CDKL5 Proband Entry



Entry ID: cp430

Systematic name: c.1741C>T

Protein name: p.His581Tyr

Alternate name(s): p.H581Y

Mutation type: missense

Domain: not specified

Pathogenicity class: variant of uncertain significance

Gender: Unknown

Phenotype: Not Rett syndrome - uncertain

Other mutation:

X-inactivation results: No

Chromosomal abnormality: Not known

Method of testing: targeted sequencing, 65 genes, CDKL5 covered at ~95% at >25x

Source of DNA: not stated

Familial testing: No

Familial X-inactivation:

Control screening: No

dbSNP ID:

Source: Carvill, G.L., Heavin, S.B., Yendle, S.C., McMahon, J.M., O'Roak, B.J., Cook, J., Khan, A., Dorschner, M.O., Waver, M., Calbert, S., Malone, S., Wallace, G., Stanley, T., Bye, A.M.E., Bleasel, A., Howell, K.B., Kivity, S., Mackay, M.T., Rodriguez-Casero, V., Webster, R., Korczyn, A., Afawi, Z., Zelnick, N., Lerman-Sagie, T., Lev, D., Moller, R.S., Gill, D., Andrade, D.M., Freeman, J.L., Saleir, L.G., Shendure, J., Berkovic, S.F., Scheffer, I.E., Mefford, H.C. (2013) Targeted resequencing in epileptic encephalopathies identified de novo mutations in CHD2 and SYNGAP1. Nature Genetics 45:825-830. Pubmed ID: 23708187

Publication ID: T22652

Comments: Listed in Supplementary Table 1

Entry last updated on: 2014-10-31 04:40:12

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