ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.3469G>A (p.Asp1157Asn) rs1131356 0.33365
NM_001457.4(FLNB):c.2055+274del rs35415261 0.06556
NM_001457.4(FLNB):c.1611-4G>A rs73074072 0.04164
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.292+8C>A rs9831243 0.01775
NM_001457.4(FLNB):c.4062-5T>G rs3732632 0.01225
NM_001457.4(FLNB):c.6017A>G (p.Lys2006Arg) rs62621996 0.00994
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.3771G>A (p.Pro1257=) rs146851485 0.00794
NM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr) rs116826041 0.00739
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.720C>T (p.Ala240=) rs111433950 0.00554
NM_001457.4(FLNB):c.5646G>A (p.Pro1882=) rs114882667 0.00522
NM_001457.4(FLNB):c.3078C>T (p.Pro1026=) rs147267045 0.00465
NM_001457.4(FLNB):c.4671+11G>A rs115346578 0.00454
NM_001457.4(FLNB):c.4872C>T (p.Ile1624=) rs147426569 0.00436
NM_001457.4(FLNB):c.3090C>T (p.Tyr1030=) rs112968165 0.00406
NM_001457.4(FLNB):c.2382C>T (p.Asp794=) rs146159035 0.00360
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=) rs77989135 0.00333
NM_001457.4(FLNB):c.3264C>T (p.Ser1088=) rs112864468 0.00322
NM_001457.4(FLNB):c.4222+19A>C rs146229370 0.00319
NM_001457.4(FLNB):c.5426-10G>A rs183917041 0.00264
NM_001457.4(FLNB):c.1044C>T (p.Asp348=) rs111996979 0.00252
NM_001457.4(FLNB):c.4222+8A>G rs190025781 0.00248
NM_001457.4(FLNB):c.4377T>C (p.Val1459=) rs149921907 0.00232
NM_001457.4(FLNB):c.274A>G (p.Ile92Val) rs62622011 0.00229
NM_001457.4(FLNB):c.4362G>A (p.Pro1454=) rs150844992 0.00217
NM_001457.4(FLNB):c.5091C>T (p.Asn1697=) rs141357606 0.00199
NM_001457.4(FLNB):c.6684C>T (p.Ile2228=) rs138416613 0.00170
NM_001457.4(FLNB):c.6642C>T (p.Phe2214=) rs140786324 0.00161
NM_001457.4(FLNB):c.6773-13C>A rs200653965 0.00149
NM_001457.4(FLNB):c.5769C>T (p.Ala1923=) rs201723447 0.00019
NM_001457.4(FLNB):c.7198+20C>G rs201580886 0.00019
NM_001457.4(FLNB):c.4390+8T>A rs377095569 0.00018
NM_001457.4(FLNB):c.5785G>A (p.Asp1929Asn) rs146685642 0.00017

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