What is dbNSFP? 

dbNSFP is a comprehensive, one-stop resource for functional annotations and deleteriousness predictions of all possible non-synonymous single-nucleotide variants (nsSNVs) in the human genome. Since its initial release in 2011, dbNSFP has established itself as a trusted data infrastructure advancing human genetic and clinical genomic research (Publications) and powering regulatory-compliant clinical genomics platforms worldwide.

Its current version is based on GENCODE Human release 48 (Ensembl version 114) and includes a total of 81.5M nsSNVs and 2.2M ssSNVs (splicing-site SNVs) derived from all known protein-coding genes in the human genome (includes mitochondrial DNA).

dbNSFP compiles functional annotations and deleteriousness prediction scores from 34 algorithms: 

Evolutionary conservation scores:

and observed allele frequencies from large population sequencing projects:

Moreover, dbNSFP curates comprehensive gene-level annotations, including:

For a full list of data sources and version information, please refer to the current README of dbNSFP in the Releases page.

Developer Collaboration

We welcome developers of functional prediction methods to provide their predictions and scores to the database. Please contact us at collaboration@dbnsfp.org.