CDKL5 Proband Entry

Entry ID: cp104

Systematic name: c.1892T>C

Protein name: p.Ile631Thr

Alternate name(s): p.I631T

Mutation type: missense

Domain: not specified

Pathogenicity class: likely benign variant

Gender: Female

Phenotype: Not known - unaffected family member

Other mutation:

X-inactivation results: Yes - random

Chromosomal abnormality: Not known

Method of testing: direct, exons 1-21

Source of DNA: blood

Familial testing: found in daughter wth early-onset encephalopathy

Familial X-inactivation:

Control screening: No

dbSNP ID: rs144878564

Source: Nemos, C., Lambert, L., Giuliano, F., Doray, B., Roubertie, A., Goldenberg, A., Delobel, B., Lyet, V., N'guyen, M.A., Saunier, A., Verneau, F., Jonveaux, P., Philippe, C (2009) Mutation spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature. Clinical Genetics 76:357-371. Pubmed ID: 19793311

Publication ID:


Entry last updated on: 2014-05-09 06:14:58

Similar entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.1892T>C p.Ile631Thr Not Rett syndrome - early-onset encephalopathy Female 19793311 Nemos et al (2009) cp102

Displaying a total number of 1 proband entries.