D76G (p.Asp76Gly) variant of LEP (Leptin)
D76G (p.Asp76Gly) in LEP (Leptin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
D76G (p.Asp76Gly) variant details
- p.Asp76Gly
- gnomAD rs1332916395
- Missense
- Variant Prioritization Score for Impact Estimate 0.595
- REVEL 0.69
- CADD 23.90
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available