Variant information
Systematic Name (NM_004992.3:) |
c.[334A>T(;)871T>G] |
---|---|
Protein name (NP_004983) |
p.[Lys112*(;)Ser291Ala] |
Alternate systematic Name (NM_001110792.1:) |
c.[370A>T;907T>G] |
Alternate Protein name (NP_001104262) |
p.? |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.[153297701T>A;153296408A>C] |
Mutation type | nonsense, missense |
Domain | MBD, TRD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.[334A>T(;)871T>G] | p.[Lys112*(;)Ser291Ala] | Female | Rett syndrome-Classical | 4230 | Genotype-phenotype correlation in Brazillian Rett syndrome patients:de Lima, F.T., Brunoni, D., Schwartzman, J.S., Pozzi, M.C., Kok, F., Juliano, Y., Pereira, L.V.:Arq Neuropsiquiatr: 19722030 | View details |