ClinVar Miner

Submissions for variant NM_016284.5(CNOT1):c.3398A>G (p.Tyr1133Cys)

dbSNP: rs2151928424
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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 Goettingen RCV001528180 SCV001739434 uncertain significance Vissers-Bodmer syndrome 2021-07-01 no assertion criteria provided clinical testing

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