ClinVar Genomic variation as it relates to human health
NM_001323289.2(CDKL5):c.1296_1298del (p.Lys432_Tyr433delinsAsn)
Germline
Top reviewed classifications are shown here.
Submission summary:
Reviewed by expert panel
Uncertain significance
for
CDKL5 disorder
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
CDKL5 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1201 | 1965 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 12, 2015 | RCV000504427.6 | |
Uncertain significance (1) |
|
Mar 26, 2021 | RCV001507063.4 | |
Uncertain significance (1) |
|
May 31, 2022 | RCV002524164.2 |
Citations for germline classification of this variant
HelpText-mined citations for rs1555951997 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Aug 04, 2024