Variant information
Systematic Name (NM_004992.3:) |
c.64A>T |
---|---|
Protein name (NP_004983) |
p.Lys22* |
Alternate systematic Name (NM_001110792.1:) |
c.100A>T |
Alternate Protein name (NP_001104262) |
p.(Lys34*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153297971T>A |
Mutation type | Nonsense |
Domain | N-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.64A>T | p.Lys22* | Female | Rett syndrome-Classical | 1404 | DHPLC analysis of the MECP2 gene in Italian Rett patients:Nicolao, Piero, Carella, Massimo, Giometto, Bruno, Tavolato, Bruno, Cattin, Riccardo, Giovannucci-Uzielli, Maria Luisa, Vacca, Marcella, Regione, Floriana Della, Piva, Stefania, Bortoluzzi, Stefania, Gasparini, Paolo:Human mutation: 11462237 | View details |
2 | c.64A>T | p.Lys22* | Female | Rett syndrome-Classical | 1459 | 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 |