Variant information

Systematic Name c.1169-?_1170+?del
Protein name p.?
Mutation type exonic deletions
Domain C-term
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.1169-?_1170+?del p.? exonic deletions C-term Mutation associated with disease Female Rett syndrome-classical 3782