Variant information



Systematic Name c.483delG
Protein name p.Arg162fs
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.483delG p.Arg162fs Frameshift insertion or deletion MBD Mutation associated with disease Female Rett syndrome-Not certain 1888