Variant information
Systematic Name (NM_004992.3:) |
c.748dupC |
---|---|
Protein name (NP_004983) |
p.Arg250fs |
Alternate systematic Name (NM_001110792.1:) |
c.784dupC |
Alternate Protein name (NP_001104262) |
p.(Arg262Profs*9) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296531dupG |
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.748dupC | p.Arg250fs | Female | Rett syndrome-Not certain | 33 | MeCP2 mutations in children with and without the phenotype of Rett Syndrome:Hoffbuhr, K., Devaney, J. M., LaFleur, B., Sirianni, N., Scacheri, C., Giron, J., Schuette, J., Innis, J., Marino, M., Philippart, M., Narayanan, V., Umansky, R., Kronn, D., Hoffman, E. P., and Naidu, S.:Neurology: 11402105 | View details |
2 | c.748dupC | p.Arg250fs | Female | Rett syndrome-Not certain | 1866 | :Bunyan, D.:: | View details |