Variant information



Systematic Name c.377+95G>A
Protein name intronic variation
Mutation type Intronic variation
Domain Intronic
Pathogenicity Polymorphism not causing disease

Matching entries in the proband database


No: Systematic Name Protein name Mutation type Domain Pathogenicity Gender Phenotype Proband id
1 c.377+95G>A intronic variation Intronic variation Intronic Polymorphism not causing disease Male Not Rett synd. 1563
2 c.377+95G>A intronic variation Intronic variation Intronic Polymorphism not causing disease Female Not Rett synd. 1586