F56C (p.Phe56Cys) variant of TBK1 (Q9UHD2)
F56C (p.Phe56Cys) in TBK1 (Q9UHD2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F56C (p.Phe56Cys) variant details
- p.Phe56Cys
- NCI-TCGA Cosmic COSV5915
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available