A146D (p.Ala146Asp) variant of KRT13 (Keratin, type I cytoskeletal 13)
A146D (p.Ala146Asp) 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.
A146D (p.Ala146Asp) variant details
- p.Ala146Asp
- 1000Genomes rs760134
- ESP rs760134
- ExAC rs760134
- TOPMed rs760134
- Benign
- Missense
- EBI: Benign (in dbSNP:rs760134)
- UniProt: Benign (in dbSNP:rs760134)
- Population evidence available
- Structural context available