ClinVar Miner

Submissions for variant NM_000222.2(KIT):c.2466T>G (p.Asn822Lys) (rs121913514)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000419001 SCV000504220 likely pathogenic Gastrointestinal stroma tumor 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429190 SCV000504221 pathogenic Cutaneous melanoma 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439434 SCV000504222 likely pathogenic Acute myeloid leukemia 2014-12-26 no assertion criteria provided literature only

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