Variant information
Systematic Name (NM_004992.3:) |
c.1162_1179del18 |
---|---|
Protein name (NP_004983) |
p.Pro388_Pro393del |
Alternate systematic Name (NM_001110792.1:) |
c.1198_1215del18 |
Alternate Protein name (NP_001104262) |
p.(Pro400_Pro405del) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296100_153296117del18 |
Mutation type | in-frame insertion or deletion |
Domain | C-term |
Pathogenicity | Polymorphism not causing disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1162_1179del18 | p.Pro388_Pro393del | Female | Rett syndrome-Atypical | 2183 | :Cardiff, UK:: | View details |
2 | c.1162_1179del18 | p.Pro388_Pro393del | Male | Not Rett synd. | 4714 | Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations:Hadzsiev, K., Polgar, N., Bene, J., Jomlosi, K., Karteszi, J., Hollody, K., Kosztolanyi, G., Renieri, A., Melegh, B.:Journal of Human Genetics: 21160487 | View details |