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Human Genome build 36.3, dbSNP build 129

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What is SNP500Cancer? WHAT'S NEW with SNP500Cancer?

The goal of the SNP500Cancer project is to resequence 102 reference samples to find known or newly discovered single nucleotide polymorphisms (SNPs) which are of immediate importance to molecular epidemiology studies in cancer. SNP500Cancer provides a central resource for sequence verification of SNPs. For more information, see SNP500Cancer background.

Search for SNPs in SNP500Cancer database

You can search for SNPs using SNP identifier, gene symbol, gene alias, chromosome location,
or gene ontology pathway.
  • by SNP identifier
    to display SNP details, allele and genotype frequencies
Enter the dbSNP ID or internal SNP ID: search hints
  • by Gene
    to display SNPs on the gene, and haplotype data
Enter gene symbol, alias, or GenBank ID: search hints
    or:   List genes with analyzed SNPs
    or:   List genes with pending SNPs
Enter chromosome number: search hints
Enter GO Pathway (text or numeric): search hints



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