ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.2149G>T (p.Gly717Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003140873 SCV003818945 uncertain significance MHC class I deficiency 2019-10-16 criteria provided, single submitter clinical testing

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