Q82R (p.Gln82Arg) variant of LHCGR (P22888)
Q82R (p.Gln82Arg) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data and structural context.
Q82R (p.Gln82Arg) variant details
- p.Gln82Arg
- ExAC rs766156571
- gnomAD rs766156571
- Missense
- Variant Prioritization Score for Impact Estimate 0.647
- REVEL 0.66
- CADD 23.90
- PolyPhen-2 0.99
- SIFT 0.12
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available