ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7671C>G (p.Ser2557=)

dbSNP: rs1580685454
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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 RCV004562857 SCV001632360 likely benign Familial adenomatous polyposis 1 2021-10-25 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004562857 SCV005085181 benign Familial adenomatous polyposis 1 2024-04-10 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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