ClinVar Miner

Submissions for variant NM_014780.4(CUL7):c.1027C>T (p.Pro343Ser) (rs113845886)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000347674 SCV000463422 likely benign Three M syndrome 2016-06-14 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000513793 SCV000609571 benign not provided 2017-02-23 criteria provided, single submitter clinical testing

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