Variant information



Systematic Name c.[377+22C>G(;)378-74C>T]
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+22C>G(;)378-74C>T] intronic variation Intronic variation Intronic Polymorphism not causing disease Female Not Known 2045