ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.1152G>A (p.Arg384=)

dbSNP: rs786201491
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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 RCV003049426 SCV003341542 likely benign Peutz-Jeghers syndrome 2022-07-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003049426 SCV006091300 benign Peutz-Jeghers syndrome 2025-03-28 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.

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