G33D (p.Gly33Asp) variant of NPR1 (P16066)
G33D (p.Gly33Asp) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
G33D (p.Gly33Asp) variant details
- p.Gly33Asp
- TOPMed rs1669686966
- Missense
- Variant Prioritization Score for Impact Estimate 0.163
- REVEL 0.08
- CADD 9.35
- PolyPhen-2 0.05
- SIFT 0.55
- Population evidence available
- Structural context available