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 8 7833944 7833944 single base substitution T A exon_variant BLCA-CN 8 7834120 7834120 single base substitution G A exon_variant BLCA-CN 8 7834257 7834257 single base substitution T G exon_variant BLCA-CN 8 7834885 7834885 single base substitution A T exon_variant BLCA-CN 8 7835487 7835487 single base substitution G C exon_variant BRCA-EU 8 7834188 7834188 single base substitution G C exon_variant LAML-KR 8 7830046 7830046 single base substitution C T downstream_gene_variant LAML-KR 8 7830581 7830581 single base substitution C A downstream_gene_variant LAML-KR 8 7830596 7830596 single base substitution T C downstream_gene_variant LAML-KR 8 7830642 7830642 single base substitution G C downstream_gene_variant LAML-KR 8 7830701 7830701 single base substitution T G downstream_gene_variant LAML-KR 8 7830807 7830807 single base substitution T G downstream_gene_variant LAML-KR 8 7830828 7830828 single base substitution C A downstream_gene_variant LAML-KR 8 7834512 7834512 single base substitution G A exon_variant LAML-KR 8 7835287 7835287 single base substitution C G exon_variant LIAD-FR 8 7834872 7834872 single base substitution C G exon_variant LIAD-FR 8 7834959 7834959 single base substitution T C exon_variant LUSC-KR 8 7830297 7830297 single base substitution T C downstream_gene_variant LUSC-KR 8 7834649 7834649 single base substitution C T exon_variant LUSC-KR 8 7834671 7834671 single base substitution G T exon_variant LUSC-KR 8 7834677 7834677 single base substitution G A exon_variant LUSC-KR 8 7835203 7835203 single base substitution A G exon_variant LUSC-KR 8 7835259 7835259 single base substitution C G exon_variant LUSC-KR 8 7835287 7835287 single base substitution C G exon_variant MELA-AU 8 7838839 7838839 single base substitution C T upstream_gene_variant MELA-AU 8 7840158 7840158 single base substitution G A upstream_gene_variant

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.741131 8p23.1