D95V (p.Asp95Val) variant of LHCGR (P22888)
D95V (p.Asp95Val) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
D95V (p.Asp95Val) variant details
- p.Asp95Val
- gnomAD rs1450652801
- Missense
- Variant Prioritization Score for Impact Estimate 0.612
- REVEL 0.60
- CADD 23.70
- PolyPhen-2 0.88
- SIFT 0.48
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available