Q9L (p.Gln9Leu) variant of LHCGR (P22888)
Q9L (p.Gln9Leu) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
Q9L (p.Gln9Leu) variant details
- p.Gln9Leu
- TOPMed rs1217411859
- gnomAD rs1217411859
- Missense
- Variant Prioritization Score for Impact Estimate 0.0862
- REVEL 0.10
- CADD 2.26
- PolyPhen-2 0.00
- SIFT 0.05
- Population evidence available
- Structural context available