Variant information
Systematic Name (NM_004992.3:) |
c.932C>T |
---|---|
Protein name (NP_004983) |
p.Thr311Met |
Alternate systematic Name (NM_001110792.1:) |
c.968C>T |
Alternate Protein name (NP_001104262) |
p.(Thr323Met) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296347G>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.932C>T | p.Thr311Met | Female | Rett syndrome-Not certain | 1858 | :Bunyan, D.:: | View details |
2 | c.932C>T | p.Thr311Met | Female | Rett syndrome-classical | 2817 | Diagnostic mutational analysis of MECP2 in Korean patients with Rett syndrome:Kim, I.-J., Kim, Y.-J., Son, B.-H., Nam, S.-O., Kang, H.-C., Kim, H.-D., Yoo, M.-A., Choi, O.-H., Kim, C.-M.:Experimental and Molecular Medicine: 16672765 | View details |
3 | c.932C>T | p.Thr311Met | Female | Not Rett synd. | 4888 | 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 |
4 | c.932C>T | p.Thr311Met | Female | Not Rett synd. | 4889 | 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 |