CDKL5 Variant
Systematic name: c.64+2T>C
Protein name: p.?
Alternate name(s):
Mutation type: intronic variant
Domain: ATP binding region
Pathogenicity class: pathogenic variant
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.64+2T>C | p.? | Not Rett syndrome | Female | 25657822, Fehr S et al (2015) | cp567 |
Displaying a total number of 1 proband entries matching this variant.