Variant information
Systematic Name (NM_004992.3:) |
c.829delG |
---|---|
Protein name (NP_004983) |
p.Ala277fs |
Alternate systematic Name (NM_001110792.1:) |
c.865delG |
Alternate Protein name (NP_001104262) |
p.(Ala289Glnfs*12) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296450delC |
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.829delG | p.Ala277fs | Female | Rett syndrome-classical | 6631 | ::: | View details |