Variant information
Systematic Name (NM_004992.3:) |
c.734_759del26 |
---|---|
Protein name (NP_004983) |
p.Val245fs |
Alternate systematic Name (NM_001110792.1:) |
c.770_795del26 |
Alternate Protein name (NP_001104262) |
p.(Val257Glufs*5) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296520_153296545del26 |
Mutation type | frameshift insertion or deletion |
Domain | TRD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.734_759del26 | p.Val245fs | Female | Rett syndrome-classical | 2887 | MECP2 mutations in Serbian Rett syndrome patients:Djarmati, A., Dobricic, V., Kecmanovic, M., Marsh, P., Jancic-Stefanovic, J., Klein, C., Djuric, M., Romac, S.:Acta Neurol Scand: 17986102 | View details |