ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1676_1720del (p.Val559_Thr574delinsAla)

dbSNP: rs1560417535
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular Diagnostics, Institute of Oncology Ljubljana RCV000771012 SCV000902500 likely pathogenic Gastrointestinal stromal tumor 2019-05-15 criteria provided, single submitter clinical testing

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