ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2538T>A (p.Ser846=) (rs759201675)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000541407 SCV000647242 likely benign Familial adenomatous polyposis 1 2017-05-17 criteria provided, single submitter clinical testing
Ambry Genetics RCV000562201 SCV000667768 likely benign Hereditary cancer-predisposing syndrome 2017-07-03 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence,Synonymous alterations with insufficient evidence to classify as benign

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