ClinVar Miner

List of variants in gene FLNC reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NC_000007.14:g.128856236_128856237del
NM_001458.4(FLNC):c.*1A>G rs114713626
NM_001458.4(FLNC):c.-210G>A
NM_001458.4(FLNC):c.-230C>A
NM_001458.4(FLNC):c.-316C>T
NM_001458.4(FLNC):c.1032C>T (p.Val344=) rs2291562
NM_001458.4(FLNC):c.1374C>T (p.Pro458=) rs115140972
NM_001458.4(FLNC):c.1412-159G>A
NM_001458.4(FLNC):c.1412-95C>G
NM_001458.4(FLNC):c.1425C>T (p.Asn475=) rs143610360
NM_001458.4(FLNC):c.1458C>A (p.Pro486=) rs2291563
NM_001458.4(FLNC):c.147C>T (p.His49=) rs3734972
NM_001458.4(FLNC):c.1549+15C>A rs181134489
NM_001458.4(FLNC):c.1577G>A (p.Arg526Gln) rs34932223
NM_001458.4(FLNC):c.1614C>T (p.Tyr538=) rs76046880
NM_001458.4(FLNC):c.1902G>A (p.Glu634=) rs12536635
NM_001458.4(FLNC):c.2078A>C (p.Asp693Ala) rs34972246
NM_001458.4(FLNC):c.2121+181C>T
NM_001458.4(FLNC):c.2121+236A>T
NM_001458.4(FLNC):c.2121+294G>A
NM_001458.4(FLNC):c.2122-17T>C rs144828462
NM_001458.4(FLNC):c.2265+12C>G rs2291566
NM_001458.4(FLNC):c.2390-13C>T rs78086167
NM_001458.4(FLNC):c.2390-14C>T rs71581921
NM_001458.4(FLNC):c.2501C>T (p.Thr834Met) rs75133741
NM_001458.4(FLNC):c.2551-113G>A
NM_001458.4(FLNC):c.3297A>G (p.Val1099=) rs3734973
NM_001458.4(FLNC):c.3506A>G (p.Lys1169Arg) rs530742766
NM_001458.4(FLNC):c.3624G>A (p.Ala1208=) rs35281128
NM_001458.4(FLNC):c.3721C>T (p.Arg1241Cys) rs146953558
NM_001458.4(FLNC):c.3791-194T>G
NM_001458.4(FLNC):c.3838C>T (p.Leu1280=) rs34180031
NM_001458.4(FLNC):c.3852C>T (p.Gly1284=) rs111337293
NM_001458.4(FLNC):c.3973C>T (p.Leu1325=) rs34373805
NM_001458.4(FLNC):c.4056C>T (p.Arg1352=) rs75770585
NM_001458.4(FLNC):c.4161C>T (p.Ile1387=) rs200288149
NM_001458.4(FLNC):c.4288+304T>C
NM_001458.4(FLNC):c.4289-178T>A
NM_001458.4(FLNC):c.4289-4A>C rs140031589
NM_001458.4(FLNC):c.4302C>T (p.Arg1434=) rs114697352
NM_001458.4(FLNC):c.4431G>A (p.Leu1477=) rs2291568
NM_001458.4(FLNC):c.4581-224C>A
NM_001458.4(FLNC):c.4700G>A (p.Arg1567Gln) rs2291569
NM_001458.4(FLNC):c.4928-7T>C rs201957008
NM_001458.4(FLNC):c.5398+16T>C rs13227216
NM_001458.4(FLNC):c.5399-91G>A
NM_001458.4(FLNC):c.5540-120T>C
NM_001458.4(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717
NM_001458.4(FLNC):c.5592C>T (p.Ala1864=) rs117517372
NM_001458.4(FLNC):c.5644A>G (p.Ile1882Val) rs184018403
NM_001458.4(FLNC):c.5669-12C>T rs79790270
NM_001458.4(FLNC):c.5763T>C (p.Thr1921=) rs3816884
NM_001458.4(FLNC):c.5764G>A (p.Ala1922Thr) rs202128602
NM_001458.4(FLNC):c.5842+260G>C
NM_001458.4(FLNC):c.5843-248C>T
NM_001458.4(FLNC):c.5843-87G>A
NM_001458.4(FLNC):c.5843-88G>C
NM_001458.4(FLNC):c.5889G>A (p.Thr1963=) rs374743518
NM_001458.4(FLNC):c.6004+11G>A rs117653869
NM_001458.4(FLNC):c.6004+19G>A rs12530507
NM_001458.4(FLNC):c.6005-9T>C rs118124743
NM_001458.4(FLNC):c.601+203A>G
NM_001458.4(FLNC):c.602-11C>T rs371111092
NM_001458.4(FLNC):c.6120C>T (p.Asp2040=) rs116974302
NM_001458.4(FLNC):c.6208+84C>T
NM_001458.4(FLNC):c.6459C>T (p.Thr2153=) rs113618587
NM_001458.4(FLNC):c.6771A>G (p.Pro2257=) rs34422412
NM_001458.4(FLNC):c.7091G>A (p.Arg2364His) rs201672146
NM_001458.4(FLNC):c.720T>C (p.Ile240=) rs2291560
NM_001458.4(FLNC):c.7221C>T (p.Asp2407=) rs3816885
NM_001458.4(FLNC):c.7251+194G>T
NM_001458.4(FLNC):c.7385-5C>T rs367793265
NM_001458.4(FLNC):c.7545C>T (p.Leu2515=) rs369791058
NM_001458.4(FLNC):c.7781-290G>A
NM_001458.4(FLNC):c.795T>C (p.Gly265=) rs2291561
NM_001458.4(FLNC):c.8049C>T (p.Tyr2683=) rs183104951
NM_001458.4(FLNC):c.8118C>T (p.Leu2706=) rs28379666
NM_001458.4(FLNC):c.8121T>C (p.Ile2707=) rs28437296
NM_001458.4(FLNC):c.850+18G>A rs55907818
NM_001458.4(FLNC):c.969+56G>A
NM_001458.4:c.1814-28T>C

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