ClinVar Miner

List of variants in gene FLNB reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.2453G>A (p.Arg818Gln) rs151259375 0.00091
NM_001457.4(FLNB):c.4058C>G (p.Thr1353Ser) rs142718547 0.00043
NM_001457.4(FLNB):c.6515G>A (p.Arg2172His) rs139846706 0.00034
NM_001457.4(FLNB):c.2644G>C (p.Val882Leu) rs139124254 0.00019
NM_001457.4(FLNB):c.2095C>T (p.Arg699Trp) rs200554477 0.00015
NM_001457.4(FLNB):c.1640C>T (p.Ala547Val) rs200619215 0.00012
NM_001457.4(FLNB):c.1216G>A (p.Val406Met) rs367842487 0.00007
NM_001457.4(FLNB):c.6221A>G (p.Lys2074Arg) rs148043654 0.00007
NM_001457.4(FLNB):c.2968C>T (p.Pro990Ser) rs747564760 0.00006
NM_001457.4(FLNB):c.7690G>A (p.Val2564Ile) rs759652781 0.00006
NM_001457.4(FLNB):c.2096G>A (p.Arg699Gln) rs752842243 0.00005
NM_001457.4(FLNB):c.2965G>A (p.Val989Met) rs76471260 0.00005
NM_001457.4(FLNB):c.1135A>G (p.Ile379Val) rs374118649 0.00004
NM_001457.4(FLNB):c.2005A>G (p.Thr669Ala) rs147481678 0.00003
NM_001457.4(FLNB):c.5147C>T (p.Pro1716Leu) rs201370865 0.00003
NM_001457.4(FLNB):c.1628T>C (p.Val543Ala) rs773177128 0.00002
NM_001457.4(FLNB):c.1897A>G (p.Met633Val) rs937051879 0.00002
NM_001457.4(FLNB):c.1808C>T (p.Ser603Leu) rs764538938 0.00001
NM_001457.4(FLNB):c.2356C>T (p.Arg786Trp) rs201452322 0.00001
NM_001457.4(FLNB):c.2744A>G (p.Gln915Arg) rs771989645 0.00001
NM_001457.4(FLNB):c.4717G>A (p.Asp1573Asn) rs373528171 0.00001
NM_001457.4(FLNB):c.4774G>A (p.Val1592Ile) rs754360853 0.00001
NM_001457.4(FLNB):c.6211G>A (p.Val2071Ile) rs201831615 0.00001
NM_001457.4(FLNB):c.107G>A (p.Arg36His) rs142568031
NM_001457.4(FLNB):c.1748-6C>G rs2097260334
NM_001457.4(FLNB):c.2642A>G (p.Asn881Ser) rs1199239072
NM_001457.4(FLNB):c.4402C>T (p.Pro1468Ser) rs988254831
NM_001457.4(FLNB):c.4411G>C (p.Val1471Leu) rs12632456

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