ClinVar Genomic variation as it relates to human health
NM_004364.5(CEBPA):c.405C>G (p.Ala135=)
Germline
Classification
(1)
Likely benign
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 | |||
CEBPA | No evidence available | No evidence available |
GRCh38 GRCh37 |
939 | 1009 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
CEBPA-related disorder
|
Likely benign (1) |
|
Apr 20, 2023 | RCV003983569.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 19, 2024