ClinVar Miner

List of variants in gene FLT4 reported as likely benign for not specified

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_182925.5(FLT4):c.58+28C>G rs147801168 0.02861
NM_182925.5(FLT4):c.1421+37C>T rs201306288 0.01418
NM_182925.5(FLT4):c.401-34G>A rs77918653 0.01278
NM_182925.5(FLT4):c.59-24C>T rs138954560 0.01077
NM_182925.5(FLT4):c.3962G>A (p.Arg1321Gln) rs79620092 0.00954
NM_182925.5(FLT4):c.3001+31T>G rs201575824 0.00469
NM_182925.5(FLT4):c.1422-10G>A rs199699017 0.00389
NM_182925.5(FLT4):c.1921C>T (p.Pro641Ser) rs55667289 0.00349
NM_182925.5(FLT4):c.3220-21A>C rs2934601 0.00231
NM_182925.5(FLT4):c.1658-17T>G rs113217491 0.00150
NM_182925.5(FLT4):c.3220-11T>C rs2934602 0.00068
NM_182925.5(FLT4):c.2543-14C>T rs200117836 0.00045
NM_182925.5(FLT4):c.1308G>A (p.Ser436=) rs142130840 0.00039
NM_182925.5(FLT4):c.234G>A (p.Thr78=) rs144964143 0.00029
NM_182925.5(FLT4):c.3220-10G>T rs369575233 0.00022
NM_182925.5(FLT4):c.3537+21G>A rs377256001 0.00021
NM_182925.5(FLT4):c.676+18C>T rs367885321 0.00019
NM_182925.5(FLT4):c.1815G>A (p.Pro605=) rs368166608 0.00008
NM_182925.5(FLT4):c.475C>G (p.Leu159Val) rs147634448 0.00008
NM_182925.5(FLT4):c.2648-8C>T rs752689922 0.00006
NM_182925.5(FLT4):c.4005C>T (p.Ser1335=) rs774068221 0.00006
NM_182925.5(FLT4):c.816+18G>C rs761356839 0.00004
NM_182925.5(FLT4):c.3971G>C (p.Arg1324Pro) rs307821
NM_182925.5(FLT4):c.677-15T>C rs886038755

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