G38E (p.Gly38Glu) variant of PGR (Progesterone receptor)
G38E (p.Gly38Glu) in PGR (Progesterone receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
G38E (p.Gly38Glu) variant details
- p.Gly38Glu
- 1000Genomes rs547307017
- ExAC rs547307017
- TOPMed rs547307017
- gnomAD rs547307017
- Missense
- Variant Prioritization Score for Impact Estimate 0.0606
- REVEL 0.04
- CADD 4.08
- PolyPhen-2 0.00
- SIFT 0.26
- Most common in the 1KG:PJL population (allele frequency 0.0052)
- Structural context available