G71D (p.Gly71Asp) variant of KRT12 (Keratin, type I cytoskeletal 12)
G71D (p.Gly71Asp) 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 population frequency data and structural context.
G71D (p.Gly71Asp) variant details
- p.Gly71Asp
- rs771841418
- ExAC rs771841418
- TOPMed rs771841418
- gnomAD rs771841418
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available