A91T (p.Ala91Thr) variant of LHCGR (P22888)
A91T (p.Ala91Thr) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
A91T (p.Ala91Thr) variant details
- p.Ala91Thr
- TOPMed rs1460068431
- gnomAD rs1460068431
- Missense
- Variant Prioritization Score for Impact Estimate 0.518
- REVEL 0.35
- CADD 24.60
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available