CDKL5 Variant
Variant ID: cm262
Systematic name: c.38T>C
Protein name: p.Phe13Ser
Alternate name(s):
Mutation type: missense
Domain: N-terminal
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.38T>C | p.Phe13Ser | Not Rett syndrome | Female | 25657822, Fehr S et al (2015) | cp551 |
Displaying a total number of 1 proband entries matching this variant.