NCBI. The Blood Group Antigen Gene Mutation Database (dbRBC) documents variations in genes that directly or indirectly affect blood groups. It thus is a locus-specific mutation database (LSDB) that covers multiple genes.
Search for information on defects in the Bruton tyrosine kinase (BTK) gene, which causes agammaglobulinemia (XLA). USE WITH CAUTION: DATABASE HAS NOT BEEN UPDATED SINCE 2008.
The Genome Variation Server (GVS) is a local database hosted by the SeattleSNPs Program for Genomic Applications (PGA). The objective of this database is to provide a simple tool for rapid access to human genotype data found in dbSNP, and to provide tools for analysis of genotype data.
The HGVS' list of variation databases includes SNP and locus specific databases. Users are encouraged to check the currency of databases when using them.
The goal of MutDB is to annotate human variation data with protein structural information and other functionally relevant information, if available. The mutations are organized by gene.