ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.2334C>T (p.Gly778=)

gnomAD frequency: 0.00002  dbSNP: rs777404687
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Total submissions: 5
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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) RCV000495363 SCV000578433 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/).
Color Diagnostics, LLC DBA Color Health RCV000583616 SCV000688379 likely benign Hereditary cancer-predisposing syndrome 2016-06-13 criteria provided, single submitter clinical testing
Invitae RCV000703144 SCV000832029 likely benign Hereditary breast ovarian cancer syndrome 2023-09-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV000583616 SCV002732518 likely benign Hereditary cancer-predisposing syndrome 2022-07-25 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: 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.
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002509412 SCV002819932 likely benign not specified 2022-12-31 criteria provided, single submitter clinical testing

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