SeattleSeq Annotation 137

SeattleSeq Annotation

The SeattleSeq Annotation server provides annotation of SNVs (single-nucleotide variations) and indels, both known and novel. This annotation includes dbSNP rs ID, gene names and accession numbers, variation functions (e.g. missense), protein positions and amino-acid changes, conservation scores, HapMap frequencies, PolyPhen predictions, and clinical association. Links to other annotation sites are also provided.

Data from a number of sources has been pooled to create a local database from which many of the properties are drawn. This is the same database that is used by the Genome Variation Server (GVS).

This site is supported by the National Heart, Lung and Blood Institute (NHLBI).

Please see the terms of service.

The site is briefly described in this publication: Nature 2009 Sep 10;461(7261):272-6, Targeted capture and massively parallel sequencing of 12 human exomes, S. B. Ng et al.
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