ClinVar Genomic variation as it relates to human health
NM_000059.4(BRCA2):c.10023C>T (p.Asp3341=)
Germline
Top reviewed classifications are shown here.
Submission summary:
Reviewed by expert panel
Likely benign
Jun 2017 by
Evidence-based…
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 | |||
BRCA2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
18967 | 19126 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (2) |
|
Dec 18, 2017 | RCV000164212.6 | |
Likely benign (2) |
|
Jun 29, 2017 | RCV000495017.4 | |
Benign/Likely benign (5) |
|
Apr 1, 2024 | RCV000759569.16 | |
Benign/Likely benign (2) |
|
Jan 3, 2024 | RCV001079160.6 | |
Likely benign (1) |
|
Apr 22, 2019 | RCV001194385.1 |
Citations for germline classification of this variant
HelpText-mined citations for rs113507014 ...
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 Oct 20, 2024