Proband information
Proband id | 4313 |
---|---|
Systematic Name (NM_004992.3:) |
c.1189G>T |
Protein name (NP_004983) |
p.Glu397* |
Alternate systematic Name (NM_001110792.1:) |
c.1225G>T |
Alternate Protein name (NP_001104262) |
p.(Glu409*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296090C>A |
Mutation type | nonsense |
Domain | C-term |
Pathogenicity | Mutation associated with disease |
Evidence of Pathogenicity | |
Detection | direct |
Extent | exons 2-4 |
Source of DNA | blood |
Carrier | N |
Carrier result | |
Other mutations | NK |
X-inactivation results | |
X-inactivation relatives | |
Gender | Female |
Sporadic/Familial | sporadic |
Phenotype-class | Rett syndrome-not certain |
Reference | Spectrum of MECP2 mutations in New Zealand Rett syndrome patients:Raizis, A.M., Saleem, M., MacKay, R., George, P.M.:New Zealand Medical Journal: 19652677 |
Matching entries in the proband database
No: | Systematic Name | Protein name | Gender | Carrier result | Phenotype | Proband id | Reference |
---|---|---|---|---|---|---|---|
1 | c.1189G>T | p.Glu397* | Female | Rett syndrome-not certain | 4313 | Spectrum of MECP2 mutations in New Zealand Rett syndrome patients:Raizis, A.M., Saleem, M., MacKay, R., George, P.M.:New Zealand Medical Journal: 19652677 |