G29D (p.Gly29Asp) variant of NPR1 (P16066)
G29D (p.Gly29Asp) 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 and structural context.
G29D (p.Gly29Asp) variant details
- p.Gly29Asp
- 1000Genomes rs1215380888
- TOPMed rs1215380888
- gnomAD rs1215380888
- Missense
- Variant Prioritization Score for Impact Estimate 0.244
- REVEL 0.20
- CADD 9.76
- PolyPhen-2 0.00
- SIFT 0.56
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available