ClinVar Miner

Submissions for variant NM_005188.3(CBL):c.1099_1101del (p.Gln367del) (rs1555230070)

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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 RCV000627092 SCV000747841 uncertain significance Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia 2018-05-15 criteria provided, single submitter clinical testing

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