G71E (p.Gly71Glu) variant of LHCGR (P22888)
G71E (p.Gly71Glu) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
G71E (p.Gly71Glu) variant details
- p.Gly71Glu
- TOPMed rs1668971448
- gnomAD rs1668971448
- Missense
- Variant Prioritization Score for Impact Estimate 0.662
- REVEL 0.65
- CADD 24.10
- PolyPhen-2 1.00
- SIFT 0.24
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available