ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2613A>C (p.Gly871=) (rs36046448)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000197250 SCV000252912 likely benign Familial adenomatous polyposis 1 2017-05-09 criteria provided, single submitter clinical testing
Ambry Genetics RCV000570142 SCV000667257 likely benign Hereditary cancer-predisposing syndrome 2016-09-28 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: In silico models in agreement (benign),Synonymous alterations with insufficient evidence to classify as benign
Color RCV000570142 SCV000681540 likely benign Hereditary cancer-predisposing syndrome 2016-12-13 criteria provided, single submitter clinical testing

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