ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2061C>G (p.Leu687=)

dbSNP: rs2149859680
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004440386 SCV004932841 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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