F9F (p.Phe9Phe) variant of LEP (Leptin)
F9F (p.Phe9Phe) in LEP (Leptin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data, published literature, and structural context.
F9F (p.Phe9Phe) variant details
- p.Phe9Phe
- gnomAD 7-128252045-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.526
- CADD 2.79
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available