ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.1284_1285del (p.Lys429fs)

dbSNP: rs1893193729
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research RCV001201057 SCV001372063 pathogenic DICER1-related tumor predisposition 2019-07-01 criteria provided, single submitter curation ACMG criteria met: PVS1, PM2, PM7, PP4
CeGaT Center for Human Genetics Tuebingen RCV001310719 SCV001500628 pathogenic not provided 2021-02-01 criteria provided, single submitter clinical testing

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