F101L (p.Phe101Leu) variant of KRT12 (Keratin, type I cytoskeletal 12)
F101L (p.Phe101Leu) in KRT12 (Keratin, type I cytoskeletal 12) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
F101L (p.Phe101Leu) variant details
- p.Phe101Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available