N69S (p.Asn69Ser) variant of PICALM (Q13492)
N69S (p.Asn69Ser) in PICALM (Q13492) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
N69S (p.Asn69Ser) variant details
- p.Asn69Ser
- TOPMed rs1355269529
- Missense
- Variant Prioritization Score for Impact Estimate 0.326
- REVEL 0.13
- CADD 22.30
- PolyPhen-2 0.01
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available