ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.672+1G>T (rs863224499)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000776760 SCV000912404 likely pathogenic Hereditary cancer-predisposing syndrome 2018-05-09 criteria provided, single submitter clinical testing
German Consortium for Hereditary Breast and Ovarian Cancer Center Cologne,University Hospital Cologne RCV000785529 SCV000924101 likely pathogenic Ovarian Neoplasms 2018-12-01 no assertion criteria provided research
MutSpliceDB: a database of splice sites variants effects on splicing,NIH RCV000786829 SCV000925723 not provided not provided no assertion provided in vitro

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