ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.458C>T (p.Ala153Val) (rs1555737824)

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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 RCV000565289 SCV000672317 uncertain significance Hereditary cancer-predisposing syndrome 2016-11-07 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: In silico models in agreement (deleterious) and/or completely conserved position in appropriate species,Insufficient evidence

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