ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.2604T>C (p.Thr868=) (rs1428997179)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503666 SCV000591814 likely benign not specified 2015-06-03 criteria provided, single submitter clinical testing
Color RCV000776710 SCV000912339 likely benign Hereditary cancer-predisposing syndrome 2018-07-03 criteria provided, single submitter clinical testing
Ambry Genetics RCV000776710 SCV001176948 likely benign Hereditary cancer-predisposing syndrome 2019-08-07 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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