Variant information
Systematic Name (NM_004992.3:) |
c.1327G>A |
---|---|
Protein name (NP_004983) |
p.Ala443Thr |
Alternate systematic Name (NM_001110792.1:) |
c.1363G>A |
Alternate Protein name (NP_001104262) |
p.(Ala455Thr) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153295952C>T |
Mutation type | missense |
Domain | C-term |
Pathogenicity | Unknown |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1327G>A | p.Ala443Thr | Male | Not Rett synd. | 4897 | Molecular diagnostic dilemmas in Rett syndrome:Zvereff, V., Carpenter, L., Patton, D., Cabral, H., Rita, D., Wilson, A., Anyane-Yeboa, K., White, L., Friedman, K.J.:Brain & Development: 22277191 | View details |
2 | c.1327G>A | p.Ala443Thr | Female | Not Rett synd. | 4898 | Molecular diagnostic dilemmas in Rett syndrome:Zvereff, V., Carpenter, L., Patton, D., Cabral, H., Rita, D., Wilson, A., Anyane-Yeboa, K., White, L., Friedman, K.J.:Brain & Development: 22277191 | View details |