G68R (p.Gly68Arg) variant of FSHR (P23945)
G68R (p.Gly68Arg) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data and structural context.
G68R (p.Gly68Arg) variant details
- p.Gly68Arg
- TOPMed rs1669585703
- Missense
- Variant Prioritization Score for Impact Estimate 0.724
- REVEL 0.73
- MetaLR 0.85
- MetaSVM 0.79
- CADD 23.80
- PolyPhen-2 0.43
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available