Variant information
Systematic Name (NM_004992.3:) |
c.420delG |
---|---|
Protein name (NP_004983) |
p.Tyr141fs |
Alternate systematic Name (NM_001110792.1:) |
c.456delG |
Alternate Protein name (NP_001104262) |
p.(Tyr153Thrfs*5) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296859delC |
Mutation type | frameshift insertion or deletion |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.420delG | p.Tyr141fs | Female | Rett syndrome-Classical | 4362 | Identification and characterization of novel sequence variations in MECP2 gene in Rett syndrome patients:Monnerat, L.S., Moreira, A.D.S., Alves,M.C.V., Bonvicino, C.R., Vargas, F.R.:Brain & Development: 20031356 | View details |