Variant information
Systematic Name (NM_004992.3:) |
c.378-?_1337+?del |
---|---|
Protein name (NP_004983) |
p.Asn126fs |
Alternate systematic Name (NM_001110792.1:) |
c.414_1373del |
Alternate Protein name (NP_001104262) |
p.(Pro139_Ala458del) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153295942_153296901del |
Mutation type | exon deletion |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.378-?_1337+?del | p.Asn126fs | Female | Rett syndrome-classical | 2786 | 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 |
2 | c.378-?_1337+?del | p.Asn126fs | Female | Rett syndrome-classical | 2792 | 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 |