ClinVar Miner

Submissions for variant NM_001211.5(BUB1B):c.2208_2211dup (p.Ser738Valfs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000007158 SCV000027354 pathogenic Mosaic variegated aneuploidy syndrome 1 2004-11-01 no assertion criteria provided literature only
OMIM RCV000007159 SCV000027355 affects Premature chromatid separation trait 2004-11-01 no assertion criteria provided literature only

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