P2S (p.Pro2Ser) variant of NOS1AP (O75052)
P2S (p.Pro2Ser) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
P2S (p.Pro2Ser) variant details
- p.Pro2Ser
- TOPMed rs1691631077
- gnomAD rs1691631077
- Missense
- Variant Prioritization Score for Impact Estimate 0.519
- REVEL 0.42
- CADD 25.20
- PolyPhen-2 0.51
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available