764867 single base substitution C T missense_variant A231V 692C>T STAD-US 11 63764867 63764867 single base substitution C T missense_variant A259V 776C>T STAD-US 11 63764867 63764867 single base substitution C T upstream_gene_variant STAD-US 11 63764868 63764868 single base substitution G A 3_prime_UTR_variant STAD-US 11 63764868 63764868 single base substitution G A exon_variant STAD-US 11 63764868 63764868 single base substitution G A synonymous_variant A121A 363G>A STAD-US 11 63764868 63764868 single base substitution G A synonymous_variant A192A 576G>A STAD-US 11 63764868 63764868 single base substitution G A synonymous_variant A222A 666G>A STAD-US 11 63764868 63764868 single base substitution G A synonymous_variant A231A 693G>A STAD-US 11 63764868 63764868 single base substitution G A synonymous_variant A259A 777G>A STAD-US 11 63764868 63764868 single base substitution G A upstream_gene_variant THCA-SA 11 63753848 63753848 deletion of <=200bp G - 5_prime_UTR_variant THCA-SA 11 63753848 63753848 deletion of <=200bp G - exon_variant THCA-SA 11 63753848 63753848 deletion of <=200bp G - frameshift_variant G11 THCA-SA 11 63753848 63753848 deletion of <=200bp G - upstream_gene_variant THCA-US 11 63764532 63764532 single base substitution T C exon_variant THCA-US 11 63764532 63764532 single base substitution T C intron_variant THCA-US 11 63764532 63764532 single base substitution T C missense_variant L115P 344T>C THCA-US 11 63764532 63764532 single base substitution T C missense_variant L145P 434T>C THCA-US 11 63764532 63764532 single base substitution T C missense_variant L154P 461T>C THCA-US 11 63764532 63764532 single base substitution T C missense_variant L182P 545T>C THCA-US 11 63764532 63764532 single base substitution T C missense_variant L44P 131T>C THCA-US 11 63764532 63764532 single base substitution T C upstream_gene_variant UCEC-US 11 63756170 63756170 single base substitution G A exon_variant UCEC-US 11 63756170 63756170 single base substitution G A intron_variant UCEC-US 11 63756170 63756170 single base substitution G A synonymous_variant S25S 75G>A UCEC-US 11 63756170 63756170 single base substitution G A synonymous_variant S55S 165G>A UCEC-US 11 63756170 63756170 single base substitution G A synonymous_variant S64S 192G>A UCEC-US 11 63756170 63756170 single base substitution G A synonymous_variant S92S 276G>A UCEC-US 11 63764119 63764119 single base substitution C T exon_variant UCEC-US 11 63764119 63764119 single base substitution C T intron_variant UCEC-US 11 63764119 63764119 single base substitution C T missense_variant R113W 337C>T UCEC-US 11 63764119 63764119 single base substitution C T missense_variant R122W 364C>T UCEC-US 11 63764119 63764119 single base substitution C T missense_variant R150W 448C>T UCEC-US 11 63764119 63764119 single base substitution C T missense_variant R83W 247C>T UCEC-US 11 63764119 63764119 single base substitution C T splice_region_variant UCEC-US 11 63764119 63764119 single base substitution C T upstream_gene_variant UCEC-US 11 63764651 63764651 single base substitution C T 3_prime_UTR_variant UCEC-US 11 63764651 63764651 single base substitution C T exon_variant UCEC-US 11 63764651 63764651 single base substitution C T missense_variant R155C 463C>T UCEC-US 11 63764651 63764651 single base substitution C T missense_variant R185C 553C>T UCEC-US 11 63764651 63764651 single base substitution C T missense_variant R194C 580C>T UCEC-US 11 63764651 63764651 single base substitution C T missense_variant R222C 664C>T UCEC-US 11 63764651 63764651 single base substitution C T missense_variant R84C 250C>T UCEC-US 11 63764651 63764651 single base substitution C T upstream_gene_variant UCEC-US 11 63764886 63764886 single base substitution C T 3_prime_UTR_variant UCEC-US 11 63764886 63764886 single base substitution C T exon_variant UCEC-US 11 63764886 63764886 single base substitution C T synonymous_variant S127S 381C>T UCEC-US 11 63764886 63764886 single base substitution C T synonymous_variant S198S 594C>T UCEC-US 11 63764886 63764886 single base substitution C T synonymous_variant S228S 684C>T UCEC-US 11 63764886 63764886 single base substitution C T synonymous_variant S237S 711C>T UCEC-US 11 63764886 63764886 single base substitution C T synonymous_variant S265S 795C>T UCEC-US 11 63764886 63764886 single base substitution C T upstream_gene_variant UCEC-US 11 63764926 63764926 single base substitution G A downstream_gene_variant UCEC-US 11 63764926 63764926 single base substitution G A exon_variant UCEC-US 11 63764926 63764926 single base substitution G A intron_variant UCEC-US 11 63764926 63764926 single base substitution G A missense_variant G141S 421G>A UCEC-US 11 63764926 63764926 single base substitution G A missense_variant G212S 634G>A UCEC-US 11 63764926 63764926 single base substitution G A missense_variant G242S 724G>A UCEC-US 11 63764926 63764926 single base substitution G A missense_variant G251S 751G>A UCEC-US 11 63764926 63764926 single base substitution G A missense_variant G279S 835G>A UCEC-US 11 63764926 63764926 single base substitution G A upstream_gene_variant UCEC-US 11 63765247 63765247 single base substitution C T 3_prime_UTR_variant UCEC-US 11 63765247 63765247 single base substitution C T downstream_gene_variant UCEC-US 11 63765247 63765247 single base substitution C T exon_variant UCEC-US 11 63765247 63765247 single base substitution C T splice_region_variant UCEC-US 11 63765247 63765247 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand pfg019T COSM1638913 c.717C>T p.G239G Substitution - coding silent 11:63997447-63997447 + 353T COSM4382933 c.240G>C p.S80S Substitution - coding silent 11:63996550-63996550 + TCGA-AP-A051-01 COSM929978 c.337C>T p.R113W Substitution - Missense 11:63996647-63996647 + ESCC_31 COSM5649682 c.158_159insGCG p.E53_L54insR Insertion - In frame 11:63988691-63988692 + TCGA-B5-A11E-01 COSM929979 c.553C>T p.R185C Substitution - Missense 11:63997179-63997179 + TCGA-CJ-4882-01 COSM467188 c.543C>A p.G181G Substitution - coding silent 11:63997169-63997169 + Gp5D COSM2162879 c.676G>A p.A226T Substitution - Missense 11:63997406-63997406 + TCGA-B5-A11H-01 COSM929977 c.165G>A p.S55S Substitution - coding silent 11:63988698-63988698 + 25 COSM2162865 c.248G>A p.R83H Substitution - Missense 11:63996558-63996558 + CN-AML-NR-22-Dx COSM193918 c.281G>A p.R94Q Substitution - Missense 11:63996591-63996591 + TCGA-HC-7750-01 COSM1470434 c.367G>T p.E123* Substitution - Nonsense 11:63996885-63996885 + DN11153 COSM5962219 c.784C>T p.R262W Substitution - Missense 11:63997514-63997514 + TCGA-DE-A2OL-01 COSM2162869 c.434T>C p.L145P Substitution - Missense 11:63997060-63997060 + HCT116 COSM929979 c.553C>T p.R185C Substitution - Missense 11:63997179-63997179 + TCGA-G4-6628-01 COSM1355602 c.592C>T p.R198W Substitution - Missense 11:63997218-63997218 + 353LT COSM4382933 c.240G>C p.S80S Substitution - coding silent 11:63996550-63996550 + TCGA-AM-5820-01 COSM3687461 c.428T>C p.M143T Substitution - Missense 11:63997054-63997054 + TCGA-BR-8487-01 COSM929978 c.337C>T p.R113W Substitution - Missense 11:63996647-63996647 + TCGA-B5-A0JZ-01 COSM929980 c.684C>T p.S228S Substitution - coding silent 11:63997414-63997414 + TCGA-DI-A0WH-01 COSM929981 c.724G>A p.G242S Substitution - Missense 11:63997454-63997454 + TCGA-HU-A4GQ-01 COSM4035038 c.466G>A p.A156T Substitution - Missense 11:63997092-63997092 + 107519 COSM96097 c.540G>A p.S180S Substitution - coding silent 11:63997166-63997166 + TCGA-D9-A3Z1-06 COSM3451356 c.570C>T p.F190F Substitution - coding silent 11:63997196-63997196 + CSCC-45-T COSM4498070 c.511C>T p.L171F Substitution - Missense 11:63997137-63997137 + CHC1747T COSM4788102 c.809A>G p.Y270C Substitution - Missense 11:63997539-63997539 + TCGA-AY-6197-01 COSM1355601 c.463G>C p.V155L Substitution - Missense 11:63997089-63997089 + TCGA-BR-7851-01 COSM4035042 c.666G>A p.A222A Substitution - coding silent 11:63997396-63997396 + LUAD-NYU847 COSM376584 c.778C>T p.L260F Substitution - Missense 11:63997508-63997508 + XHDG09 COSM4768547 c.6G>A p.A2A Substitution - coding silent 11:63986462-63986462 + TCGA-B9-4115-01 COSM3986327 c.150G>T p.E50D Substitution - Missense 11:63988683-63988683 + Pat_16_B COSM5839124 c.593G>A p.R198Q Substitution - Missense 11:63997219-63997219 + Gp2D COSM2162879 c.676G>A p.A226T Substitution - Missense 11:63997406-63997406 + CHC1747T COSM4788102 c.809A>G p.Y270C Substitution - Missense 11:63997539-63997539 + CN-AML-22-T COSM193918 c.281G>A p.R94Q Substitution - Missense 11:63996591-63996591 + RK241_C01 COSM4778594 c.752A>C p.E251A Substitution - Missense 11:63997482-63997482 + ccRCC-44 COSM1663296 c.808T>C p.Y270H Substitution - Missense 11:63997538-63997538 + RK189_C01 COSM1628144 c.247C>T p.R83C Substitution - Missense 11:63996557-63996557 + STC291 COSM5050987 c.554G>A p.R185H Substitution - Missense 11:63997180-63997180 + HCT-116 COSM929979 c.553C>T p.R185C Substitution - Missense 11:63997179-63997179 + TCGA-D5-6927-01 COSM1355600 c.280C>T p.R94W Substitution - Missense 11:63996590-63996590 + HCT116 COSM2162878 c.672C>A p.A224A Substitution - coding silent 11:63997402-63997402 + TCGA-EE-A29G-06 COSM3451354 c.505G>A p.D169N Substitution - Missense 11:63997131-63997131 + TCGA-FP-A4BE-01 COSM4035040 c.665C>T p.A222V Substitution - Missense 11:63997395-63997395 + LP6005690-DNA_D01 COSM2162863 c.220-4G>A p.? Unknown 11:63996526-63996526 + SNU-C4 COSM4652001 c.240G>A p.S80S Substitution - coding silent 11:63996550-63996550 + YUKAT COSM5373181 c.659T>C p.I220T Substitution - Missense 11:63997389-63997389 + TCGA-DD-A4NQ-01 COSM4941090 c.106C>A p.R36R Substitution - coding silent 11:63988384-63988384 + TCGA-D8-A27L-01 COSM1475697 c.404T>C p.I135T Substitution - Missense 11:63996922-63996922 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.473761;Hs.473788 11q13.1 608337

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - C 3-UTRInsertion . c.813+129dupC 11 63765136 CM C A Synonymous p.G181G c.543C>A 11 63764641 RCCC CCT - InFrameDeletion p.S161delS c.482_484delCCT 11 63764577 LGG C T Synonymous p.G239G c.717C>T 11 63764919 STAD C T Synonymous p.S228S c.684C>T 11 63764886 UCEC G A Missense p.D107N c.319G>A 11 63764101 HNSC G A Missense p.D169N c.505G>A 11 63764603 CM G A Missense p.G242S c.724G>A 11 63764926 UCEC G A Synonymous p.E186E c.558G>A 11 63764656 CM G A Synonymous p.S55S c.165G>A 11 63756170 UCEC G - Frameshift p.E202Sfs*185 c.604delG 11 63764701 LUSC G T Nonsense p.E123* c.367G>T 11 63764357 PRAD T C Missense p.I135T c.404T>C 11 63764394 BRCA T C Missense p.L145P c.434T>C 11 63764532 THCA