ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1992T>G (p.Thr664=)

dbSNP: rs2149858311
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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 RCV004563934 SCV001634778 likely benign Familial adenomatous polyposis 1 2023-07-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004563934 SCV004933333 benign Familial adenomatous polyposis 1 2024-03-08 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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