G50D (p.Gly50Asp) variant of FGG (Fibrinogen gamma chain)
G50D (p.Gly50Asp) in FGG (Fibrinogen gamma chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G50D (p.Gly50Asp) variant details
- p.Gly50Asp
- NCI-TCGA Cosmic COSV6019
- cosmic curated COSV60196
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available