ClinVar Miner

Submissions for variant NM_000038.6(APC):c.6112C>T (p.Leu2038=)

dbSNP: rs1433119360
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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 RCV004572061 SCV002425821 likely benign Familial adenomatous polyposis 1 2023-10-29 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004572061 SCV005083807 benign Familial adenomatous polyposis 1 2024-04-03 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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