ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3387G>A (p.Leu1129=)

dbSNP: rs730881225
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004440006 SCV004932478 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.
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005230622 SCV005876599 likely benign not provided 2023-12-08 criteria provided, single submitter clinical testing

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