Variant information
Systematic Name (NM_004992.3:) |
c.439delG |
---|---|
Protein name (NP_004983) |
p.Asp147fs |
Alternate systematic Name (NM_001110792.1:) |
c.475delG |
Alternate Protein name (NP_001104262) |
p.(Asp159Thrfs*13) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296840delC |
Mutation type | Frameshift insertion or deletion |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.439delG | p.Asp147fs | Unknown | Rett syndrome-Not certain | 254 | 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, Cécile, Jonveaux, Philippe:Human genetics: 11214906 | View details |