ClinVar Genomic variation as it relates to human health
NM_000075.4(CDK4):c.889_903del (p.Lys297_Asn301del)
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
CDK4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
559 | 1067 | |
TSPAN31 | - | - |
GRCh38 GRCh37 |
9 | 414 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 9, 2022 | RCV003059731.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 29, 2024