G67C (p.Gly67Cys) variant of KRT13 (Keratin, type I cytoskeletal 13)
G67C (p.Gly67Cys) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
G67C (p.Gly67Cys) variant details
- p.Gly67Cys
- 1000Genomes rs141310122
- ESP rs141310122
- ExAC rs141310122
- TOPMed rs141310122
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available