N69D (p.Asn69Asp) variant of PICALM (Q13492)
N69D (p.Asn69Asp) in PICALM (Q13492) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
N69D (p.Asn69Asp) variant details
- p.Asn69Asp
- Ensembl rs1565480624
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- REVEL 0.25
- CADD 24.30
- PolyPhen-2 0.14
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available