Variant information
Systematic Name (NM_004992.3:) |
c.1308_1309delTC |
---|---|
Protein name (NP_004983) |
p.Gln437fs |
Alternate systematic Name (NM_001110792.1:) |
c.1344_1345delTC |
Alternate Protein name (NP_001104262) |
p.(Gln449Alafs*49) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153295970_153295971delGA |
Mutation type | frameshift insertion or 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.1308_1309delTC | p.Gln437fs | Female | Rett syndrome-Not certain | 1122 | Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms:Buyse, Inge M., Fang, Ping, Hoon, Katherine T., Amir, Ruthie E., Zoghbi, Huda Y. and Roa, Benjamin B.:American Journal of Human Genetics: 11055898 | View details |
2 | c.1308_1309delTC | p.Gln437fs | Female | Rett syndrome-classical | 6642 | ::: | View details |