ClinVar Miner

Submissions for variant NM_001288705.3(CSF1R):c.2906A>T (p.Tyr969Phe)

dbSNP: rs1801271
Minimum review status: Collection method:
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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) RCV000439671 SCV000505554 likely pathogenic Hematologic neoplasm 2016-05-13 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419424 SCV000505555 likely pathogenic Neoplasm 2015-07-14 no assertion criteria provided literature only

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