Variant information
Systematic Name (NM_004992.3:) |
c.1164_1184delinsCTGAGCCCCAGGACTTGAGCA |
---|---|
Protein name (NP_004983) |
p.Pro389* |
Alternate systematic Name (NM_001110792.1:) |
c.1200_1220delinsCTGAGCCCCAGGACTTGAGCA |
Alternate Protein name (NP_001104262) |
p.(Pro401*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296095_153296115delinsTGCTCAAGTCCTGGGGCTCAG |
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.1164_1184delinsCTGAGCCCCAGGACTTGAGCA | p.Pro389* | Female | Not Rett synd. | 5301 | Brief report: MECP2 mutations in people without Rett syndrome:Suter, B., Treadwell-Deering, D., Zoghbi, H.Y., Glaze, D.G., Neul, J.L.:J Autism Dev Disord: 23921973 | View details |
2 | c.1164_1184delinsCTGAGCCCCAGGACTTGAGCA | p.Pro389* | Female | Rett syndrome-atypical | 4821 | Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation:Corbani, S., Chouery, E., Fayyad, J., Fawaz, A., El Tourjuman, O., Badens, C., Lacoste, C., Delague, V., Megarbane, A.:Journal of Intellectual Disability Research: 21954873 | View details |