V39M (p.Val39Met) variant of NPR1 (P16066)
V39M (p.Val39Met) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
V39M (p.Val39Met) variant details
- p.Val39Met
- gnomAD 1-153679223-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.552
- REVEL 0.42
- CADD 25.40
- PolyPhen-2 0.93
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available