ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7875T>C (p.Ser2625=)

dbSNP: rs2149995309
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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. RCV004589431 SCV005085609 benign Familial adenomatous polyposis 1 2024-04-11 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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