ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.608dup (p.Phe204fs) (rs1131690946)

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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 RCV000492160 SCV000580936 pathogenic Hereditary cancer-predisposing syndrome 2014-04-15 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Alterations resulting in premature truncation (e.g.reading frame shift, nonsense)

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