ClinVar Genomic variation as it relates to human health
NM_015267.4(CUX2):c.1606G>A (p.Ala536Thr)
Germline
Classification
(2)
Likely benign
criteria provided, multiple submitters, no conflicts
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 | |||
CUX2 | - | - |
GRCh38 GRCh37 |
264 | 273 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Nov 18, 2022 | RCV002968989.2 | |
Likely benign (1) |
|
Oct 1, 2022 | RCV003395669.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024