CDKL5 Variant
Systematic name: c.400C>T
Protein name: p.Arg134*
Alternate name(s): p.R134X
Mutation type: nonsense
Domain: serine-threonine kinase site
Pathogenicity class: pathogenic variant
dbSNP ID: rs267608472
First reference: Rademacher, N., Hambrock, M., Fischer, U., Moser, B., Ceulemans, B., Lieb, W., Boor, R., Stefanova, I., Gillessen-Kaesbach, G., Runge, C., Korenke, G.C., Spranger, S., Laccone, F., Tzschach, A., Kalscheuer, V.M. (2011) Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features. Neurogenetics 12:165-167. Pubmed ID: 21318334
Comments:
Variant last updated on: 2018-06-05 14:40:30
Matching entries in the proband database
cDNA name | Protein name | Phenotype | Gender | Reference | Proband ID |
---|---|---|---|---|---|
c.400C>T | p.Arg134* | Not Rett syndrome - early-onset seizures and mental retardation | Female | 21318334, Rademacher et al (2011) | cp223 |
c.400C>T | p.Arg134* | Not Rett syndrome - epileptic encephalopathy | Female | 22678952, Bahi-Buisson et al (2012) | cp457 |
Displaying a total number of 2 proband entries matching this variant.