A68D (p.Ala68Asp) variant of LHCGR (P22888)
A68D (p.Ala68Asp) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data and structural context.
A68D (p.Ala68Asp) variant details
- p.Ala68Asp
- TOPMed rs944199288
- gnomAD rs944199288
- Missense
- Variant Prioritization Score for Impact Estimate 0.799
- REVEL 0.81
- CADD 26.10
- PolyPhen-2 1.00
- SIFT 0.00
- Population evidence available
- Structural context available