F9L (p.Phe9Leu) variant of LEP (Leptin)
F9L (p.Phe9Leu) in LEP (Leptin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
F9L (p.Phe9Leu) variant details
- p.Phe9Leu
- rs1401846669
- NCI-TCGA Cosmic COSV5824
- TOPMed rs1401846669
- gnomAD rs1401846669
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.25
- REVEL 0.04
- CADD 4.94
- PolyPhen-2 0.01
- SIFT 0.62
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available