C34G (p.Cys34Gly) variant of FGG (Fibrinogen gamma chain)
C34G (p.Cys34Gly) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
C34G (p.Cys34Gly) variant details
- p.Cys34Gly
- gnomAD rs1215202123
- Missense
- Variant Prioritization Score for Impact Estimate 0.768
- REVEL 0.84
- CADD 29.10
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 8.9e-05)
- Structural context available