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DBASS3 and DBASS5 is a database of new exon boundaries induced by pathogenic mutations in human disease genes. DBASS3 is a publicly accessible resource containing details of aberrant splice sites generated as a result in disease-causing mutations in human genes. Nucleotide sequences of authentic and aberrant splice acceptor sites can be retrieved by phenotype, gene, mutation, by the location of cryptic/de novo acceptor sites, and by their distance from authentic sites. DBASS3 also provides a basic summary of cryptic and de novo splice sites and their distribution across exons and introns.


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