ClinVar Genomic variation as it relates to human health
NM_000626.4(CD79B):c.523G>A (p.Val175Met)
Germline
Classification
(2)
Uncertain significance
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 | |||
CD79B | - | - |
GRCh38 GRCh37 |
- | 180 | |
GH-LCR | - | - | - | GRCh38 | - | 1611 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 14, 2022 | RCV003092805.2 | |
CD79B-related disorder
|
Uncertain significance (1) |
|
Feb 28, 2023 | RCV003420337.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 27, 2024