Variant information

Systematic Name c.881_902del22
Protein name p.Arg294fs
Mutation type frameshift insertion or deletion
Domain TRD
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.881_902del22 p.Arg294fs frameshift insertion or deletion TRD Mutation associated with disease Female Rett syndrome-not certain 3605