D91N (p.Asp91Asn) variant of KRT13 (Keratin, type I cytoskeletal 13)
D91N (p.Asp91Asn) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D91N (p.Asp91Asn) variant details
- p.Asp91Asn
- NCI-TCGA Cosmic COSV5583
- cosmic curated COSV55839
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available