N22K (p.Asn22Lys) variant of NOS1AP (O75052)
N22K (p.Asn22Lys) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
N22K (p.Asn22Lys) variant details
- p.Asn22Lys
- TOPMed rs1485371363
- gnomAD rs1485371363
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.14
- CADD 26.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available