L59V (p.Leu59Val) variant of LHCGR (P22888)
L59V (p.Leu59Val) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
L59V (p.Leu59Val) variant details
- p.Leu59Val
- gnomAD rs1668973210
- Missense
- Variant Prioritization Score for Impact Estimate 0.694
- REVEL 0.71
- CADD 25.50
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available