CDKL5 Variant



Variant ID: cm266

Systematic name: c.364G>A

Protein name: p.Ala122Thr

Alternate name(s):

Mutation type: missense

Domain: catalytic domain

Pathogenicity class: variant of uncertain significance

dbSNP ID:

First reference: Fehr S,Leonard H, Ho G, Williams S, de Klerk N, Forbes D, Christodoulou J, Downs J (2015) There is variability in the attainment of developmental milestones in the CDKL5 disorder. J Neurodev Disord. 7:2. Pubmed ID: 25657822

Comments:

Variant last updated on: 2018-10-23 12:21:11

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.364G>A p.Ala122Thr Not Rett syndrome Female 25657822, Fehr S et al (2015) cp549

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