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Article

dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations.

Human mutation - 1 Sept 2013

Liu Xiaoming, Jian Xueqiu, Boerwinkle Eric

Abstract excerpt

dbNSFP is a database developed for functional prediction and annotation of all potential non-synonymous single-nucleotide variants (nsSNVs) in the human genome. This database significantly facilitates the process of querying predictions and annotations from different databases/web-servers for large amounts of nsSNVs discovered in exome-sequencing studies. Here we report a recent major update of the database to...

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Identifiers

PMID: 23843252
DOI: 10.1002/humu.22376
PMCID: PMC4109890

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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