ClinVar Miner

List of variants in gene FLNC reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 127
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.4404T>C (p.Asp1468=) rs2249128 0.99086
NM_001458.5(FLNC):c.5398+16T>C rs13227216 0.32203
NM_001458.5(FLNC):c.3973C>T (p.Leu1325=) rs34373805 0.28610
NM_001458.5(FLNC):c.3297A>G (p.Val1099=) rs3734973 0.28603
NM_001458.5(FLNC):c.5763T>C (p.Thr1921=) rs3816884 0.18399
NM_001458.5(FLNC):c.2265+12C>G rs2291566 0.17192
NM_001458.5(FLNC):c.1814-28T>C rs2291565 0.16389
NM_001458.5(FLNC):c.7221C>T (p.Asp2407=) rs3816885 0.15729
NM_001458.5(FLNC):c.4431G>A (p.Leu1477=) rs2291568 0.15512
NM_001458.5(FLNC):c.1032C>T (p.Val344=) rs2291562 0.12206
NM_001458.5(FLNC):c.1458C>A (p.Pro486=) rs2291563 0.11830
NM_001458.5(FLNC):c.720T>C (p.Ile240=) rs2291560 0.11080
NM_001458.5(FLNC):c.795T>C (p.Gly265=) rs2291561 0.10971
NM_001458.5(FLNC):c.147C>T (p.His49=) rs3734972 0.09267
NM_001458.5(FLNC):c.4056C>T (p.Arg1352=) rs75770585 0.08775
NM_001458.5(FLNC):c.850+18G>A rs55907818 0.08058
NM_001458.5(FLNC):c.3624G>A (p.Ala1208=) rs35281128 0.06868
NM_001458.5(FLNC):c.4700G>A (p.Arg1567Gln) rs2291569 0.06258
NM_001458.5(FLNC):c.*1A>G rs114713626 0.05145
NM_001458.5(FLNC):c.3838C>T (p.Leu1280=) rs34180031 0.03419
NM_001458.5(FLNC):c.1614C>T (p.Tyr538=) rs76046880 0.02993
NM_001458.5(FLNC):c.2390-13C>T rs78086167 0.02800
NM_001458.5(FLNC):c.5669-12C>T rs79790270 0.02786
NM_001458.5(FLNC):c.8121T>C (p.Ile2707=) rs28437296 0.01520
NM_001458.5(FLNC):c.1374C>T (p.Pro458=) rs115140972 0.01514
NM_001458.5(FLNC):c.8118C>T (p.Leu2706=) rs28379666 0.01465
NM_001458.5(FLNC):c.6004+19G>A rs12530507 0.01231
NM_001458.5(FLNC):c.2266-14G>C rs75612085 0.01030
NM_001458.5(FLNC):c.4302C>T (p.Arg1434=) rs114697352 0.00988
NM_001458.5(FLNC):c.2390-14C>T rs71581921 0.00843
NM_001458.5(FLNC):c.6771A>G (p.Pro2257=) rs34422412 0.00842
NM_001458.5(FLNC):c.3852C>T (p.Gly1284=) rs111337293 0.00743
NM_001458.5(FLNC):c.4289-4A>C rs140031589 0.00743
NM_001458.5(FLNC):c.3721C>T (p.Arg1241Cys) rs146953558 0.00728
NM_001458.5(FLNC):c.6004+11G>A rs117653869 0.00719
NM_001458.5(FLNC):c.352+10G>A rs79489893 0.00639
NM_001458.5(FLNC):c.-12G>T rs199842696 0.00599
NM_001458.5(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717 0.00536
NM_001458.5(FLNC):c.1902G>A (p.Glu634=) rs12536635 0.00414
NM_001458.5(FLNC):c.1549+15C>A rs181134489 0.00403
NM_001458.5(FLNC):c.1425C>T (p.Asn475=) rs143610360 0.00297
NM_001458.5(FLNC):c.2078A>C (p.Asp693Ala) rs34972246 0.00297
NM_001458.5(FLNC):c.8003T>C (p.Met2668Thr) rs200502811 0.00291
NM_001458.5(FLNC):c.4928-7T>C rs201957008 0.00286
NM_001458.5(FLNC):c.3006G>A (p.Arg1002=) rs61737781 0.00283
NM_001458.5(FLNC):c.7780+10A>G rs201149834 0.00281
NM_001458.5(FLNC):c.4737+15A>G rs182734223 0.00252
NM_001458.5(FLNC):c.2889G>A (p.Pro963=) rs191892345 0.00212
NM_001458.5(FLNC):c.2507C>A (p.Pro836Gln) rs199652368 0.00207
NM_001458.5(FLNC):c.561C>T (p.Asp187=) rs149474376 0.00178
NM_001458.5(FLNC):c.7091G>A (p.Arg2364His) rs201672146 0.00173
NM_001458.5(FLNC):c.2390-9T>C rs368068407 0.00168
NM_001458.5(FLNC):c.8049C>T (p.Tyr2683=) rs183104951 0.00165
NM_001458.5(FLNC):c.5644A>G (p.Ile1882Val) rs184018403 0.00160
NM_001458.5(FLNC):c.2389+12C>T rs370526829 0.00151
NM_001458.5(FLNC):c.4456+14G>A rs375227447 0.00144
NM_001458.5(FLNC):c.6714C>T (p.Thr2238=) rs10268251 0.00143
NM_001458.5(FLNC):c.3861C>T (p.His1287=) rs375986462 0.00142
NM_001458.5(FLNC):c.5262C>T (p.Tyr1754=) rs369165766 0.00139
NM_001458.5(FLNC):c.1577G>A (p.Arg526Gln) rs34932223 0.00138
NM_001458.5(FLNC):c.2501C>T (p.Thr834Met) rs75133741 0.00136
NM_001458.5(FLNC):c.6459C>T (p.Thr2153=) rs113618587 0.00135
NM_001458.5(FLNC):c.6005-9T>C rs118124743 0.00133
NM_001458.5(FLNC):c.1813+11G>T rs138716837 0.00126
NM_001458.5(FLNC):c.597C>T (p.Ala199=) rs143942649 0.00124
NM_001458.5(FLNC):c.2180G>A (p.Arg727His) rs200618242 0.00120
NM_001458.5(FLNC):c.4947C>T (p.Gly1649=) rs201069454 0.00119
NM_001458.5(FLNC):c.6309C>T (p.Thr2103=) rs376992044 0.00116
NM_001458.5(FLNC):c.3000T>C (p.Asp1000=) rs184454068 0.00110
NM_001458.5(FLNC):c.5766G>A (p.Ala1922=) rs58914363 0.00108
NM_001458.5(FLNC):c.6998-5C>T rs139030003 0.00106
NM_001458.5(FLNC):c.6362-17C>G rs368901431 0.00094
NM_001458.5(FLNC):c.5418G>A (p.Ser1806=) rs376078394 0.00090
NM_001458.5(FLNC):c.7947C>T (p.Phe2649=) rs368849358 0.00083
NM_001458.5(FLNC):c.7990+9C>T rs566679569 0.00077
NM_001458.5(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783 0.00068
NM_001458.5(FLNC):c.4456+13C>T rs200456962 0.00065
NM_001458.5(FLNC):c.3621C>T (p.Asn1207=) rs117864464 0.00063
NM_001458.5(FLNC):c.3757G>A (p.Val1253Ile) rs117366477 0.00051
NM_001458.5(FLNC):c.5592C>T (p.Ala1864=) rs117517372 0.00048
NM_001458.5(FLNC):c.3966C>T (p.Gly1322=) rs200237564 0.00045
NM_001458.5(FLNC):c.5764G>A (p.Ala1922Thr) rs202128602 0.00040
NM_001458.5(FLNC):c.6120C>T (p.Asp2040=) rs116974302 0.00039
NM_001458.5(FLNC):c.7991-19C>T rs537052947 0.00034
NM_001458.5(FLNC):c.2568C>T (p.Pro856=) rs201611050 0.00032
NM_001458.5(FLNC):c.294G>A (p.Glu98=) rs201839252 0.00029
NM_001458.5(FLNC):c.5367C>T (p.Ile1789=) rs377214486 0.00026
NM_001458.5(FLNC):c.2733G>A (p.Lys911=) rs374135903 0.00024
NM_001458.5(FLNC):c.1434C>T (p.Arg478=) rs201810745 0.00023
NM_001458.5(FLNC):c.6888C>T (p.His2296=) rs375259002 0.00017
NM_001458.5(FLNC):c.1923C>T (p.His641=) rs375361259 0.00016
NM_001458.5(FLNC):c.4153C>T (p.Leu1385=) rs202125701 0.00016
NM_001458.5(FLNC):c.96G>A (p.Ala32=) rs368239688 0.00016
NM_001458.5(FLNC):c.3090C>T (p.Pro1030=) rs760926290 0.00013
NM_001458.5(FLNC):c.600C>T (p.Pro200=) rs202105410 0.00013
NM_001458.5(FLNC):c.1813+12G>A rs750404224 0.00010
NM_001458.5(FLNC):c.2841C>T (p.Gly947=) rs547060988 0.00010
NM_001458.5(FLNC):c.4952-9G>T rs747821376 0.00010
NM_001458.5(FLNC):c.5445C>T (p.Thr1815=) rs758995789 0.00010
NM_001458.5(FLNC):c.602-11C>T rs371111092 0.00010
NM_001458.5(FLNC):c.2292C>T (p.Pro764=) rs369916201 0.00009
NM_001458.5(FLNC):c.4161C>T (p.Ile1387=) rs200288149 0.00009
NM_001458.5(FLNC):c.4914G>A (p.Lys1638=) rs371385321 0.00009
NM_001458.5(FLNC):c.4488T>C (p.Asn1496=) rs377258966 0.00008
NM_001458.5(FLNC):c.6988G>A (p.Gly2330Ser) rs527248119 0.00008
NM_001458.5(FLNC):c.6114C>T (p.Ile2038=) rs559639511 0.00006
NM_001458.5(FLNC):c.2490C>T (p.Thr830=) rs777580254 0.00005
NM_001458.5(FLNC):c.6864C>T (p.Val2288=) rs761269440 0.00004
NM_001458.5(FLNC):c.602-16T>A rs1236096502 0.00003
NM_001458.5(FLNC):c.7545C>T (p.Leu2515=) rs369791058 0.00003
NM_001458.5(FLNC):c.1209G>A (p.Ala403=) rs746938160 0.00002
NM_001458.5(FLNC):c.558G>A (p.Gln186=) rs532206394 0.00002
NM_001458.5(FLNC):c.2982C>T (p.Gly994=) rs947174901 0.00001
NM_001458.5(FLNC):c.3506A>G (p.Lys1169Arg) rs530742766 0.00001
NM_001458.5(FLNC):c.7385-5C>T rs367793265 0.00001
NM_001458.5(FLNC):c.8136C>T (p.Asp2712=) rs748104907 0.00001
NM_001458.5(FLNC):c.-26_-9dup rs749265933
NM_001458.5(FLNC):c.3765C>A (p.Val1255=) rs556428588
NM_001458.5(FLNC):c.4456+16G>A rs543476754
NM_001458.5(FLNC):c.4737+9_4737+10del rs794727437
NM_001458.5(FLNC):c.4812G>A (p.Pro1604=) rs553400393
NM_001458.5(FLNC):c.5042C>G (p.Thr1681Arg) rs193159707
NM_001458.5(FLNC):c.5399-17C>T rs930809365
NM_001458.5(FLNC):c.7609G>A (p.Ala2537Thr) rs201486752
NM_001458.5(FLNC):c.7990+19G>T rs534098005
NM_001458.5(FLNC):c.8118_8121delinsTATC (p.Leu2706_Ile2707=) rs2128940705
NM_001458.5(FLNC):c.969+14G>T rs765545958

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.