List of variants in gene FLT3 reported as pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
FLT3, INTERNAL TANDEM DUP
NM_004119.3(FLT3):c.1777_1779del (p.Asp593del)	rs587776834
NM_004119.3(FLT3):c.2503G>A (p.Asp835Asn)	rs121913488
NM_004119.3(FLT3):c.2503G>C (p.Asp835His)	rs121913488
NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr)	rs121913488
NM_004119.3(FLT3):c.2503_2505del (p.Asp835del)	rs121913486
NM_004119.3(FLT3):c.2504A>C (p.Asp835Ala)	rs121909646
NM_004119.3(FLT3):c.2504A>T (p.Asp835Val)	rs121909646
NM_004119.3(FLT3):c.2505T>A (p.Asp835Glu)	rs121913487
NM_004119.3(FLT3):c.2505T>G (p.Asp835Glu)	rs121913487
NM_004119.3(FLT3):c.2506A>C (p.Ile836Leu)	rs1057519726
NM_004119.3(FLT3):c.2508C>G (p.Ile836Met)	rs121913232
NM_004119.3(FLT3):c.2520_2521insGGATCC (p.Ser840_Asn841insGlySer)	rs398122514

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