ClinVar Miner

Submissions for variant NM_177438.2(DICER1):c.1440T>C (p.Thr480=) (rs1555373201)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000570232 SCV000661994 likely benign Hereditary cancer-predisposing syndrome 2017-06-20 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Intronic alteration with no splicing impact by rt-pcr analysis or other splicing assay

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