L65M (p.Leu65Met) variant of KRT14 (Keratin, type I cytoskeletal 14)
L65M (p.Leu65Met) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
L65M (p.Leu65Met) variant details
- p.Leu65Met
- 1000Genomes rs3826551
- ESP rs3826551
- ExAC rs3826551
- TOPMed rs3826551
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available