Y117H (p.Tyr117His) variant of MEF2C (Q06413)
Y117H (p.Tyr117His) 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.
Y117H (p.Tyr117His) variant details
- p.Tyr117His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available