Variant information
Systematic Name (NM_004992.3:) |
c.750C>T |
---|---|
Protein name (NP_004983) |
p.Arg250Arg |
Alternate systematic Name (NM_001110792.1:) |
c.786C>T |
Alternate Protein name (NP_001104262) |
p.(=) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296529G>A |
Mutation type | silent |
Domain | TRD |
Pathogenicity | Silent polymorphism |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.750C>T | p.Arg250Arg | Female | Not Rett synd. | 1238 | MECP2 mutation screening in Swedish classical Rett syndrome females:Erlandson, A., Hallberg, B., Hagberg, B., Wahlström, and Martinsson, T.:European Child and Adolescent Psychiatry: 11469283 | View details |
2 | c.750C>T | p.Arg250Arg | Female | Rett syndrome-Not certain | 1633 | :Bunyan, D.:: | View details |
3 | c.750C>T | p.Arg250Arg | Unknown | Not Rett synd. | 5191 | MECP2 gene study in a large cohort testing of 240 female patients and 861 healthy controls (519 females and 342 males):Maortua, H., Martinez-Bouzas, C., Garcia-Ribes, A., Martinez, M.-J., Guillen, E., Domingo, M.-R., Calvo, M.-T., Guitart, M., Gabau, E., Botella, M.-P., Gener, B., Rubio, I., Lopez-Ariztegui, M.-A., Tejada, M.-I.:J Mol Diagn: 23810759 | View details |