ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4971G>C (p.Leu1657=)

dbSNP: rs786202058
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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) RCV000495128 SCV000578272 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2017-06-29 reviewed by expert panel curation Synonymous substitution variant, with low bioinformatic likelihood to result in a splicing aberration (Splicing prior probability 0.02; http://priors.hci.utah.edu/PRIORS/).
Ambry Genetics RCV000570845 SCV000665912 likely benign Hereditary cancer-predisposing syndrome 2017-03-13 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Invitae RCV001467065 SCV001671082 likely benign Hereditary breast ovarian cancer syndrome 2022-07-20 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV000495128 SCV001238363 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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