V37A (p.Val37Ala) variant of NOS1AP (O75052)
V37A (p.Val37Ala) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
V37A (p.Val37Ala) variant details
- p.Val37Ala
- TOPMed rs1259606971
- gnomAD rs1259606971
- Missense
- Variant Prioritization Score for Impact Estimate 0.378
- REVEL 0.22
- CADD 24.10
- PolyPhen-2 0.31
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available