Variant information
Systematic Name (NM_004992.3:) |
c.799A>T |
---|---|
Protein name (NP_004983) |
p.Lys267* |
Alternate systematic Name (NM_001110792.1:) |
c.835A>T |
Alternate Protein name (NP_001104262) |
p.(Lys279*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296480T>A |
Mutation type | nonsense |
Domain | TRD-NLS |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.799A>T | p.Lys267* | Female | Rett syndrome-classical | 2889 | MECP2 mutations in Serbian Rett syndrome patients:Djarmati, A., Dobricic, V., Kecmanovic, M., Marsh, P., Jancic-Stefanovic, J., Klein, C., Djuric, M., Romac, S.:Acta Neurol Scand: 17986102 | View details |
2 | c.799A>T | p.Lys267* | Female | Rett syndrome-classical | 7038 | MECP2 mutation in a boy with severe apnea and sick sinus syndrome:Tsutomu Shioda ,Satoru Takahashi,Tadashi Kaname , Toyohiro Yamauchi, Tetsuya Fukuoka :Brain & Development: 29631775 | View details |