ClinVar Miner

Submissions for variant NM_000222.2(KIT):c.1727T>C (p.Leu576Pro) (rs121913513)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000426330 SCV000504189 pathogenic Cutaneous melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433543 SCV000504190 likely pathogenic Gastrointestinal stroma tumor 2016-05-13 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443552 SCV000504191 pathogenic Thymoma 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426967 SCV000504192 not provided Non-small cell lung cancer 2016-03-10 no assertion provided literature only

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