ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3971_3983dup (p.Ser1329fs)

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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. RCV003450223 SCV004185552 likely pathogenic Lynch syndrome 5 2023-08-28 criteria provided, single submitter clinical testing This variant is considered likely pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

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