G111D (p.Gly111Asp) variant of KRT12 (Keratin, type I cytoskeletal 12)
G111D (p.Gly111Asp) in KRT12 (Keratin, type I cytoskeletal 12) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G111D (p.Gly111Asp) variant details
- p.Gly111Asp
- NCI-TCGA Cosmic COSV9928
- TOPMed rs1907047913
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available