G29V (p.Gly29Val) variant of NPR1 (P16066)
G29V (p.Gly29Val) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
G29V (p.Gly29Val) variant details
- p.Gly29Val
- gnomAD 1-153679194-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.249
- REVEL 0.20
- CADD 11.70
- PolyPhen-2 0.00
- SIFT 0.26
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available