Q91H (p.Gln91His) variant of FGG (Fibrinogen gamma chain)
Q91H (p.Gln91His) 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.
Q91H (p.Gln91His) variant details
- p.Gln91His
- TOPMed rs1310562266
- gnomAD rs1310562266
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.23
- CADD 14.40
- PolyPhen-2 0.57
- SIFT 0.05
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available