D95G (p.Asp95Gly) variant of LHCGR (P22888)
D95G (p.Asp95Gly) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
D95G (p.Asp95Gly) variant details
- p.Asp95Gly
- gnomAD rs1450652801
- Missense
- Variant Prioritization Score for Impact Estimate 0.619
- REVEL 0.61
- CADD 23.70
- PolyPhen-2 0.62
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available