ClinVar Miner

List of variants in gene FLNB reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 125
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.4173A>G (p.Ala1391=) rs2362903 0.72429
NM_001457.4(FLNB):c.6889-18G>A rs12634123 0.62957
NM_001457.4(FLNB):c.927T>C (p.Ser309=) rs1522384 0.42973
NM_001457.4(FLNB):c.4221C>T (p.Pro1407=) rs2362904 0.42377
NM_001457.4(FLNB):c.4411G>A (p.Val1471Met) rs12632456 0.38984
NM_001457.4(FLNB):c.7359C>T (p.Ser2453=) rs8640 0.36629
NM_001457.4(FLNB):c.3469G>A (p.Asp1157Asn) rs1131356 0.33365
NM_001457.4(FLNB):c.7209G>A (p.Ser2403=) rs13079906 0.09018
NM_001457.4(FLNB):c.1869C>T (p.Asp623=) rs2140104 0.04479
NM_001457.4(FLNB):c.1611-4G>A rs73074072 0.04164
NM_001457.4(FLNB):c.6438G>A (p.Val2146=) rs60599272 0.03073
NM_001457.4(FLNB):c.3857C>T (p.Ala1286Val) rs62621997 0.02930
NM_001457.4(FLNB):c.792C>T (p.Ile264=) rs7623314 0.02745
NM_001457.4(FLNB):c.3535G>A (p.Glu1179Lys) rs17058845 0.02351
NM_001457.4(FLNB):c.292+8C>A rs9831243 0.01775
NM_001457.4(FLNB):c.4062-5T>G rs3732632 0.01225
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.3771G>A (p.Pro1257=) rs146851485 0.00794
NM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr) rs116826041 0.00739
NM_001457.4(FLNB):c.2907G>A (p.Arg969=) rs138449267 0.00724
NM_001457.4(FLNB):c.249G>A (p.Ala83=) rs112750785 0.00622
NM_001457.4(FLNB):c.720C>T (p.Ala240=) rs111433950 0.00554
NM_001457.4(FLNB):c.669G>A (p.Pro223=) rs140815373 0.00527
NM_001457.4(FLNB):c.5646G>A (p.Pro1882=) rs114882667 0.00522
NM_001457.4(FLNB):c.3785G>C (p.Gly1262Ala) rs111330368 0.00503
NM_001457.4(FLNB):c.7099G>A (p.Val2367Ile) rs115747856 0.00488
NM_001457.4(FLNB):c.3078C>T (p.Pro1026=) rs147267045 0.00465
NM_001457.4(FLNB):c.4671+11G>A rs115346578 0.00454
NM_001457.4(FLNB):c.4872C>T (p.Ile1624=) rs147426569 0.00436
NM_001457.4(FLNB):c.3090C>T (p.Tyr1030=) rs112968165 0.00406
NM_001457.4(FLNB):c.2382C>T (p.Asp794=) rs146159035 0.00360
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=) rs77989135 0.00333
NM_001457.4(FLNB):c.3264C>T (p.Ser1088=) rs112864468 0.00322
NM_001457.4(FLNB):c.4222+19A>C rs146229370 0.00319
NM_001457.4(FLNB):c.362A>T (p.Tyr121Phe) rs147846832 0.00269
NM_001457.4(FLNB):c.5426-10G>A rs183917041 0.00264
NM_001457.4(FLNB):c.292+14C>G rs200721532 0.00260
NM_001457.4(FLNB):c.1044C>T (p.Asp348=) rs111996979 0.00252
NM_001457.4(FLNB):c.4222+8A>G rs190025781 0.00248
NM_001457.4(FLNB):c.4377T>C (p.Val1459=) rs149921907 0.00232
NM_001457.4(FLNB):c.4362G>A (p.Pro1454=) rs150844992 0.00217
NM_001457.4(FLNB):c.5091C>T (p.Asn1697=) rs141357606 0.00199
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=) rs145280904 0.00184
NM_001457.4(FLNB):c.6147G>A (p.Thr2049=) rs146271686 0.00155
NM_001457.4(FLNB):c.6773-13C>A rs200653965 0.00149
NM_001457.4(FLNB):c.6741G>A (p.Ser2247=) rs143400214 0.00142
NM_001457.4(FLNB):c.420G>A (p.Thr140=) rs192491895 0.00134
NM_001457.4(FLNB):c.6000T>C (p.Gly2000=) rs140926445 0.00127
NM_001457.4(FLNB):c.7668C>T (p.Cys2556=) rs144621434 0.00125
NM_001457.4(FLNB):c.293-17T>G rs199821588 0.00078
NM_001457.4(FLNB):c.292+12G>C rs201148582 0.00066
NM_001457.4(FLNB):c.4672-11A>G rs72884428 0.00064
NM_001457.4(FLNB):c.6843C>T (p.Ile2281=) rs140332932 0.00062
NM_001457.4(FLNB):c.6680C>G (p.Ser2227Cys) rs138327769 0.00050
NM_001457.4(FLNB):c.1704G>A (p.Ala568=) rs139001948 0.00043
NM_001457.4(FLNB):c.4730C>T (p.Ala1577Val) rs148101195 0.00043
NM_001457.4(FLNB):c.3873G>C (p.Gln1291His) rs574189101 0.00033
NM_001457.4(FLNB):c.7254C>T (p.Ser2418=) rs563382903 0.00031
NM_001457.4(FLNB):c.7255G>A (p.Val2419Ile) rs202143851 0.00024
NM_001457.4(FLNB):c.5887+8A>G rs143066905 0.00023
NM_001457.4(FLNB):c.1534G>A (p.Ala512Thr) rs201544295 0.00022
NM_001457.4(FLNB):c.3898+19G>A rs780062399 0.00021
NM_001457.4(FLNB):c.1930A>G (p.Asn644Asp) rs146859540 0.00019
NM_001457.4(FLNB):c.5445C>T (p.Tyr1815=) rs755702006 0.00019
NM_001457.4(FLNB):c.5769C>T (p.Ala1923=) rs201723447 0.00019
NM_001457.4(FLNB):c.7198+20C>G rs201580886 0.00019
NM_001457.4(FLNB):c.4390+8T>A rs377095569 0.00018
NM_001457.4(FLNB):c.5785G>A (p.Asp1929Asn) rs146685642 0.00017
NM_001457.4(FLNB):c.1868A>T (p.Asp623Val) rs145314043 0.00016
NM_001457.4(FLNB):c.5506G>A (p.Ala1836Thr) rs199964133 0.00015
NM_001457.4(FLNB):c.1290C>G (p.Ile430Met) rs147854989 0.00014
NM_001457.4(FLNB):c.2931G>A (p.Leu977=) rs574484752 0.00012
NM_001457.4(FLNB):c.3476C>T (p.Ser1159Leu) rs201254275 0.00011
NM_001457.4(FLNB):c.2035C>T (p.Pro679Ser) rs144158201 0.00010
NM_001457.4(FLNB):c.7003G>A (p.Val2335Met) rs147537617 0.00009
NM_001457.4(FLNB):c.5220C>T (p.Asn1740=) rs531970315 0.00008
NM_001457.4(FLNB):c.5532C>T (p.Ile1844=) rs202240037 0.00008
NM_001457.4(FLNB):c.1873G>A (p.Glu625Lys) rs372998485 0.00007
NM_001457.4(FLNB):c.6221A>G (p.Lys2074Arg) rs148043654 0.00007
NM_001457.4(FLNB):c.6634+8T>C rs200284480 0.00007
NM_001457.4(FLNB):c.6728A>G (p.His2243Arg) rs184329174 0.00007
NM_001457.4(FLNB):c.7424G>A (p.Arg2475His) rs568474038 0.00007
NM_001457.4(FLNB):c.1946G>A (p.Arg649Gln) rs145910735 0.00006
NM_001457.4(FLNB):c.6463G>A (p.Val2155Ile) rs371871707 0.00006
NM_001457.4(FLNB):c.3930C>T (p.Asp1310=) rs150901141 0.00004
NM_001457.4(FLNB):c.5740C>T (p.Arg1914Trp) rs769582613 0.00004
NM_001457.4(FLNB):c.1278C>T (p.His426=) rs572259451 0.00003
NM_001457.4(FLNB):c.3265G>A (p.Asp1089Asn) rs369045614 0.00003
NM_001457.4(FLNB):c.1107C>T (p.Asn369=) rs538953239 0.00002
NM_001457.4(FLNB):c.3787G>A (p.Gly1263Ser) rs769722241 0.00002
NM_001457.4(FLNB):c.6829C>T (p.Leu2277=) rs150602768 0.00002
NM_001457.4(FLNB):c.7749G>A (p.Leu2583=) rs535252967 0.00002
NM_001457.4(FLNB):c.6755A>T (p.Tyr2252Phe) rs200567066 0.00001
NM_001457.4(FLNB):c.107G>A (p.Arg36His) rs142568031
NM_001457.4(FLNB):c.1327G>C (p.Val443Leu) rs200902568
NM_001457.4(FLNB):c.1710C>T (p.Phe570=)
NM_001457.4(FLNB):c.2162T>C (p.Val721Ala)
NM_001457.4(FLNB):c.2622G>T (p.Gly874=)
NM_001457.4(FLNB):c.2644G>T (p.Val882Leu)
NM_001457.4(FLNB):c.2745+17C>G rs377054671
NM_001457.4(FLNB):c.3163G>T (p.Val1055Leu) rs9813235
NM_001457.4(FLNB):c.3466G>A (p.Val1156Ile)
NM_001457.4(FLNB):c.3477G>A (p.Ser1159=)
NM_001457.4(FLNB):c.3479A>T (p.Glu1160Val)
NM_001457.4(FLNB):c.3631G>A (p.Glu1211Lys)
NM_001457.4(FLNB):c.3724+35_3724+36del rs56147140
NM_001457.4(FLNB):c.3724+36dup
NM_001457.4(FLNB):c.3779A>C (p.Gln1260Pro)
NM_001457.4(FLNB):c.4050C>A (p.Thr1350=)
NM_001457.4(FLNB):c.4515-24GT[4] rs151085835
NM_001457.4(FLNB):c.4813C>T (p.Arg1605Cys)
NM_001457.4(FLNB):c.5042C>G (p.Pro1681Arg) rs780823510
NM_001457.4(FLNB):c.5134G>T (p.Val1712Leu) rs138141099
NM_001457.4(FLNB):c.5233A>C (p.Lys1745Gln)
NM_001457.4(FLNB):c.5343C>T (p.Asp1781=)
NM_001457.4(FLNB):c.5526C>T (p.Phe1842=)
NM_001457.4(FLNB):c.6576C>T (p.Gly2192=)
NM_001457.4(FLNB):c.6634+11C>T rs374708033
NM_001457.4(FLNB):c.6745G>A (p.Gly2249Ser)
NM_001457.4(FLNB):c.7021+24dup
NM_001457.4(FLNB):c.7369G>A (p.Gly2457Ser)
NM_001457.4(FLNB):c.7387G>T (p.Val2463Leu)
NM_001457.4(FLNB):c.7488G>A (p.Ser2496=)
NM_001457.4(FLNB):c.984+15C>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.