Variant information
Systematic Name (NM_004992.3:) |
c.1153_1190del |
---|---|
Protein name (NP_004983) |
p.Pro385Glyfs*7 |
Alternate systematic Name (NM_001110792.1:) |
c.1189_1226del38 |
Alternate Protein name (NP_001104262) |
p.(Pro397Glyfs*7) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296089_153296126del38 |
Mutation type | frameshift combined insertion and deletion |
Domain | C-term |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1153_1190del | p.Pro385Glyfs*7 | Female | Rett syndrome-classical | 7039 | MECP2 mutation in a boy with severe apnea and sick sinus syndrome:Tsutomu Shioda ,Satoru Takahashi,Tadashi Kaname , Toyohiro Yamauchi, Tetsuya Fukuoka :Brain & Development: 29631775 | View details |