A89P (p.Ala89Pro) variant of FGG (Fibrinogen gamma chain)
A89P (p.Ala89Pro) in FGG (Fibrinogen gamma chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
A89P (p.Ala89Pro) variant details
- p.Ala89Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.207
- REVEL 0.31
- CADD 1.00
- PolyPhen-2 0.09
- SIFT 0.33
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available