C63W (p.Cys63Trp) variant of KRT14 (Keratin, type I cytoskeletal 14)
C63W (p.Cys63Trp) 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.
C63W (p.Cys63Trp) variant details
- p.Cys63Trp
- 1000Genomes rs11551758
- ExAC rs11551758
- TOPMed rs11551758
- gnomAD rs11551758
- Benign
- Missense
- EBI: Benign (in dbSNP:rs6503640)
- UniProt: Benign (in dbSNP:rs6503640)
- Structural context available