List of variants reported as likely pathogenic for Hematologic neoplasm by Database of Curated Mutations (DoCM)

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005188.4(CBL):c.1111T>C (p.Tyr371His)	rs267606706	0.00001
NM_005373.3(MPL):c.1544G>T (p.Trp515Leu)	rs121913615	0.00001
NM_000222.3(KIT):c.1924A>G (p.Lys642Glu)	rs121913512
NM_000222.3(KIT):c.2446G>C (p.Asp816His)	rs121913506
NM_000222.3(KIT):c.2446G>T (p.Asp816Tyr)	rs121913506
NM_000222.3(KIT):c.2447A>T (p.Asp816Val)	rs121913507
NM_001288705.3(CSF1R):c.1711T>G (p.Tyr571Asp)	rs1057519802
NM_001288705.3(CSF1R):c.2905T>C (p.Tyr969His)	rs121913393
NM_001288705.3(CSF1R):c.2906A>G (p.Tyr969Cys)	rs1801271
NM_001288705.3(CSF1R):c.2906A>T (p.Tyr969Phe)	rs1801271
NM_001288705.3(CSF1R):c.902T>C (p.Leu301Ser)	rs121913390
NM_001288705.3(CSF1R):c.903G>T (p.Leu301Phe)	rs1057520014
NM_005188.4(CBL):c.1150T>C (p.Cys384Arg)	rs387906664

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