Variant information
Systematic Name (NM_004992.3:) |
c.1430G>C |
---|---|
Protein name (NP_004983) |
p.Ser477Thr |
Alternate systematic Name (NM_001110792.1:) |
c.1466G>C |
Alternate Protein name (NP_001104262) |
p.(Ser489Thr) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153295849C>G |
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.1430G>C | p.Ser477Thr | Male | Not Rett synd. | 394 | ::: | View details |
2 | c.1430G>C | p.Ser477Thr | Female | Not Rett synd. | 395 | ::: | View details |
3 | c.1430G>C | p.Ser477Thr | Unknown | Not Rett synd. | 2658 | Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation:Lesca, G., Bernard, V., Bozon, M., Touraine, R., Gérard, D., Edery, P., Calender, A.:European Journal of Medical Genetics: 17383248 | View details |