Variant information
Systematic Name (NM_004992.3:) |
c.301C>T |
---|---|
Protein name (NP_004983) |
p.Pro101Ser |
Alternate systematic Name (NM_001110792.1:) |
c.337C>T |
Alternate Protein name (NP_001104262) |
p.(Pro113Ser) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153297734G>A |
Mutation type | Missense |
Domain | MBD |
Pathogenicity | Unknown |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.301C>T | p.Pro101Ser | Female | Rett syndrome-Classical | 1436 | Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females:Vacca, Marcella, Filippini, Francesco, Budillon, Alberta, Rossi, Valeria, Mercadante, Grazia, Manzati, Alberta, Gualandi, Francesca, Bigoni, Stefania, Trabanelli, Cecilia, Pini, Giorgio, Calzolari, Elisa, Ferlini, Alessandra, Meloni, Ilaria, Hayek, Giuseppe, Zappella, Michele, Renieri, Alessandra, D'Urso, Michele, D'Esposito, Maurizio, MacDonald, Fiona, Kerr, Alison, Dhanjal, Seema, Hultén, Maj:Journal of Molecular Medicine: 11269512 | View details |
2 | c.301C>T | p.Pro101Ser | Female | Not Known | 1687 | :Friez, Michael:: | View details |
3 | c.301C>T | p.Pro101Ser | Female | Rett syndrome-Not certain | 1822 | :Bunyan, D.:: | View details |
4 | c.301C>T | p.Pro101Ser | Female | Rett syndrome-Atypical | 2169 | :Cardiff, UK:: | View details |