Variant information
Systematic Name (NM_004992.3:) |
c.1158_1186del29insCCA |
---|---|
Protein name (NP_004983) |
p.Pro387Hisfs*9 |
Alternate systematic Name (NM_001110792.1:) |
c.1194_1222delinsCCA |
Alternate Protein name (NP_001104262) |
p.(Pro399Hisfs*9) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296093_153296121delinsTGG |
Mutation type | frameshift combined insertion and 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.1158_1186del29insCCA | p.Pro387Hisfs*9 | Female | Rett syndrome-not certain | 3610 | MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome:Li, M.-R., Pan, H., Bao, X.-H., Zhang, Y.-Z., Wu, X.-R.:Journal of Human Genetics: 17089071 | View details |