ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.920-5C>T (rs34361146)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000164926 SCV000215614 likely benign Hereditary cancer-predisposing syndrome 2019-02-28 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
Invitae RCV001087552 SCV000557372 likely benign Li-Fraumeni syndrome 2020-10-26 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000587880 SCV000697456 likely benign not provided 2016-03-07 criteria provided, single submitter clinical testing
Color Health, Inc RCV000164926 SCV000902814 likely benign Hereditary cancer-predisposing syndrome 2016-08-08 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000587880 SCV001151191 uncertain significance not provided 2018-04-01 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001283870 SCV001469328 benign not specified 2019-12-20 criteria provided, single submitter clinical testing

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