CDKL5 Proband Entry

Entry ID: cp190

Systematic name: c.978-23T>C

Protein name: p.=

Alternate name(s): intronic variation

Mutation type: intronic variant

Domain: not specified

Pathogenicity class: benign variant

Gender: Male

Phenotype: Not Rett syndrome - neonatal seizures, severe epilepsy and mental retardation

Other mutation:

X-inactivation results: Not applicable

Chromosomal abnormality: Not known

Method of testing: direct, exons 2-21

Source of DNA: blood

Familial testing: inherited from unaffected mother

Familial X-inactivation:

Control screening: not found in 306/306 chromosomes

dbSNP ID: rs267608555

Source: 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

Publication ID:


Entry last updated on: 2018-06-05 13:45:42

Similar entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.978-23T>C p.= Not known - unaffected family member Female 20397747 White et al (2010) cp191

Displaying a total number of 1 proband entries.