CDKL5 Variant



   CSV explantation text


Variant ID: cm224
Systematic name: c.234delA
Protein name: p.Arg80Valfs*33
Alternate name(s): p.R80fs
Mutation type: frameshift insertion and/or deletion
Domain: catalytic domain
Pathogenicity class: pathogenic variant
dbSNP ID:

First reference: Zhao, Y., Zhang, X., Bao, X., Zhang, Q., Zhang, J., Cao, G., Zhang, J., Li, J., Wei, L., Pan, H., Wu, X. (2014) Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients. BMC Medical Genetics 15:24. Pubmed ID: 24564546

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.234delA p.Arg80Valfs*33 Not Rett syndrome - early-onset epileptic encephalopathy Female 24564546, Zhao et al (2014) cp451

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