Variant information
Systematic Name (NM_004992.3:) |
c.488_1189del702 |
---|---|
Protein name (NP_004983) |
p.Gly163_Ser396del |
Alternate systematic Name (NM_001110792.1:) |
c.524_1225del702 |
Alternate Protein name (NP_001104262) |
p.(Gly175_Ser408del) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296090_153296791del702 |
Mutation type | in-frame insertion or deletion |
Domain | inter-domain region |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.488_1189del702 | p.Gly163_Ser396del | Female | Rett syndrome-not certain | 3261 | Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update:Philippe C, Villard L, de Roux N, Raynaud M, Bonnefond JP, Pasquier L, Lesca G, Mancini J, Jonveaux P, Moncla A, Chelly J, Bienvenu T:European Journal of Medical Genetics: 16473305 | View details |