ClinVar Miner

Submissions for variant NM_003588.3(CUL4B):c.2577G>C (p.Lys859Asn) (rs1556181426)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology RCV000515477 SCV000611593 uncertain significance Syndromic X-linked mental retardation, Cabezas type 2017-09-14 criteria provided, single submitter research

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