S112F (p.Ser112Phe) variant of FGG (Fibrinogen gamma chain)
S112F (p.Ser112Phe) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
S112F (p.Ser112Phe) variant details
- p.Ser112Phe
- TOPMed rs1221237667
- Missense
- Variant Prioritization Score for Impact Estimate 0.503
- REVEL 0.57
- CADD 22.10
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available