ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2262T>C (p.Val754=) (rs148987776)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000547063 SCV000647228 likely benign Familial adenomatous polyposis 1 2017-03-29 criteria provided, single submitter clinical testing
Ambry Genetics RCV000568933 SCV000667234 likely benign Hereditary cancer-predisposing syndrome 2017-05-22 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000568933 SCV000686885 likely benign Hereditary cancer-predisposing syndrome 2017-08-30 criteria provided, single submitter clinical testing

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