CDKL5 Variant



Variant ID: cm3

Systematic name: c.145+17A>G

Protein name: p.=

Alternate name(s): intronic variation

Mutation type: intronic variant

Domain: catalytic domain

Pathogenicity class: benign variant

dbSNP ID: rs199814742

First reference: Tao, J., Van Esch, H., Hage-dorn-Greiwe, M., Hoffmann, K., Moser, B., Raynaud, M., Sperner, J., Fryns, J.-P., Schwinger, E., Gecz, J., Ropers, H.-H., Kalcheuer, V.M. (2004) Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation. Am J Hum Genet 75:1149-1154. Pubmed ID: 15499549

Comments: intronic polymorphism not predicted to affected splicing; often found in cis with c.3003C>G (p.H1001H) and c.3084G>A (p.T1028T)

Variant last updated on: 2014-03-13 05:37:22

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.[145+17A>G;3003C>T;3084G>A] p.= Rett syndrome - not certain Female 15499549, Tao et al (2004) cp5
c.[145+17A>G;3003C>T;3084G>A] p.= Unaffected - normal control Unknown 15499549, Tao et al (2004) cp6
c.[145+17A>G;3003C>T;3084G>A] p.= Unaffected - normal control Unknown 15499549, Tao et al (2004) cp7
c.[145+17A>G;3003C>T;3084G>A] p.= Not Rett syndrome - epilepsy, Rett-like Female 22867051, Maortua et al (2012) cp328
c.[145+17A>G;3003C>T;3084G>A] p.= Not Rett syndrome - epilepsy, Rett-like Female 22867051, Maortua et al (2012) cp329
[c.100-73C>T;c.145+17A>G; c.146-98A>G; c.404-57T>C; c.2153-47_2153-38del10; c.30 p.= Not Rett syndrome - epileptic encephalopathy Male 27187038, et al () cp500
[c.145+17A>G;c.146-98A>G;c.404-57T>C;c.2153-47_2153-38del10; c.3003C>T;c.3084G>A p.= Not Rett syndrome - West syndrome Male 27187038, et al () cp501

Displaying a total number of 7 proband entries matching this variant.