CDKL5 Variant



   CSV explantation text


Variant ID: cm272
Systematic name: c.458A>T
Protein name: p. Asp153Val
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.458A>T p. Asp153Val Not Rett syndrome Female 25657822, Fehr S et al (2015) cp557

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