ClinVar Miner

List of variants in gene FLT4 studied for cardiovascular disorder

Included ClinVar conditions (1435):
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Gene type:
ClinVar version:
Total variants: 34
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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.3198C>T (p.Pro1066=) rs1130378 0.24024
NM_182925.5(FLT4):c.2168-49G>A rs2242214 0.23522
NM_182925.5(FLT4):c.2860C>T (p.Pro954Ser) rs34255532 0.00275
NM_182925.5(FLT4):c.2563G>A (p.Ala855Thr) rs121909657 0.00009
NM_182925.5(FLT4):c.1093G>A (p.Glu365Lys) rs369919880 0.00007
NM_182925.5(FLT4):c.1103+20A>C rs383985
NM_182925.5(FLT4):c.1104-2A>G
NM_182925.5(FLT4):c.1519T>C (p.Trp507Arg)
NM_182925.5(FLT4):c.2569G>A (p.Gly857Arg) rs267606818
NM_182925.5(FLT4):c.2632G>A (p.Val878Met) rs121909654
NM_182925.5(FLT4):c.2717_2734dup (p.Asn911_Leu912insHisLeuAsnValValAsn)
NM_182925.5(FLT4):c.2771T>A (p.Met924Lys)
NM_182925.5(FLT4):c.3023C>T (p.Pro1008Leu) rs149033942
NM_182925.5(FLT4):c.3104A>G (p.His1035Arg) rs121909653
NM_182925.5(FLT4):c.3109G>A (p.Asp1037Asn)
NM_182925.5(FLT4):c.3121C>T (p.Arg1041Trp) rs1451816005
NM_182925.5(FLT4):c.3122G>A (p.Arg1041Gln)
NM_182925.5(FLT4):c.3122G>C (p.Arg1041Pro) rs121909650
NM_182925.5(FLT4):c.3131T>C (p.Leu1044Pro) rs121909651
NM_182925.5(FLT4):c.3179G>A (p.Arg1060Gln)
NM_182925.5(FLT4):c.3247C>T (p.Pro1083Ser) rs1762428823
NM_182925.5(FLT4):c.3257T>C (p.Ile1086Thr) rs121909655
NM_182925.5(FLT4):c.3316G>A (p.Glu1106Lys) rs121909656
NM_182925.5(FLT4):c.3320TCT[1] (p.Phe1108del) rs587776833
NM_182925.5(FLT4):c.3332G>A (p.Gly1111Glu)
NM_182925.5(FLT4):c.3341C>T (p.Pro1114Leu) rs121909652
NM_182925.5(FLT4):c.3410C>T (p.Pro1137Leu) rs1762335528
NM_182925.5(FLT4):c.3610A>G (p.Thr1204Ala) rs1189576922
NM_182925.5(FLT4):c.3821A>T (p.Asp1274Val) rs1761973773

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