CDKL5 Proband Entry



Entry ID: cp130

Systematic name: c.99+29T>G

Protein name: p.=

Alternate name(s): intronic variation

Mutation type: intronic variant

Domain: ATP binding region

Pathogenicity class: variant of uncertain significance

Gender: Unknown

Phenotype: Not known

Other mutation:

X-inactivation results: Not known

Chromosomal abnormality: Not known

Method of testing: DHPLC, MECP2, CDKL5

Source of DNA: blood

Familial testing: No

Familial X-inactivation:

Control screening: No

dbSNP ID: rs267608422

Source: Russo, S., Marchi, M., Cogliati, F., Bonati, M.T., Pintaudi, M.,Veneselli, E., Saletti, V., Balestrini, M., Ben-Zeev, B., Larizza, L. (2009) Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes. Neurogenetics 10:241-250. Pubmed ID: 19241098

Publication ID:

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.