F99I (p.Phe99Ile) variant of KRT1 (Keratin, type II cytoskeletal 1)
F99I (p.Phe99Ile) in KRT1 (Keratin, type II cytoskeletal 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F99I (p.Phe99Ile) variant details
- p.Phe99Ile
- NCI-TCGA TCGA novel
- Ensembl rs1941563473
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available