Variant information
Systematic Name (NM_004992.3:) |
c.[881_1169del289; 1189_1196del8] |
---|---|
Protein name (NP_004983) |
p.Arg294_Asp398delinsHisLeuSerProArgAla |
Alternate systematic Name (NM_001110792.1:) |
c.[917_1205del289;1225_1232del8] |
Alternate Protein name (NP_001104262) |
p.? |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.[153296110_153296398del289;153296083_153296090del8] |
Mutation type | In-frame insertion or deletion, frameshift insertion or deletion |
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.[881_1169del289; 1189_1196del8] | p.Arg294_Asp398delinsHisLeuSerProArgAla | Unknown | Rett syndrome-classical | 1528 | Molecular analysis of Japanese patients with Rett syndrome: identification of five novel mutations and genotype-phenotype correlation:Yamada, Yasukazu, Miura, Kiyokuni, Kumagai, Toshiyuki, Hayakawa, Chiemi, Miyazaki, Shuji, Matsumoto, Akiko, Kurosawa, Kenji, Nomura, Noriko, Taniguchi, Hiroko, Sonta, Shin-ichi, Yamanaka, Tsutomu, and Wakamatsu, Nobuaki:Human mutation: 11524741 | View details |