ClinVar Miner

Submissions for variant NM_001375524.1(TRRAP):c.3904G>A (p.Ala1302Thr)

dbSNP: rs1790410600
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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 Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV001171573 SCV001334365 uncertain significance not provided 2019-05-14 criteria provided, single submitter clinical testing

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