ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.10G>A (p.Val4Met) (rs767300470)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000563171 SCV000664342 uncertain significance Hereditary cancer-predisposing syndrome 2016-01-22 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Co-occurence with a mutation in another gene that clearly explains a proband's phenotype,In silico models in agreement (benign),Insufficient or conflicting evidence

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