A28G (p.Ala28Gly) variant of LHCGR (P22888)
A28G (p.Ala28Gly) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
A28G (p.Ala28Gly) variant details
- p.Ala28Gly
- TOPMed rs1352747382
- gnomAD rs1352747382
- Missense
- Variant Prioritization Score for Impact Estimate 0.206
- REVEL 0.14
- CADD 16.80
- PolyPhen-2 0.02
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 8.4e-06)
- Structural context available