R13H (p.Arg13His) variant of NPR1 (P16066)
R13H (p.Arg13His) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
R13H (p.Arg13His) variant details
- p.Arg13His
- gnomAD 1-153679146-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.241
- REVEL 0.29
- CADD 15.10
- PolyPhen-2 0.17
- SIFT 0.19
- Population evidence available
- Structural context available
- Literature evidence available