Variant information

Systematic Name
Protein name
Alternate systematic Name
Alternate Protein name
Genomic nomenclature
Mutation type Nonsense
Domain N-term
Pathogenicity Mutation associated with disease

View proband information

No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.146C>A p.Ser49* Unknown Rett syndrome-Not certain 236 A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients:Bourdon, Violaine, Philippe, Christophe, Labrune, Orianne, Amsallem, Daniel, Arnould, CÚcile, Jonveaux, Philippe:Human genetics: 11214906 View details
2 c.146C>A p.Ser49* Female Not Known 1755 :Friez, Michael:: View details
3 c.146C>A p.Ser49* Female Rett syndrome-Atypical 2338 :Cardiff, UK:: View details
4 c.146C>A p.Ser49* Female Rett syndrome-classical 6602 ::: View details