ClinVar Miner

Submissions for variant NM_001759.4(CCND2):c.829C>T (p.Gln277Ter)

dbSNP: rs1864225645
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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 Medical Genetics and Applied Genomics, University Hospital Tübingen RCV001268523 SCV001447508 likely pathogenic not provided 2020-10-23 criteria provided, single submitter clinical testing

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