ClinVar Miner

List of variants in gene FLNC reported by Genetic Services Laboratory, University of Chicago

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Total variants: 26
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HGVS dbSNP
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.1458C>A (p.Pro486=) rs2291563
NM_001458.4(FLNC):c.147C>T (p.His49=) rs3734972
NM_001458.4(FLNC):c.1614C>T (p.Tyr538=) rs76046880
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.3757G>A (p.Val1253Ile) rs117366477
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.5377G>A (p.Val1793Met) rs587780337
NM_001458.4(FLNC):c.5592C>T (p.Ala1864=) rs117517372
NM_001458.4(FLNC):c.5763T>C (p.Thr1921=) rs3816884
NM_001458.4(FLNC):c.5805G>A (p.Lys1935=) rs759262897
NM_001458.4(FLNC):c.6771A>G (p.Pro2257=) rs34422412
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.8003T>C (p.Met2668Thr) rs200502811
NM_001458.4(FLNC):c.8118C>T (p.Leu2706=) rs28379666
NM_001458.4(FLNC):c.8121T>C (p.Ile2707=) rs28437296

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