S62G (p.Ser62Gly) variant of KRT17 (Keratin, type I cytoskeletal 17)
S62G (p.Ser62Gly) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
S62G (p.Ser62Gly) variant details
- p.Ser62Gly
- ExAC rs11553455
- gnomAD rs11553455
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available