Variant information
Systematic Name (NM_004992.3:) |
c.430A>T |
---|---|
Protein name (NP_004983) |
p.Lys144* |
Alternate systematic Name (NM_001110792.1:) |
c.466A>T |
Alternate Protein name (NP_001104262) |
p.(Lys156*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296849T>A |
Mutation type | nonsense |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.430A>T | p.Lys144* | Female | Rett syndrome-Not certain | 1064 | 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.430A>T | p.Lys144* | Female | Rett syndrome-Classical | 2580 | Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms:Zahorakova, D., Rosipal, R., Hadac, J., Zumrova, A., Bzduch, V., Misovicova, N., Baxova, A., Zeman, J., Martasek, P.:Journal of Human Genetics: 17387578 | View details |