ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.87C>T (p.Ile29=)

dbSNP: rs745530022
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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 RCV001444694 SCV001647704 likely benign Peutz-Jeghers syndrome 2020-03-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001444694 SCV006096157 benign Peutz-Jeghers syndrome 2025-03-24 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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