ClinVar Miner

Submissions for variant NM_001079872.2(CUL4B):c.986T>C (p.Ile329Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289154 SCV002578958 uncertain significance X-linked intellectual disability Cabezas type 2022-04-25 criteria provided, single submitter clinical testing

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