ClinVar Miner

Submissions for variant NM_000038.6(APC):c.5808A>G (p.Ser1936=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004589466 SCV005085754 benign Familial adenomatous polyposis 1 2024-04-02 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV004589466 SCV005832806 likely benign Familial adenomatous polyposis 1 2024-02-14 criteria provided, single submitter clinical testing

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