Variant information



Systematic Name c.677_678insA
Protein name p.Phe226fs
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.677_678insA p.Phe226fs Frameshift insertion or deletion TRD Mutation associated with disease Female Rett syndrome-Classical 944