ClinVar Miner

Submissions for variant NM_000222.2(KIT):c.1674G>T (p.Lys558Asn) (rs200375589)

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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) RCV000426003 SCV000504172 likely pathogenic Gastrointestinal stroma tumor 2016-05-13 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436617 SCV000504173 pathogenic Cutaneous melanoma 2014-10-02 no assertion criteria provided literature only

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