L86L (p.Leu86Leu) variant of LEP (Leptin)
L86L (p.Leu86Leu) in LEP (Leptin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
L86L (p.Leu86Leu) variant details
- p.Leu86Leu
- rs772575402
- gnomAD 7-128254517-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.272
- CADD 4.06
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available