G29S (p.Gly29Ser) variant of NPR1 (P16066)
G29S (p.Gly29Ser) 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 and structural context.
G29S (p.Gly29Ser) variant details
- p.Gly29Ser
- Ensembl rs1571343280
- Missense
- Variant Prioritization Score for Impact Estimate 0.25
- REVEL 0.18
- CADD 13.40
- PolyPhen-2 0.00
- SIFT 0.75
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available