ClinVar Miner

List of variants in gene FLT3 studied for acute myeloid leukemia

Included ClinVar conditions (22):
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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_004119.2(FLT3):c.1715A>G (p.Tyr572Cys) rs121913491
NM_004119.2(FLT3):c.1736T>C (p.Val579Ala) rs1057520022
NM_004119.2(FLT3):c.1771T>G (p.Tyr591Asp) rs1057520043
NM_004119.2(FLT3):c.1772A>G (p.Tyr591Cys) rs1057520024
NM_004119.2(FLT3):c.1775T>C (p.Val592Ala) rs1057520025
NM_004119.2(FLT3):c.1780T>C (p.Phe594Leu) rs1057520021
NM_004119.2(FLT3):c.1855G>T (p.Gly619Cys) rs1057519769
NM_004119.2(FLT3):c.1952A>G (p.Asp651Gly) rs1057519768
NM_004119.2(FLT3):c.1987A>C (p.Lys663Gln) rs1057520026
NM_004119.2(FLT3):c.2026A>G (p.Asn676Asp) rs1057519767
NM_004119.2(FLT3):c.2028C>A (p.Asn676Lys) rs1057519766
NM_004119.2(FLT3):c.2028C>G (p.Asn676Lys) rs1057519766
NM_004119.2(FLT3):c.2059A>T (p.Ile687Phe) rs1057519765
NM_004119.2(FLT3):c.2073T>A (p.Phe691Leu) rs1057519764
NM_004119.2(FLT3):c.2073T>G (p.Phe691Leu) rs1057519764
NM_004119.2(FLT3):c.2211G>C (p.Met737Ile)
NM_004119.2(FLT3):c.2503G>A (p.Asp835Asn) rs121913488
NM_004119.2(FLT3):c.2503G>C (p.Asp835His) rs121913488
NM_004119.2(FLT3):c.2503G>T (p.Asp835Tyr) rs121913488
NM_004119.2(FLT3):c.2503_2504delinsTT (p.Asp835Phe) rs1057519763
NM_004119.2(FLT3):c.2503_2505del (p.Asp835del) rs121913486
NM_004119.2(FLT3):c.2504A>C (p.Asp835Ala) rs121909646
NM_004119.2(FLT3):c.2504A>T (p.Asp835Val) rs121909646
NM_004119.2(FLT3):c.2505T>A (p.Asp835Glu) rs121913487
NM_004119.2(FLT3):c.2505T>G (p.Asp835Glu) rs121913487
NM_004119.2(FLT3):c.2506A>C (p.Ile836Leu) rs1057519726
NM_004119.2(FLT3):c.2506A>G (p.Ile836Val) rs1057519726
NM_004119.2(FLT3):c.2506A>T (p.Ile836Phe) rs1057519726
NM_004119.2(FLT3):c.2507T>G (p.Ile836Ser) rs1057520023
NM_004119.2(FLT3):c.2508C>G (p.Ile836Met) rs121913232
NM_004119.2(FLT3):c.2508_2510del (p.Ile836del) rs121913490
NM_004119.2(FLT3):c.2516A>G (p.Asp839Gly) rs991132188
NM_004119.2(FLT3):c.2520_2521insGGATCC (p.Asn841_Tyr842insGlySer) rs398122514
NM_004119.2(FLT3):c.2521A>C (p.Asn841His) rs772061268
NM_004119.2(FLT3):c.2523C>A (p.Asn841Lys) rs749281035
NM_004119.2(FLT3):c.2524T>C (p.Tyr842His) rs1057519762
NM_004119.2(FLT3):c.2525A>G (p.Tyr842Cys) rs376588714

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