Variant information
Systematic Name (NM_004992.3:) |
c.451delG |
---|---|
Protein name (NP_004983) |
p.Asp151fs |
Alternate systematic Name (NM_001110792.1:) |
c.487delG |
Alternate Protein name (NP_001104262) |
p.(Asp163Thrfs*9) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296828delC |
Mutation type | Frameshift insertion or deletion |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.451delG | p.Asp151fs | Unknown | Rett syndrome-atypical | 1526 | 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 |