ClinVar Miner

List of variants in gene FLNB reported as uncertain significance for bone disorder

Included ClinVar conditions (1436):
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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.808A>G (p.Met270Val) rs145036794 0.00096
NM_001457.4(FLNB):c.4730C>T (p.Ala1577Val) rs148101195 0.00043
NM_001457.4(FLNB):c.1588G>T (p.Gly530Trp) rs773943113 0.00022
NM_001457.4(FLNB):c.7036C>T (p.Arg2346Cys) rs149638325 0.00014
NM_001457.4(FLNB):c.6028C>T (p.Arg2010Cys) rs138034708 0.00013
NM_001457.4(FLNB):c.572C>T (p.Pro191Leu) rs368472521 0.00004
NM_001457.4(FLNB):c.5917G>A (p.Glu1973Lys) rs368965386 0.00004
NM_001457.4(FLNB):c.6164G>A (p.Gly2055Asp) rs375752014 0.00004
NM_001457.4(FLNB):c.906+3A>G rs750429255 0.00004
NM_001457.4(FLNB):c.1298C>A (p.Ala433Asp) rs1455523738 0.00003
NM_001457.4(FLNB):c.3325G>A (p.Val1109Ile) rs200947960 0.00003
NM_001457.4(FLNB):c.3724+4G>C rs993620203 0.00003
NM_001457.4(FLNB):c.4813C>T (p.Arg1605Cys) rs745461413 0.00003
NM_001457.4(FLNB):c.7723G>A (p.Val2575Ile) rs369949841 0.00003
NM_001457.4(FLNB):c.776C>T (p.Ala259Val) rs376619286 0.00003
NM_001457.4(FLNB):c.4585T>C (p.Ser1529Pro) rs770433500 0.00002
NM_001457.4(FLNB):c.2195A>G (p.Tyr732Cys) rs1266538760 0.00001
NM_001457.4(FLNB):c.2892C>G (p.Phe964Leu) rs779195648 0.00001
NM_001457.4(FLNB):c.3064G>A (p.Gly1022Arg) rs1057005655 0.00001
NM_001457.4(FLNB):c.3350A>G (p.His1117Arg) rs779765790 0.00001
NM_001457.4(FLNB):c.3616A>G (p.Met1206Val) rs756396172 0.00001
NM_001457.4(FLNB):c.4313G>A (p.Arg1438His) rs199590811 0.00001
NM_001457.4(FLNB):c.4520T>C (p.Phe1507Ser) rs765086454 0.00001
NM_001457.4(FLNB):c.4589A>G (p.Tyr1530Cys) rs776043627 0.00001
NM_001457.4(FLNB):c.4826C>T (p.Thr1609Ile) rs761698437 0.00001
NM_001457.4(FLNB):c.5059T>C (p.Tyr1687His) rs774862180 0.00001
NM_001457.4(FLNB):c.928G>A (p.Asp310Asn) rs1576709484 0.00001
NM_001457.4(FLNB):c.1153G>C (p.Gly385Arg)
NM_001457.4(FLNB):c.1346-2A>G rs757004353
NM_001457.4(FLNB):c.1626A>T (p.Gln542His)
NM_001457.4(FLNB):c.1652A>T (p.Lys551Ile)
NM_001457.4(FLNB):c.1864T>C (p.Cys622Arg) rs2471077153
NM_001457.4(FLNB):c.1887C>G (p.Asp629Glu) rs377324244
NM_001457.4(FLNB):c.199C>T (p.His67Tyr) rs751371914
NM_001457.4(FLNB):c.2138C>A (p.Ala713Asp)
NM_001457.4(FLNB):c.2158G>A (p.Val720Met)
NM_001457.4(FLNB):c.2417C>A (p.Thr806Lys) rs940585956
NM_001457.4(FLNB):c.2471T>C (p.Leu824Pro) rs2107121791
NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys) rs139875974
NM_001457.4(FLNB):c.2932G>A (p.Asp978Asn)
NM_001457.4(FLNB):c.2996G>A (p.Arg999Gln) rs755928543
NM_001457.4(FLNB):c.3083G>A (p.Ser1028Asn)
NM_001457.4(FLNB):c.3173C>T (p.Pro1058Leu) rs1274949470
NM_001457.4(FLNB):c.3239C>T (p.Pro1080Leu)
NM_001457.4(FLNB):c.4229C>G (p.Pro1410Arg) rs2107204256
NM_001457.4(FLNB):c.4391G>C (p.Gly1464Ala) rs886044175
NM_001457.4(FLNB):c.4419C>A (p.Asp1473Glu)
NM_001457.4(FLNB):c.4427A>G (p.Asp1476Gly) rs2471154590
NM_001457.4(FLNB):c.4570G>C (p.Gly1524Arg) rs2107220190
NM_001457.4(FLNB):c.4805C>A (p.Ser1602Tyr) rs2107224888
NM_001457.4(FLNB):c.4967A>T (p.Asp1656Val) rs201848913
NM_001457.4(FLNB):c.501C>A (p.Asp167Glu) rs746892435
NM_001457.4(FLNB):c.5081A>G (p.Asp1694Gly)
NM_001457.4(FLNB):c.545T>G (p.Leu182Arg) rs2470996279
NM_001457.4(FLNB):c.5524T>C (p.Phe1842Leu) rs1178860596
NM_001457.4(FLNB):c.5696T>A (p.Ile1899Asn) rs2471200222
NM_001457.4(FLNB):c.592G>A (p.Ala198Thr)
NM_001457.4(FLNB):c.6073G>A (p.Val2025Met)
NM_001457.4(FLNB):c.6643A>G (p.Ser2215Gly) rs2097350829
NM_001457.4(FLNB):c.6866G>A (p.Arg2289His) rs1033252725
NM_001457.4(FLNB):c.6994G>A (p.Glu2332Lys) rs139262140
NM_001457.4(FLNB):c.7328C>G (p.Thr2443Ser)
NM_001457.4(FLNB):c.7351C>G (p.Leu2451Val) rs2107340030
NM_001457.4(FLNB):c.7624T>C (p.Ser2542Pro) rs2097380898
NM_001457.4(FLNB):c.7760G>T (p.Trp2587Leu) rs144321868
NM_001457.4(FLNB):c.871G>A (p.Val291Met) rs751747906

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