Variant information



Systematic Name c.27-6026_1190delinsGT (deletion of exons 3 and 4)
Protein name p.Arg9fs
Mutation type frameshift combined insertion and deletion
Domain N-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.27-6026_1190delinsGT (deletion of exons 3 and 4) p.Arg9fs frameshift combined insertion and deletion N-term Mutation associated with disease Female Rett syndrome-not certain 3344