ClinVar Miner

Submissions for variant NM_001198800.3(ASCC1):c.714C>A (p.Tyr238Ter)

dbSNP: rs138245920
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001706772 SCV001934252 pathogenic Barrett esophagus 2020-10-19 criteria provided, single submitter clinical testing

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