E152D (p.Glu152Asp) variant of FGG (Fibrinogen gamma chain)
E152D (p.Glu152Asp) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
E152D (p.Glu152Asp) variant details
- p.Glu152Asp
- ExAC rs757252622
- TOPMed rs757252622
- gnomAD rs757252622
- Missense
- Variant Prioritization Score for Impact Estimate 0.162
- REVEL 0.04
- CADD 14.40
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available