N69N (p.Asn69Asn) variant of DAP3 (P51398)
N69N (p.Asn69Asn) in DAP3 (P51398) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data, published literature, and structural context.
N69N (p.Asn69Asn) variant details
- p.Asn69Asn
- gnomAD 1-155721555-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.466
- CADD 14.30
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available