G65G (p.Gly65Gly) variant of LEP (Leptin)
G65G (p.Gly65Gly) in LEP (Leptin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
G65G (p.Gly65Gly) variant details
- p.Gly65Gly
- rs761690570
- gnomAD 7-128254454-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0862
- CADD 0.78
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available