ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.609G>T (p.Pro203=)

dbSNP: rs786201228
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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 RCV000930049 SCV001075691 likely benign Peutz-Jeghers syndrome 2024-03-16 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000930049 SCV006089113 benign Peutz-Jeghers syndrome 2025-03-26 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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