P69S (p.Pro69Ser) variant of PGR (Progesterone receptor)
P69S (p.Pro69Ser) in PGR (Progesterone receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data and structural context.
P69S (p.Pro69Ser) variant details
- p.Pro69Ser
- ExAC rs776395620
- TOPMed rs776395620
- gnomAD rs776395620
- Missense
- Variant Prioritization Score for Impact Estimate 0.0273
- REVEL 0.01
- CADD 0.43
- PolyPhen-2 0.00
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 1.3e-05)
- Structural context available