G79C (p.Gly79Cys) variant of KRT3 (Keratin, type II cytoskeletal 3)
G79C (p.Gly79Cys) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G79C (p.Gly79Cys) variant details
- p.Gly79Cys
- NCI-TCGA Cosmic COSV1005
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available