H140Q (p.His140Gln) variant of KRT13 (Keratin, type I cytoskeletal 13)
H140Q (p.His140Gln) 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 structural context.
H140Q (p.His140Gln) variant details
- p.His140Gln
- 1000Genomes rs530596803
- ExAC rs530596803
- TOPMed rs530596803
- gnomAD rs530596803
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available