ClinVar Miner

List of variants in gene FLNB reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.906+267T>G rs77546328 0.03237
NM_001457.4(FLNB):c.3725-208C>T rs75371794 0.03232
NM_001457.4(FLNB):c.2745+203T>C rs74562361 0.02235
NM_001457.4(FLNB):c.984+194C>G rs17058819 0.02234
NM_001457.4(FLNB):c.6091+246C>T rs77235099 0.02160
NM_001457.4(FLNB):c.4514+204C>G rs144894047 0.02043
NM_001457.4(FLNB):c.3127-277G>T rs35327008 0.01907
NM_001457.4(FLNB):c.4062-300C>T rs116496081 0.01455
NM_001457.4(FLNB):c.4861+142G>A rs75228448 0.01425
NM_001457.4(FLNB):c.4671+154G>T rs9848629 0.01344
NM_001457.4(FLNB):c.5426-236C>T rs79747308 0.01263
NM_001457.4(FLNB):c.1748-210G>T rs146387779 0.01240
NM_001457.4(FLNB):c.6773-244G>C rs116115589 0.01239
NM_001457.4(FLNB):c.7418-176T>C rs138736092 0.01231
NM_001457.4(FLNB):c.1484-195A>C rs74712521 0.01212
NM_001457.4(FLNB):c.6092-239C>T rs115342997 0.01204
NM_001457.4(FLNB):c.3724+116C>T rs17058846 0.01130
NM_001457.4(FLNB):c.3898+171G>T rs116610948 0.01127
NM_001457.4(FLNB):c.3898+172C>T rs76360456 0.01126
NM_001457.4(FLNB):c.4391-604C>T rs17058879 0.01111
NM_001457.4(FLNB):c.1747+184G>C rs75277188 0.01097
NM_001457.4(FLNB):c.1611-171A>G rs3817448 0.01090
NM_001457.4(FLNB):c.2323+73T>C rs548730080 0.01067
NM_001457.4(FLNB):c.5555-279G>A rs140925269 0.01063
NM_001457.4(FLNB):c.1483+131C>G rs76971603 0.01059
NM_001457.4(FLNB):c.7621+264G>A rs78103805 0.01032
NM_001457.4(FLNB):c.906+106A>G rs114460813 0.01022
NM_001457.4(FLNB):c.2055+262G>A rs116668062 0.01012
NM_001457.4(FLNB):c.1483+35G>A rs74824935 0.00986
NM_001457.4(FLNB):c.2864-309dup rs202093084 0.00978
NM_001457.4(FLNB):c.5426-272_5426-271insAT rs10663545 0.00858
NM_001457.4(FLNB):c.5426-50G>A rs143795134 0.00811
NM_001457.4(FLNB):c.3724+13_3724+15del rs773897420 0.00809
NM_001457.4(FLNB):c.5728+95G>A rs75827811 0.00756
NM_001457.4(FLNB):c.3898+116G>A rs17058848 0.00743
NM_001457.4(FLNB):c.6092-324C>T rs113246208 0.00735
NM_001457.4(FLNB):c.4222+165del rs367954179 0.00721
NM_001457.4(FLNB):c.3899-24G>A rs114259778 0.00712
NM_001457.4(FLNB):c.4391-711C>T rs17058877 0.00706
NM_001457.4(FLNB):c.4391-645C>T rs79380986 0.00704
NM_001457.4(FLNB):c.7418-107C>T rs111281532 0.00701
NC_000003.12:g.58008096T>C rs115081474 0.00691
NM_001457.4(FLNB):c.6635-97A>G rs9856520 0.00666
NM_001457.4(FLNB):c.292+283G>A rs114032500 0.00648
NM_001457.4(FLNB):c.541+102G>A rs115199080 0.00645
NM_001457.4(FLNB):c.5109+154A>G rs9827587 0.00601
NM_001457.4(FLNB):c.1148-188G>A rs7640352 0.00595
NM_001457.4(FLNB):c.4390+113A>T rs181343883 0.00551
NM_001457.4(FLNB):c.7417+170G>A rs28595232 0.00540
NM_001457.4(FLNB):c.7418-272G>C rs142738612 0.00529
NM_001457.4(FLNB):c.4390+861T>G rs78445950 0.00493
NM_001457.4(FLNB):c.4391-596G>A rs144200627 0.00471
NM_001457.4(FLNB):c.5181+161G>A rs11130614 0.00466
NM_001457.4(FLNB):c.5181+292G>A rs186505894 0.00420
NM_001457.4(FLNB):c.3127-230G>A rs78943929 0.00407
NM_001457.4(FLNB):c.2055+252G>A rs116135152 0.00394
NM_001457.4(FLNB):c.6888+34G>A rs115601424 0.00389
NM_001457.4(FLNB):c.5110-183_5110-182del rs568656017 0.00387
NM_001457.4(FLNB):c.2864-72C>T rs60215678 0.00343
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=) rs77989135 0.00333
NM_001457.4(FLNB):c.787+26A>G rs199540800 0.00332
NM_001457.4(FLNB):c.4222+19A>C rs146229370 0.00319
NM_001457.4(FLNB):c.292+14C>G rs200721532 0.00260
NM_001457.4(FLNB):c.4222+8A>G rs190025781 0.00248
NM_001457.4(FLNB):c.1559C>T (p.Pro520Leu) rs138220431 0.00247
NM_001457.4(FLNB):c.4377T>C (p.Val1459=) rs149921907 0.00232
NM_001457.4(FLNB):c.274A>G (p.Ile92Val) rs62622011 0.00229
NM_001457.4(FLNB):c.1345+267C>T rs189510734 0.00227
NM_001457.4(FLNB):c.4362G>A (p.Pro1454=) rs150844992 0.00217
NM_001457.4(FLNB):c.1472T>C (p.Met491Thr) rs147575358 0.00203
NM_001457.4(FLNB):c.6244+4T>G rs185737810 0.00178
NM_001457.4(FLNB):c.6888+44A>G rs192272412 0.00178
NM_001457.4(FLNB):c.6773-13C>A rs200653965 0.00149
NM_001457.4(FLNB):c.4929C>T (p.Ala1643=) rs149070858 0.00140
NM_001457.4(FLNB):c.3169A>C (p.Lys1057Gln) rs13321615 0.00133
NM_001457.4(FLNB):c.6000T>C (p.Gly2000=) rs140926445 0.00127
NM_001457.4(FLNB):c.6047G>A (p.Arg2016Gln) rs137885421 0.00117
NM_001457.4(FLNB):c.1697G>A (p.Arg566Gln) rs150747960 0.00098
NM_001457.4(FLNB):c.808A>G (p.Met270Val) rs145036794 0.00096
NM_001457.4(FLNB):c.1998C>T (p.Ala666=) rs143161769 0.00088
NM_001457.4(FLNB):c.6315C>T (p.Ala2105=) rs147648427 0.00079
NM_001457.4(FLNB):c.3288C>T (p.Ser1096=) rs77934864 0.00071
NM_001457.4(FLNB):c.4022C>G (p.Ala1341Gly) rs139269734 0.00068
NM_001457.4(FLNB):c.292+12G>C rs201148582 0.00066
NM_001457.4(FLNB):c.4233C>G (p.Phe1411Leu) rs143831841 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.7530G>A (p.Ser2510=) rs141700862 0.00056
NM_001457.4(FLNB):c.4495G>A (p.Asp1499Asn) rs150445941 0.00046
NM_001457.4(FLNB):c.1196A>G (p.Lys399Arg) rs145673747 0.00043
NM_001457.4(FLNB):c.1704G>A (p.Ala568=) rs139001948 0.00043
NM_001457.4(FLNB):c.6072C>T (p.Ile2024=) rs144036986 0.00036
NM_001457.4(FLNB):c.3981G>A (p.Gln1327=) rs201441533 0.00033
NM_001457.4(FLNB):c.4061+4G>A rs370061963 0.00032
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.3583G>A (p.Val1195Met) rs200993986 0.00021
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.3753T>C (p.Phe1251=) rs751650356 0.00011
NM_001457.4(FLNB):c.762G>A (p.Pro254=) rs371715057 0.00011
NM_001457.4(FLNB):c.4281C>T (p.Ala1427=) rs188516921 0.00009
NM_001457.4(FLNB):c.6666C>T (p.Gly2222=) rs144628013 0.00008
NM_001457.4(FLNB):c.7164C>T (p.Ser2388=) rs757418085 0.00006
NM_001457.4(FLNB):c.4287C>T (p.Pro1429=) rs376873981 0.00005
NM_001457.4(FLNB):c.2935G>A (p.Val979Met) rs376511120 0.00004
NM_001457.4(FLNB):c.4671+5C>G rs776434196 0.00004
NM_001457.4(FLNB):c.541+15C>T rs770019318 0.00004
NM_001457.4(FLNB):c.6003C>T (p.Asp2001=) rs184065600 0.00004
NM_001457.4(FLNB):c.1101A>G (p.Val367=) rs199596463 0.00001
NM_001457.4(FLNB):c.282C>T (p.Leu94=) rs745493076 0.00001
NM_001457.4(FLNB):c.5181+17T>C rs367874839 0.00001
NM_001457.4(FLNB):c.787+14C>T rs1421148550 0.00001
NM_001457.4(FLNB):c.9A>G (p.Val3=) rs199846967 0.00001
NC_000003.12:g.58008288G>A rs541297257
NM_001457.4(FLNB):c.107G>A (p.Arg36His) rs142568031
NM_001457.4(FLNB):c.1483+148G>C rs75243235
NM_001457.4(FLNB):c.1941+139TTTG[7] rs543270582
NM_001457.4(FLNB):c.1942-243C>T rs114667821
NM_001457.4(FLNB):c.1942-323dup rs199822091
NM_001457.4(FLNB):c.2637G>C (p.Pro879=) rs149334776
NM_001457.4(FLNB):c.3163G>A (p.Val1055Met) rs9813235
NM_001457.4(FLNB):c.4390+199C>A rs61680876
NM_001457.4(FLNB):c.4515-24GT[4] rs151085835
NM_001457.4(FLNB):c.5037C>T (p.Ala1679=) rs770779551
NM_001457.4(FLNB):c.5109+326_5109+327del rs10575648
NM_001457.4(FLNB):c.5425+76G>A rs143171743
NM_001457.4(FLNB):c.639+154A>T rs116551325
NM_001457.4(FLNB):c.6635-247C>A rs1224692120
NM_001457.4(FLNB):c.787+236del rs547963189
NM_001457.4(FLNB):c.787+242_787+247del rs556543095
NM_001457.4(FLNB):c.906+276TATT[10] rs1553694995
NM_001457.4(FLNB):c.906+278_906+279insGTATTTATTTATTTAT rs140031981

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.