W99G (p.Trp99Gly) variant of NOS1AP (O75052)
W99G (p.Trp99Gly) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
W99G (p.Trp99Gly) variant details
- p.Trp99Gly
- TOPMed rs1028428519
- Missense
- Variant Prioritization Score for Impact Estimate 0.483
- REVEL 0.40
- CADD 25.50
- PolyPhen-2 0.07
- SIFT 0.02
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available