ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3776A>C (p.Asn1259Thr) (rs1258636828)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000572547 SCV000662427 uncertain significance Hereditary cancer-predisposing syndrome 2016-11-16 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence,In silico models in agreement (benign)
Color RCV000572547 SCV000913112 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-19 criteria provided, single submitter clinical testing

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