S39G (p.Ser39Gly) variant of NOS1AP (O75052)
S39G (p.Ser39Gly) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
S39G (p.Ser39Gly) variant details
- p.Ser39Gly
- gnomAD 1-162154414-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.359
- REVEL 0.21
- MetaLR 0.08
- MetaSVM -0.96
- CADD 26.20
- PolyPhen-2 0.64
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available