CDKL5 Proband Entry
Entry ID: cp380
Systematic name: c.2927C>T
Protein name: p.Pro976Leu
Alternate name(s): p.P976L
Mutation type: missense
Domain: regulatory C-terminal
Pathogenicity class: likely benign variant
Gender: Female
Phenotype: Rett syndrome - atypical, late regression
Other mutation:
X-inactivation results: Yes - 46:54
Chromosomal abnormality: No
Method of testing: direct, MECP2 negative, CDKL5 Ex1-22
Source of DNA: not stated
Familial testing: de novo
Familial X-inactivation:
Control screening: not found in 200/200 chromosomes
dbSNP ID:
Source: Roche Martinez, A., Armstrong, J., Gerotina, E., Fons, C., Campistol, J., Pineda, M. (2012) CDKL5 in different atypical Rett syndrome variants: description of the first eight patients from Spain. Journal of Pediatric Epilepsy 1:27-35
Comments:
Entry last updated on: 2018-06-05 13:45:42
Similar entries in the proband database
There are no other entries in the database with a similar genotype.