ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.454_466del (p.Pro152fs) (rs876659215)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000220919 SCV000275423 pathogenic Hereditary cancer-predisposing syndrome 2015-04-17 criteria provided, single submitter clinical testing
German Consortium for Hereditary Breast and Ovarian Cancer Center Cologne,University Hospital Cologne RCV000785289 SCV000923857 pathogenic Ovarian Neoplasms 2018-12-01 no assertion criteria provided research

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