ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2812del (p.Asp938fs) (rs1114167757)

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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 RCV000491193 SCV000580285 pathogenic Hereditary cancer-predisposing syndrome 2016-06-30 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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