G117R (p.Gly117Arg) variant of LHCGR (P22888)
G117R (p.Gly117Arg) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
G117R (p.Gly117Arg) variant details
- p.Gly117Arg
- cosmic curated COSV99683
- TOPMed rs1209521626
- gnomAD rs1209521626
- Missense
- Variant Prioritization Score for Impact Estimate 0.675
- REVEL 0.69
- CADD 23.50
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available