ClinVar Miner

List of variants in gene FLNB reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.4173A>G (p.Ala1391=) rs2362903 0.72429
NM_001457.4(FLNB):c.*1030G>C rs1131264 0.53296
NM_001457.4(FLNB):c.927T>C (p.Ser309=) rs1522384 0.42973
NM_001457.4(FLNB):c.4221C>T (p.Pro1407=) rs2362904 0.42377
NM_001457.4(FLNB):c.4411G>A (p.Val1471Met) rs12632456 0.38984
NM_001457.4(FLNB):c.7359C>T (p.Ser2453=) rs8640 0.36629
NM_001457.4(FLNB):c.3469G>A (p.Asp1157Asn) rs1131356 0.33365
NM_001457.4(FLNB):c.7209G>A (p.Ser2403=) rs13079906 0.09018
NM_001457.4(FLNB):c.*1122T>C rs9613 0.06399
NM_001457.4(FLNB):c.1869C>T (p.Asp623=) rs2140104 0.04479
NM_001457.4(FLNB):c.1611-4G>A rs73074072 0.04164
NM_001457.4(FLNB):c.6438G>A (p.Val2146=) rs60599272 0.03073
NM_001457.4(FLNB):c.3857C>T (p.Ala1286Val) rs62621997 0.02930
NM_001457.4(FLNB):c.792C>T (p.Ile264=) rs7623314 0.02745
NM_001457.4(FLNB):c.3535G>A (p.Glu1179Lys) rs17058845 0.02351
NM_001457.4(FLNB):c.*479G>T rs9880897 0.02305
NM_001457.4(FLNB):c.*200C>T rs9880144 0.02304
NM_001457.4(FLNB):c.*657T>C rs11412 0.02298
NM_001457.4(FLNB):c.*1217G>A rs1131312 0.02294
NM_001457.4(FLNB):c.292+8C>A rs9831243 0.01775
NM_001457.4(FLNB):c.*1370G>A rs1131335 0.01633
NM_001457.4(FLNB):c.4062-5T>G rs3732632 0.01225
NM_001457.4(FLNB):c.*581C>T rs114665501 0.01036
NM_001457.4(FLNB):c.1919C>T (p.Thr640Met) rs62621999 0.00943
NM_001457.4(FLNB):c.-31C>T rs138060096 0.00823
NM_001457.4(FLNB):c.2907G>A (p.Arg969=) rs138449267 0.00724
NM_001457.4(FLNB):c.249G>A (p.Ala83=) rs112750785 0.00622
NM_001457.4(FLNB):c.5426-10G>A rs183917041 0.00264
NM_001457.4(FLNB):c.5091C>T (p.Asn1697=) rs141357606 0.00199
NM_001457.4(FLNB):c.7183G>A (p.Glu2395Lys) rs142023538 0.00019
NM_001457.4(FLNB):c.6416G>A (p.Arg2139His) rs578244438 0.00010
NM_001457.4(FLNB):c.1946G>A (p.Arg649Gln) rs145910735 0.00006
NM_001457.4(FLNB):c.*675G>A rs372717760 0.00002
NM_001457.4(FLNB):c.*592C>G rs11667

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