ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4836G>T (p.Leu1612=)

dbSNP: rs1765779549
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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 RCV003774106 SCV002490312 likely benign Familial adenomatous polyposis 1 2022-10-17 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003774106 SCV004932720 benign Familial adenomatous polyposis 1 2024-03-28 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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