A38D (p.Ala38Asp) variant of NPR1 (P16066)
A38D (p.Ala38Asp) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
A38D (p.Ala38Asp) variant details
- p.Ala38Asp
- gnomAD 1-153679221-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.683
- REVEL 0.65
- CADD 24.80
- PolyPhen-2 0.98
- SIFT 0.02
- Population evidence available
- Structural context available
- Literature evidence available