ClinVar Miner

Submissions for variant NM_004119.2(FLT3):c.2503_2505del (p.Asp835del) (rs121913486)

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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) RCV000017667 SCV000505671 likely pathogenic Acute myeloid leukemia 2015-07-14 no assertion criteria provided literature only
OMIM RCV000017667 SCV000037944 pathogenic Acute myeloid leukemia 2001-06-01 no assertion criteria provided literature only

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