Q9P (p.Gln9Pro) variant of LHCGR (P22888)
Q9P (p.Gln9Pro) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
Q9P (p.Gln9Pro) variant details
- p.Gln9Pro
- TOPMed rs1217411859
- gnomAD rs1217411859
- Missense
- Variant Prioritization Score for Impact Estimate 0.096
- REVEL 0.12
- CADD 1.59
- PolyPhen-2 0.00
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available