W11G (p.Trp11Gly) variant of LEP (Leptin)
W11G (p.Trp11Gly) in LEP (Leptin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data, published literature, and structural context.
W11G (p.Trp11Gly) variant details
- p.Trp11Gly
- gnomAD 7-128252049-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.372
- REVEL 0.43
- CADD 22.00
- PolyPhen-2 0.00
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available