ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8308del (p.Ala2770fs) (rs398122601)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) RCV000077023 SCV000301261 pathogenic Breast-ovarian cancer, familial 2 2016-09-08 reviewed by expert panel curation Variant allele predicted to encode a truncated non-functional protein.
Ambry Genetics RCV000216064 SCV000277088 pathogenic Hereditary cancer-predisposing syndrome 2015-07-15 criteria provided, single submitter clinical testing
Invitae RCV000809840 SCV000950019 pathogenic Hereditary breast and ovarian cancer syndrome 2018-11-21 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ala2770Profs*7) in the BRCA2 gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This variant has been reported in individuals in the Leiden Open-source Variation Database (PMID: 21520333). ClinVar contains an entry for this variant (Variation ID: 91506). Loss-of-function variants in BRCA2 are known to be pathogenic (PMID: 20104584). For these reasons, this variant has been classified as Pathogenic.
Sharing Clinical Reports Project (SCRP) RCV000077023 SCV000108820 pathogenic Breast-ovarian cancer, familial 2 2009-11-30 no assertion criteria provided clinical testing

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