ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3588A>C (p.Ser1196=)

dbSNP: rs1765463829
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV004037388 SCV001702845 likely benign Familial adenomatous polyposis 1 2019-01-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004037388 SCV004931485 benign Familial adenomatous polyposis 1 2024-03-21 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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