P18Q (p.Pro18Gln) variant of PGR (Progesterone receptor)
P18Q (p.Pro18Gln) in PGR (Progesterone receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
P18Q (p.Pro18Gln) variant details
- p.Pro18Gln
- ExAC rs759568940
- TOPMed rs759568940
- gnomAD rs759568940
- Missense
- Variant Prioritization Score for Impact Estimate 0.178
- REVEL 0.06
- CADD 20.20
- PolyPhen-2 0.25
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available