ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.84G>T (p.Pro28=)

dbSNP: rs746695035
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002102288 SCV002327213 likely benign Familial cancer of breast 2021-08-04 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002102288 SCV005403333 benign Familial cancer of breast 2024-07-18 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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