Variant information
Systematic Name (NM_004992.3:) |
c.1250A>T |
---|---|
Protein name (NP_004983) |
p.Lys417Met |
Alternate systematic Name (NM_001110792.1:) |
c.1286A>T |
Alternate Protein name (NP_001104262) |
p.(Lys429Met) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296029T>A |
Mutation type | missense |
Domain | C-term |
Pathogenicity | Unknown |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1250A>T | p.Lys417Met | Male | Not Rett synd. | 2796 | Early progressive encephalopathy in boys and MECP2 mutations:Kankirawatana, P., Leonard, H., Ellaway, C., Scurlock, J., Mansour, A., Makris, C.M., Dure, L.S., IV, Friez, M., Lane, J., Kiraly-Borri, C., Fabian, V., Davis, M., Jackson, J., Christodoulou, J., Kaufmann, W.E., Ravine, D., Percy, A.K.":Neurology: 16832102 | View details |
2 | c.1250A>T | p.Lys417Met | Female | Not Rett synd. | 4675 | Early progressive encephalopathy in boys and MECP2 mutations:Kankirawatana, P., Leonard, H., Ellaway, C., Scurlock, J., Mansour, A., Makris, C.M., Dure, L.S., IV, Friez, M., Lane, J., Kiraly-Borri, C., Fabian, V., Davis, M., Jackson, J., Christodoulou, J., Kaufmann, W.E., Ravine, D., Percy, A.K.:Neurology: 16832102 | View details |
3 | c.1250A>T | p.Lys417Met | Male | Not Rett synd. | 6619 | ::: | View details |