L12F (p.Leu12Phe) variant of FGG (Fibrinogen gamma chain)
L12F (p.Leu12Phe) 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.
L12F (p.Leu12Phe) variant details
- p.Leu12Phe
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10027
- NCI-TCGA Cosmic COSV6019
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available