Variant information
Systematic Name (NM_004992.3:) |
c.739delG |
---|---|
Protein name (NP_004983) |
p.Val247fs |
Alternate systematic Name (NM_001110792.1:) |
c.775delG |
Alternate Protein name (NP_001104262) |
p.(Val259*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296540delC |
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.739delG | p.Val247fs | Female | Rett syndrome-classical | 1930 | Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome:Schanen, C., Houwink, EJ., Dorrani, N., Lane, J., Everett, R., Feng, A., Cantor, RM. and Percy, A:American Journal of Medical Genetics: 15057977 | View details |