E115D (p.Glu115Asp) variant of LHCGR (P22888)
E115D (p.Glu115Asp) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
E115D (p.Glu115Asp) variant details
- p.Glu115Asp
- gnomAD rs1668688977
- Missense
- Variant Prioritization Score for Impact Estimate 0.263
- REVEL 0.27
- CADD 15.20
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available