Current Release: dbNSFP v5.1 (March 21, 2025) (Highlights, README v5.1a, README v5.1c, Change Log)
Rebuilt variant set (all potential nsSNVs and ssSNVs) based on latest GENCODE release 47 (Ensembl v113).
Added Allele frequencies from All of Us (250k genomes) and Regeneron Genetics Center Million Exome (RGC-ME) (Thanks to Moez Dawood and Dr. Richard Gibbs from HGSC at Baylor College of Medicine).
Please note RGC-ME allele frequency data is only available in v5.1a for academia use only.
Added dbNSFP_POPMAX_AF/AC etc. based on all population allele frequency columns curated in dbNSFP.
Updated MutationTaster2021 to include more missense mutations (Thanks to Franziska Fritz and Dr. Dominik Seelow from Berlin Institute of Health).
Other updated resources include Clinvar, GWAS catalog, OMIM, Orphanet, ClinGen Dosage Sensitivity, Interpro, HGNC, Uniprot, IntAct, Gene Ontology, MGI, ZFIN, UniParc, RefSeq, MANE, and HPO.
Provided dbNSFP files in a format ready to use with Ensembl Variant Effect Predictor (VEP) (Thanks to Dr. Jamie Allen from EMBL-EBI) and SnpSift.