CDKL5 Variant

   CSV explantation text

Variant ID: cm93
Systematic name: c.58G>C
Protein name: p.Gly20Arg
Alternate name(s): p.G20R
Mutation type: missense
Domain: ATP binding region
Pathogenicity class: likely pathogenic variant
dbSNP ID: rs267608418

First reference: White, R., Ho, G., Schmidt, S., Scheffer, I.E., Fischer, A., Yendle, S.C., Bienvenu, T., Nectoux, J., Ellaway, C.J., Darmanian, A., Tong, X., Cloosterman, D., Bennetts, B., Kalra, V., Fullston, T., Gecz, J., Cox, T.C., Christodoulou, J. (2010) Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disorders. Twin Res Hum Genet 13:168-178. Pubmed ID: 20397747

Comments: In silico prediction: SIFT = deleterious, MutationTaster = disease-causing, PolyPhen2 = probably damaging, AlignGVGD = benign (C0)

Variant last updated on: 2018-06-05 14:40:30

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.58G>C p.Gly20Arg Not Rett syndrome - epileptic encephalopathy Female 20397747, White et al (2010) cp142

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