P21R (p.Pro21Arg) variant of NPR1 (P16066)
P21R (p.Pro21Arg) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
P21R (p.Pro21Arg) variant details
- p.Pro21Arg
- gnomAD 1-153679170-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.197
- REVEL 0.21
- CADD 10.90
- PolyPhen-2 0.01
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available
- Literature evidence available