CDKL5 Variant



Variant ID: cm213

Systematic name: c.2896G>A

Protein name: p.Val966Ile

Alternate name(s): p.V966I

Mutation type: missense

Domain: regulatory C-terminal

Pathogenicity class: likely benign variant

dbSNP ID:

First reference: Das, D.K., Mehta, B., Menon, S.T., Raha, S., Udani, V. (2013) Novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene in Indian cases of Rett syndrome. Neuromol Med 15:218-225. Pubmed ID: 23242510

Comments: clinical significance uncertain, but unlikely to be pathogenic due to location (exon 20); in silico predictions: alignGVGD, SIFT, MutationTaster, Polyphen2 all benign

Variant last updated on: 2014-10-31 04:29:20

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.2896G>A p.Val966Ile Rett syndrome - atypical Female 23242510, Das et al (2013) cp437

Displaying a total number of 1 proband entries matching this variant.