Variant information



Systematic Name c.1162_1163delCC
Protein name p.Pro388fs
Mutation type frameshift insertion or deletion
Domain C-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.1162_1163delCC p.Pro388fs frameshift insertion or deletion C-term Mutation associated with disease Female Not Known 4107