ClinVar Miner

List of variants in gene FLNB reported as likely pathogenic for not provided

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.572C>T (p.Pro191Leu) rs368472521 0.00005
NM_001457.4(FLNB):c.5110-1G>A rs772444561 0.00002
NC_000003.11:g.(?_58132525)_(58134500_?)del
NM_001457.4(FLNB):c.1346-253_1380del
NM_001457.4(FLNB):c.1610+2_1610+4del
NM_001457.4(FLNB):c.1942-2_1945del
NM_001457.4(FLNB):c.2484+2T>C
NM_001457.4(FLNB):c.2576-2A>T
NM_001457.4(FLNB):c.2745+2T>C rs2107130847
NM_001457.4(FLNB):c.2863+1G>A
NM_001457.4(FLNB):c.292+1G>T
NM_001457.4(FLNB):c.3420del (p.Pro1141fs)
NM_001457.4(FLNB):c.4222+2T>G
NM_001457.4(FLNB):c.4292T>G (p.Leu1431Arg) rs80356511
NM_001457.4(FLNB):c.4390+2T>C
NM_001457.4(FLNB):c.4514+1G>A
NM_001457.4(FLNB):c.4640C>A (p.Ala1547Asp) rs2107220476
NM_001457.4(FLNB):c.4769T>C (p.Ile1590Thr) rs2097315324
NM_001457.4(FLNB):c.4834G>A (p.Gly1612Ser) rs2107225016
NM_001457.4(FLNB):c.4834G>C (p.Gly1612Arg)
NM_001457.4(FLNB):c.4861+2T>C rs2107225089
NM_001457.4(FLNB):c.500A>G (p.Asp167Gly) rs2106946911
NM_001457.4(FLNB):c.501C>A (p.Asp167Glu) rs746892435
NM_001457.4(FLNB):c.5425+1G>A
NM_001457.4(FLNB):c.5454C>A (p.Tyr1818Ter) rs1064796797
NM_001457.4(FLNB):c.605T>C (p.Met202Thr) rs2106952056
NM_001457.4(FLNB):c.622T>G (p.Trp208Gly)
NM_001457.4(FLNB):c.718G>A (p.Ala240Thr) rs2106966046

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