E32G (p.Glu32Gly) variant of LHCGR (P22888)
E32G (p.Glu32Gly) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
E32G (p.Glu32Gly) variant details
- p.Glu32Gly
- Ensembl rs2103767289
- Missense
- Variant Prioritization Score for Impact Estimate 0.337
- REVEL 0.32
- CADD 23.20
- PolyPhen-2 0.04
- SIFT 0.30
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available