V148F (p.Val148Phe) variant of FGG (Fibrinogen gamma chain)
V148F (p.Val148Phe) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
V148F (p.Val148Phe) variant details
- p.Val148Phe
- gnomAD rs1450821105
- Missense
- Variant Prioritization Score for Impact Estimate 0.173
- REVEL 0.25
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.71
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available