D41V (p.Asp41Val) variant of NOS1AP (O75052)
D41V (p.Asp41Val) 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.
D41V (p.Asp41Val) variant details
- p.Asp41Val
- gnomAD rs1207434900
- Missense
- Variant Prioritization Score for Impact Estimate 0.519
- REVEL 0.41
- CADD 30.00
- PolyPhen-2 0.99
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available