synonymous variant associated_with SNV

Subject: synonymous variant
Relation: associated_with
Object: SNV
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012) PMID:22604720 cited

47% of all SNVs (74% of nonsynonymous and 6% of synonymous variants) are predicted to be deleterious

confidence: 0.95