ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.180A>C (p.Pro60=) (rs749289195)

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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 RCV000165331 SCV000216054 likely benign Hereditary cancer-predisposing syndrome 2014-08-13 criteria provided, single submitter clinical testing
Color RCV000165331 SCV000691584 likely benign Hereditary cancer-predisposing syndrome 2017-03-31 criteria provided, single submitter clinical testing
Counsyl RCV000411950 SCV000489714 likely benign Li-Fraumeni syndrome 1 2016-11-11 criteria provided, single submitter clinical testing
Invitae RCV000200475 SCV000253306 likely benign Li-Fraumeni syndrome 2017-11-01 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506875 SCV000602263 likely benign not specified 2016-09-09 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759371 SCV000888661 likely benign not provided 2018-03-30 criteria provided, single submitter clinical testing

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