ClinVar Miner

List of variants in gene FLNC reported as benign by PreventionGenetics,PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NM_001458.4(FLNC):c.*1A>G rs114713626
NM_001458.4(FLNC):c.-12G>T rs199842696
NM_001458.4(FLNC):c.1032C>T (p.Val344=) rs2291562
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.1614C>T (p.Tyr538=) rs76046880
NM_001458.4(FLNC):c.1814-28T>C rs2291565
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.2122-17T>C rs144828462
NM_001458.4(FLNC):c.2265+12C>G rs2291566
NM_001458.4(FLNC):c.2266-14G>C rs75612085
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.3297A>G (p.Val1099=) rs3734973
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.3838C>T (p.Leu1280=) rs34180031
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.4431G>A (p.Leu1477=) rs2291568
NM_001458.4(FLNC):c.4700G>A (p.Arg1567Gln) rs2291569
NM_001458.4(FLNC):c.4928-7T>C rs201957008
NM_001458.4(FLNC):c.4947C>T (p.Gly1649=) rs201069454
NM_001458.4(FLNC):c.5398+16T>C rs13227216
NM_001458.4(FLNC):c.5592C>T (p.Ala1864=) rs117517372
NM_001458.4(FLNC):c.5669-12C>T rs79790270
NM_001458.4(FLNC):c.5763T>C (p.Thr1921=) rs3816884
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.6459C>T (p.Thr2153=) rs113618587
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.7780+10A>G rs201149834
NM_001458.4(FLNC):c.795T>C (p.Gly265=) rs2291561
NM_001458.4(FLNC):c.850+18G>A rs55907818

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