S99L (p.Ser99Leu) variant of FGG (Fibrinogen gamma chain)
S99L (p.Ser99Leu) 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.
S99L (p.Ser99Leu) variant details
- p.Ser99Leu
- NCI-TCGA Cosmic COSV6019
- cosmic curated COSV60196
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available