ClinVar Miner

Submissions for variant NM_000222.2(KIT):c.1669T>A (p.Trp557Arg) (rs121913235)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000421211 SCV000504166 pathogenic Cutaneous melanoma 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431900 SCV000504167 likely pathogenic Gastrointestinal stroma tumor 2016-05-13 no assertion criteria provided literature only

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