ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1059G>A (p.Lys353=)

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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. RCV005246219 SCV005894980 benign Lynch syndrome 1 2024-12-06 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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