ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4011G>T (p.Leu1337=)

dbSNP: rs1765579898
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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 RCV004565218 SCV002399211 likely benign Familial adenomatous polyposis 1 2022-06-14 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004565218 SCV004933662 benign Familial adenomatous polyposis 1 2024-03-25 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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