Variant information

Systematic Name c.906delC
Protein name p.Ile303fs
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.906delC p.Ile303fs frameshift insertion or deletion TRD Mutation associated with disease Female Rett syndrome-not certain 3283