Variant information



Systematic Name c.326dupA
Protein name p.Gln110fs
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.326dupA p.Gln110fs frameshift insertion or deletion MBD Mutation associated with disease Female Rett syndrome-Classical 4347