L69F (p.Leu69Phe) variant of KRT13 (Keratin, type I cytoskeletal 13)
L69F (p.Leu69Phe) 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.
L69F (p.Leu69Phe) variant details
- p.Leu69Phe
- NCI-TCGA Cosmic COSV5583
- cosmic curated COSV55839
- Ensembl rs1905027092
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available