G42V (p.Gly42Val) variant of FGG (Fibrinogen gamma chain)
G42V (p.Gly42Val) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.82 / 1. The record also includes population frequency data and structural context.
G42V (p.Gly42Val) variant details
- p.Gly42Val
- gnomAD rs1173725188
- Missense
- Variant Prioritization Score for Impact Estimate 0.819
- REVEL 0.82
- CADD 29.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available