P7S (p.Pro7Ser) variant of NPR1 (P16066)
P7S (p.Pro7Ser) 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.
P7S (p.Pro7Ser) variant details
- p.Pro7Ser
- TOPMed rs1052318333
- gnomAD rs1052318333
- Missense
- Variant Prioritization Score for Impact Estimate 0.247
- REVEL 0.21
- CADD 14.10
- PolyPhen-2 0.00
- SIFT 0.34
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available