Variant information
Systematic Name (NM_004992.3:) |
c.[916C>T(;)984C>T] |
---|---|
Protein name (NP_004983) |
p.[Arg306Cys(;)Leu328Leu] |
Alternate systematic Name (NM_001110792.1:) |
c.[952C>T;1020C>T] |
Alternate Protein name (NP_001104262) |
p.? |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.[153296363G>A;153296295G>A] |
Mutation type | Missense, silent |
Domain | TRD, C-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.[916C>T(;)984C>T] | p.[Arg306Cys(;)Leu328Leu] | Female | Rett syndrome-Classical | 473 | ::: | View details |