Variant information



Systematic Name c.377+2T>G
Protein name intronic variation
Mutation type Intronic variation
Domain Intronic
Pathogenicity Unknown

Matching entries in the proband database


No: Systematic Name Protein name Mutation type Domain Pathogenicity Gender Phenotype Proband id
1 c.377+2T>G intronic variation Intronic variation Intronic Unknown Unknown Rett syndrome-Not certain 1356