ClinVar Miner

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

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_182925.5(FLT4):c.1104-42T>C rs402647 0.94231
NM_182925.5(FLT4):c.3220-29A>G rs659268 0.76189
NM_182925.5(FLT4):c.2761+44G>A rs446003 0.66129
NM_182925.5(FLT4):c.2670C>G (p.His890Gln) rs448012 0.61446
NM_182925.5(FLT4):c.1103+18C>T rs438464 0.48279
NM_182925.5(FLT4):c.986-45C>T rs13359473 0.27306
NM_182925.5(FLT4):c.3198C>T (p.Pro1066=) rs1130378 0.24024
NM_182925.5(FLT4):c.2168-49G>A rs2242214 0.23522
NM_182925.5(FLT4):c.401-19G>C rs56188706 0.13320
NM_182925.5(FLT4):c.445A>G (p.Asn149Asp) rs34221241 0.07968
NM_182925.5(FLT4):c.3437G>A (p.Arg1146His) rs1130379 0.07352
NM_182925.5(FLT4):c.507G>T (p.Leu169=) rs3736061 0.06624
NM_182925.5(FLT4):c.1103+33A>C rs75361132 0.05432
NM_182925.5(FLT4):c.2168-28A>G rs2242215 0.05387
NM_182925.5(FLT4):c.3807+34G>C rs2242219 0.05136
NM_182925.5(FLT4):c.1258+14G>A rs56193546 0.04092
NM_182925.5(FLT4):c.1258+21C>T rs56401579 0.03787
NM_182925.5(FLT4):c.677-28G>A rs56361806 0.03133
NM_182925.5(FLT4):c.489C>T (p.Pro163=) rs75516704 0.02840
NM_182925.5(FLT4):c.1580A>G (p.Asn527Ser) rs35874891 0.02531
NM_182925.5(FLT4):c.3959G>A (p.Arg1320Gln) rs115824945 0.02490
NM_182925.5(FLT4):c.1344C>T (p.Tyr448=) rs3736062 0.02437
NM_182925.5(FLT4):c.633A>G (p.Gly211=) rs34117331 0.02393
NM_182925.5(FLT4):c.400+17G>A rs59410886 0.01755
NM_182925.5(FLT4):c.3147C>T (p.Asp1049=) rs56127961 0.01268
NM_182925.5(FLT4):c.76T>G (p.Ser26Ala) rs113995355 0.00708
NM_182925.5(FLT4):c.3002-18C>A rs113793749 0.00620
NM_182925.5(FLT4):c.1049A>T (p.Glu350Val) rs111916034 0.00432
NM_182925.5(FLT4):c.1921C>T (p.Pro641Ser) rs55667289 0.00349
NM_182925.5(FLT4):c.2860C>T (p.Pro954Ser) rs34255532 0.00275
NM_182925.5(FLT4):c.3908G>C (p.Gly1303Ala) rs146806202 0.00227
NM_182925.5(FLT4):c.3681C>T (p.Ala1227=) rs140710164 0.00218
NM_182925.5(FLT4):c.1038G>A (p.Thr346=) rs201326194 0.00016
NM_182925.5(FLT4):c.1103+20A>C rs383985
NM_182925.5(FLT4):c.1103+20A>G rs383985
NM_182925.5(FLT4):c.1421+19_1421+37del rs144453562
NM_182925.5(FLT4):c.1480A>G (p.Thr494Ala) rs307826
NM_182925.5(FLT4):c.3219+37G>C rs55657009
NM_182925.5(FLT4):c.3971G>T (p.Arg1324Leu) rs307821

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