Variant information
Systematic Name (NM_004992.3:) |
c.674C>T |
---|---|
Protein name (NP_004983) |
p.Pro225Leu |
Alternate systematic Name (NM_001110792.1:) |
c.710C>T |
Alternate Protein name (NP_001104262) |
p.(Pro237Leu) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296605G>A |
Mutation type | Missense |
Domain | TRD |
Pathogenicity | Unknown |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.674C>T | p.Pro225Leu | Male | Rett syndrome-Male variant | 1659 | Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2):Moog, Ute, Smeets, Eric E. J., Van Roozendaal, Kees E. P., Schoenmakers, Sam, Herbergs, Jos, Schoonbrood-Lessen, Anneke M. J., Schrander-Stumpel, Connie T. R. M.:European Journal of Paediatric Neurology: 12615169 | View details |
2 | c.674C>T | p.Pro225Leu | Female | Rett syndrome-Classical | 2429 | Rett syndrome in Spain: mutation analysis and clinical correlations:Monros, E., Armstrong J., Aibar, E., Poo, P., Canós, I., Pineda, M.:Brain and Development: 11738885 | View details |