Variant information
Systematic Name (NM_004992.3:) |
c.27-?_1185+?del |
---|---|
Protein name (NP_004983) |
p.Arg9fs |
Alternate systematic Name (NM_001110792.1:) |
c.63_1221del |
Alternate Protein name (NP_001104262) |
p.? |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296094_153298008del |
Mutation type | frameshift insertion or deletion |
Domain | N-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.27-?_1185+?del | p.Arg9fs | Female | Rett syndrome-classical | 2785 | Large deletions of the MECP2 gene in Chinese patients with classical Rett syndrome:Pan, H., Li, M.-R., Nelson, P., Bao, X.-H., Wu, X.-R., Yu, S.:Clinical Genetics: 17026625 | View details |