Q67E (p.Gln67Glu) variant of LHCGR (P22888)
Q67E (p.Gln67Glu) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
Q67E (p.Gln67Glu) variant details
- p.Gln67Glu
- ExAC rs780523667
- gnomAD rs780523667
- Missense
- Variant Prioritization Score for Impact Estimate 0.485
- REVEL 0.36
- CADD 23.00
- PolyPhen-2 0.53
- SIFT 0.39
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available