Variant information

Systematic Name c.226delG
Protein name p.Glu76fs
Mutation type frameshift insertion or deletion
Domain MBD
Pathogenicity Mutation associated with disease

Matching entries in the proband database

No: Systematic Name Protein name Mutation type Domain Pathogenicity Gender Phenotype Proband id
1 c.226delG p.Glu76fs frameshift insertion or deletion MBD Mutation associated with disease Female Rett syndrome-classical 6641