Variant information

Systematic Name c.1163_*39del338
Protein name p.Pro388fs
Mutation type Frameshift insertion or deletion
Domain C-term
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.1163_*39del338 p.Pro388fs Frameshift insertion or deletion C-term Mutation associated with disease Unknown Rett syndrome-Not certain 1362