Y87N (p.Tyr87Asn) variant of PGR (Progesterone receptor)
Y87N (p.Tyr87Asn) in PGR (Progesterone receptor) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. 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.
Y87N (p.Tyr87Asn) variant details
- p.Tyr87Asn
- rs751679548
- ClinGen CA382486294
- ClinVar RCV004498767
- ExAC rs751679548
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.158
- REVEL 0.04
- CADD 18.60
- PolyPhen-2 0.13
- SIFT 0.03
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available