Variant information
Systematic Name (NM_004992.3:) |
c.409_1158del |
---|---|
Protein name (NP_004983) |
p.Glu137_Leu386del |
Alternate systematic Name (NM_001110792.1:) |
c.445_1194del |
Alternate Protein name (NP_001104262) |
p.(Glu149_Leu398del) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296121_153296870del |
Mutation type | in-frame insertion or deletion |
Domain | MBD, inter-domain region, TRD, TRD-NLS, C-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.409_1158del | p.Glu137_Leu386del | Female | Rett syndrome-classical | 4866 | Molecular diagnostic dilemmas in Rett syndrome:Zvereff, V., Carpenter, L., Patton, D., Cabral, H., Rita, D., Wilson, A., Anyane-Yeboa, K., White, L., Friedman, K.J.:Brain & Development: 22277191 | View details |