P18R (p.Pro18Arg) variant of PGR (Progesterone receptor)
P18R (p.Pro18Arg) in PGR (Progesterone receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P18R (p.Pro18Arg) variant details
- p.Pro18Arg
- ExAC rs759568940
- TOPMed rs759568940
- gnomAD rs759568940
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.03
- CADD 20.30
- PolyPhen-2 0.25
- SIFT 0.03
- Most common in the East Asian population (allele frequency 2.6e-05)
- Structural context available