F26C (p.Phe26Cys) variant of MEF2C (Q06413)
F26C (p.Phe26Cys) in MEF2C (Q06413) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F26C (p.Phe26Cys) variant details
- p.Phe26Cys
- NCI-TCGA Cosmic COSV6093
- cosmic curated COSV60939
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available