ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.924G>C (p.Leu308=) (rs786202546)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000575062 SCV000664390 likely benign Hereditary cancer-predisposing syndrome 2015-11-27 criteria provided, single submitter clinical testing
Color RCV000575062 SCV000691665 likely benign Hereditary cancer-predisposing syndrome 2017-10-12 criteria provided, single submitter clinical testing
Invitae RCV000462950 SCV000557350 likely benign Li-Fraumeni syndrome 2016-09-21 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506600 SCV000602283 uncertain significance not specified 2016-10-29 criteria provided, single submitter clinical testing

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