ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3258C>A (p.Pro1086=) (rs863224331)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000459191 SCV000561521 likely benign Hereditary nonpolyposis colon cancer 2017-08-27 criteria provided, single submitter clinical testing
Ambry Genetics RCV000564931 SCV000662457 likely benign Hereditary cancer-predisposing syndrome 2016-03-31 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000564931 SCV000685375 likely benign Hereditary cancer-predisposing syndrome 2015-06-09 criteria provided, single submitter clinical testing

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