CDKL5 Variant

Variant ID: cm185
Systematic name: c.2704C>T
Protein name: p.Gln902*
Alternate name(s): p.Q902X
Mutation type: nonsense
Domain: regulatory C-terminal
Pathogenicity class: pathogenic variant
First reference: Roche Martinez, A., Armstrong, J., Gerotina, E., Fons, C., Campistol, J., Pineda, M. (2012) CDKL5 in different atypical Rett syndrome variants: description of the first eight patients from Spain. Journal of Pediatric Epilepsy 1:27-35


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.2704C>T p.Gln902* Rett syndrome - atypical, early onset seizures Female Roche Martinez et al (2012) cp379

Displaying a total number of 1 proband entries matching this variant.