Variant information


Systematic Name
(NM_004992.3:)		 c.1433G>A
Protein name
(NP_004983)		 p.Arg478Gln
Alternate systematic Name
(NM_001110792.1:)		 c.1469G>A
Alternate Protein name
(NP_001104262)		 p.(Arg490Gln)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153295846C>T
Mutation type missense
Domain C-term
Pathogenicity Polymorphism not causing disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.1433G>A p.Arg478Gln Female Not Rett synd. 5225 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