L17F (p.Leu17Phe) variant of FGG (Fibrinogen gamma chain)
L17F (p.Leu17Phe) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
L17F (p.Leu17Phe) variant details
- p.Leu17Phe
- ExAC rs760142840
- TOPMed rs760142840
- gnomAD rs760142840
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.02
- CADD 16.10
- Most common in the HGDP:ADYGEI population (allele frequency 0.029)
- Structural context available