Variant information
Systematic Name (NM_004992.3:) |
c.667A>T |
---|---|
Protein name (NP_004983) |
p.Lys223* |
Alternate systematic Name (NM_001110792.1:) |
c.703A>T |
Alternate Protein name (NP_001104262) |
p.(Lys235*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296612T>A |
Mutation type | nonsense |
Domain | TRD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.667A>T | p.Lys223* | Female | Rett syndrome-classical | 6612 | ::: | View details |