Variant information
Systematic Name (NM_004992.3:) |
c.1167_1200del34 |
---|---|
Protein name (NP_004983) |
p.Pro390fs |
Alternate systematic Name (NM_001110792.1:) |
c.1203_1236del34 |
Alternate Protein name (NP_001104262) |
p.(Pro402Alafs*8) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296079_153296112del34 |
Mutation type | Frameshift insertion or deletion |
Domain | C-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1167_1200del34 | p.Pro390fs | Female | Rett syndrome-Not certain | 1259 | 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 |