Variant information
Systematic Name (NM_004992.3:) |
c.880_884del5 |
---|---|
Protein name (NP_004983) |
p.Arg294fs |
Alternate systematic Name (NM_001110792.1:) |
c.916_920del5 |
Alternate Protein name (NP_001104262) |
p.(Arg306Cysfs*35) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296395_153296399del5 |
Mutation type | Frameshift insertion or deletion |
Domain | TRD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.880_884del5 | p.Arg294fs | Female | Rett syndrome-Not certain | 1254 | Influence of mutation type and location on phenotype in 123 patients with Rett syndrome:Huppke, P., Held, M., Hanefeld, F., Engel, W., Laccone, F.:Neuropediatrics: 12075485 | View details |