D39E (p.Asp39Glu) variant of LHCGR (P22888)
D39E (p.Asp39Glu) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
D39E (p.Asp39Glu) variant details
- p.Asp39Glu
- gnomAD rs1472140371
- Missense
- Variant Prioritization Score for Impact Estimate 0.131
- REVEL 0.10
- CADD 14.00
- PolyPhen-2 0.04
- SIFT 0.55
- Population evidence available
- Structural context available