Variant information

Systematic Name c.711_1269del559
Protein name p.Gly238fs
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.711_1269del559 p.Gly238fs frameshift insertion or deletion TRD Mutation associated with disease Female Rett syndrome-not certain 3266