A29V (p.Ala29Val) variant of FGG (Fibrinogen gamma chain)
A29V (p.Ala29Val) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
A29V (p.Ala29Val) variant details
- p.Ala29Val
- TOPMed rs1025420920
- gnomAD rs1025420920
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- REVEL 0.15
- CADD 23.50
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available