G98D (p.Gly98Asp) variant of PGR (Progesterone receptor)
G98D (p.Gly98Asp) in PGR (Progesterone receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
G98D (p.Gly98Asp) variant details
- p.Gly98Asp
- Ensembl rs1862990021
- Missense
- Variant Prioritization Score for Impact Estimate 0.101
- REVEL 0.02
- CADD 11.00
- PolyPhen-2 0.01
- SIFT 0.06
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available