R47G (p.Arg47Gly) variant of KRT8 (Keratin, type II cytoskeletal 8)
R47G (p.Arg47Gly) in KRT8 (Keratin, type II cytoskeletal 8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
R47G (p.Arg47Gly) variant details
- p.Arg47Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.