1. Directory
  2. Sequencing
  3. Whole-genome resequencing
  4. Variant annotation
Join community Sign in

A database and a web interface that is designed to fill the annotation gap left by the high cost of experimental testing for functional significance of protein variants.

Restrictions to use:
View all reviews

0 user review

No review has been posted.

View all issues

0 issue

No open issue.

  • (Schaefer et al., 2012) SNPdbe: constructing an nsSNP functional impacts database. Bioinformatics.
    PMID: 22210871
  • Animals
    • Homo sapiens

61 related tools