Variant information

Systematic Name c.377+1G>T
Protein name intronic variation
Mutation type intronic variation
Domain intronic
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.377+1G>T intronic variation intronic variation intronic Mutation associated with disease Female Rett syndrome-classical 3763