ClinVar Miner

Submissions for variant NM_052988.5(CDK10):c.503del (p.Asn168fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Medical Genetics (UMR_S 1112), INSERM/Strasbourg University RCV003329156 SCV004035939 pathogenic Al Kaissi syndrome criteria provided, single submitter clinical testing

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