ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2656_2668delinsTCTAAA (p.Ile886fs) (rs1114167703)

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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 RCV000491891 SCV000580135 pathogenic Hereditary cancer-predisposing syndrome 2015-01-20 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Other acmg-defined mutation (i.e. initiation codon or gross deletion)

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