ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.650C>T (p.Pro217Leu) (rs587782146)

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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 RCV000130710 SCV000185597 uncertain significance Hereditary cancer-predisposing syndrome 2013-12-09 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
Color RCV000130710 SCV000910043 uncertain significance Hereditary cancer-predisposing syndrome 2018-04-24 criteria provided, single submitter clinical testing

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