Variant information
Systematic Name (NM_004992.3:) |
c.1069_1071delAGC |
---|---|
Protein name (NP_004983) |
p.Ser357del |
Alternate systematic Name (NM_001110792.1:) |
c.1105_1107delAGC |
Alternate Protein name (NP_001104262) |
p.(Ser369del) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296208_153296210delGCT |
Mutation type | in-frame insertion or deletion |
Domain | c-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1069_1071delAGC | p.Ser357del | Female | Rett syndrome-Classical | 2622 | Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms:Zahorakova, D., Rosipal, R., Hadac, J., Zumrova, A., Bzduch, V., Misovicova, N., Baxova, A., Zeman, J., Martasek, P.:Journal of Human Genetics: 17387578 | View details |