ClinVar Miner

List of variants in gene FLNB studied for bone disorder

Included ClinVar conditions (1350):
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Gene type:
ClinVar version:
Total variants: 114
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.292+8C>A rs9831243 0.01775
NM_001457.4(FLNB):c.6017A>G (p.Lys2006Arg) rs62621996 0.00994
NM_001457.4(FLNB):c.1919C>T (p.Thr640Met) rs62621999 0.00943
NM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr) rs116826041 0.00739
NM_001457.4(FLNB):c.5426-10G>A rs183917041 0.00264
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.3583G>A (p.Val1195Met) rs200993986 0.00021
NM_001457.4(FLNB):c.5407A>T (p.Met1803Leu) rs200677473 0.00021
NM_001457.4(FLNB):c.4986C>T (p.Ala1662=) rs200905679 0.00017
NM_001457.4(FLNB):c.6028C>T (p.Arg2010Cys) rs138034708 0.00013
NM_001457.4(FLNB):c.1693G>A (p.Gly565Arg) rs754869116 0.00006
NM_001457.4(FLNB):c.572C>T (p.Pro191Leu) rs368472521 0.00005
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.3724+4G>C rs993620203 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.3325G>A (p.Val1109Ile) rs200947960 0.00002
NM_001457.4(FLNB):c.1243C>T (p.Arg415Ter) rs775714153 0.00001
NM_001457.4(FLNB):c.2452C>T (p.Arg818Ter) rs80356519 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.4819C>T (p.Arg1607Ter) rs80356520 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.871G>A (p.Val291Met) rs751747906 0.00001
NM_001457.4(FLNB):c.1081G>A (p.Gly361Ser) rs80356509
NM_001457.4(FLNB):c.1082G>A (p.Gly361Asp) rs794727854
NM_001457.4(FLNB):c.1088G>A (p.Gly363Glu) rs80356510
NM_001457.4(FLNB):c.1204del (p.Val402fs) rs2107062364
NM_001457.4(FLNB):c.1346-1358_1941+403del
NM_001457.4(FLNB):c.1346-2A>G rs757004353
NM_001457.4(FLNB):c.1429delinsCT (p.Val477fs) rs2107082636
NM_001457.4(FLNB):c.1493del (p.Glu498fs) rs2107092260
NM_001457.4(FLNB):c.1592dup (p.His532fs) rs746105983
NM_001457.4(FLNB):c.1739G>T (p.Gly580Val) rs2097257677
NM_001457.4(FLNB):c.1945C>T (p.Arg649Ter) rs80356517
NM_001457.4(FLNB):c.199C>T (p.His67Tyr) rs751371914
NM_001457.4(FLNB):c.219_222dup (p.Met75fs)
NM_001457.4(FLNB):c.2251G>C (p.Gly751Arg) rs28937587
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.2772del (p.Thr923_Tyr924insTer)
NM_001457.4(FLNB):c.2996G>A (p.Arg999Gln) rs755928543
NM_001457.4(FLNB):c.3127-354_4223-1836del
NM_001457.4(FLNB):c.3173C>T (p.Pro1058Leu)
NM_001457.4(FLNB):c.3446_3455del (p.Gly1149fs) rs1553701033
NM_001457.4(FLNB):c.3535G>T (p.Glu1179Ter)
NM_001457.4(FLNB):c.4229C>G (p.Pro1410Arg) rs2107204256
NM_001457.4(FLNB):c.4292T>G (p.Leu1431Arg) rs80356511
NM_001457.4(FLNB):c.4391G>C (p.Gly1464Ala) rs886044175
NM_001457.4(FLNB):c.4427A>G (p.Asp1476Gly)
NM_001457.4(FLNB):c.442T>A (p.Trp148Arg) rs80356493
NM_001457.4(FLNB):c.4550C>A (p.Ala1517Asp) rs372940610
NM_001457.4(FLNB):c.4570G>A (p.Gly1524Ser) rs2107220190
NM_001457.4(FLNB):c.4570G>C (p.Gly1524Arg)
NM_001457.4(FLNB):c.4585T>C (p.Ser1529Pro) rs770433500
NM_001457.4(FLNB):c.4589A>G (p.Tyr1530Cys) rs776043627
NM_001457.4(FLNB):c.4604G>A (p.Ser1535Asn)
NM_001457.4(FLNB):c.4625T>C (p.Ile1542Thr) rs1356745912
NM_001457.4(FLNB):c.4713_4715del (p.Asn1571del) rs80356512
NM_001457.4(FLNB):c.4747_4749del (p.Asp1583del) rs80356498
NM_001457.4(FLNB):c.4756G>A (p.Gly1586Arg) rs80356513
NM_001457.4(FLNB):c.4768_4771del (p.Ile1590fs) rs1553703909
NM_001457.4(FLNB):c.4775T>A (p.Val1592Asp) rs80356514
NM_001457.4(FLNB):c.4804T>C (p.Ser1602Pro) rs80356501
NM_001457.4(FLNB):c.4805C>A (p.Ser1602Tyr) rs2107224888
NM_001457.4(FLNB):c.4807C>T (p.Pro1603Ser) rs2107224894
NM_001457.4(FLNB):c.4808C>T (p.Pro1603Leu) rs80356515
NM_001457.4(FLNB):c.482T>G (p.Phe161Cys) rs80356506
NM_001457.4(FLNB):c.4927G>T (p.Ala1643Ser) rs80356502
NM_001457.4(FLNB):c.4928C>T (p.Ala1643Val) rs868820857
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.502G>A (p.Gly168Ser) rs80356504
NM_001457.4(FLNB):c.5071G>A (p.Gly1691Ser) rs80356503
NM_001457.4(FLNB):c.5072G>A (p.Gly1691Asp) rs1553704446
NM_001457.4(FLNB):c.512T>A (p.Leu171Gln) rs80356494
NM_001457.4(FLNB):c.512T>G (p.Leu171Arg) rs80356494
NM_001457.4(FLNB):c.517G>A (p.Ala173Thr) rs587777259
NM_001457.4(FLNB):c.518C>T (p.Ala173Val) rs121908894
NM_001457.4(FLNB):c.542G>T (p.Gly181Val) rs80356495
NM_001457.4(FLNB):c.545T>G (p.Leu182Arg)
NM_001457.4(FLNB):c.5465G>A (p.Gly1822Glu)
NM_001457.4(FLNB):c.549C>G (p.Cys183Trp) rs80356496
NM_001457.4(FLNB):c.5500G>A (p.Gly1834Arg) rs80356516
NM_001457.4(FLNB):c.5524T>C (p.Phe1842Leu) rs1178860596
NM_001457.4(FLNB):c.5548G>T (p.Gly1850Ter) rs121908898
NM_001457.4(FLNB):c.5555-5_5561del rs1575457582
NM_001457.4(FLNB):c.5696T>A (p.Ile1899Asn)
NM_001457.4(FLNB):c.5842C>T (p.Arg1948Ter) rs775301566
NM_001457.4(FLNB):c.591T>A (p.Asn197Lys) rs1274950884
NM_001457.4(FLNB):c.6010C>T (p.Arg2004Ter) rs121908897
NM_001457.4(FLNB):c.602C>T (p.Ala201Val) rs80356499
NM_001457.4(FLNB):c.604A>G (p.Met202Val) rs121908895
NM_001457.4(FLNB):c.608A>C (p.Gln203Pro) rs80356497
NM_001457.4(FLNB):c.629G>T (p.Gly210Val) rs80356500
NM_001457.4(FLNB):c.6408del (p.Ser2137fs) rs80356521
NM_001457.4(FLNB):c.644T>A (p.Ile215Asn) rs2097209399
NM_001457.4(FLNB):c.6643A>G (p.Ser2215Gly) rs2097350829
NM_001457.4(FLNB):c.679G>A (p.Glu227Lys) rs80356508
NM_001457.4(FLNB):c.6866G>A (p.Arg2289His) rs1033252725
NM_001457.4(FLNB):c.698del (p.Tyr233fs)
NM_001457.4(FLNB):c.6994G>A (p.Glu2332Lys)
NM_001457.4(FLNB):c.700C>G (p.Leu234Val) rs80356507
NM_001457.4(FLNB):c.7029T>G (p.Tyr2343Ter) rs80356518
NM_001457.4(FLNB):c.703T>C (p.Ser235Pro) rs121908896
NM_001457.4(FLNB):c.7351C>G (p.Leu2451Val) rs2107340030
NM_001457.4(FLNB):c.7624T>C (p.Ser2542Pro)
NM_001457.4(FLNB):c.7760G>T (p.Trp2587Leu) rs144321868

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