ClinVar Miner

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

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.6017A>G (p.Lys2006Arg) rs62621996 0.00994
NM_001457.4(FLNB):c.*1361G>A rs115935959 0.00833
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.669G>A (p.Pro223=) rs140815373 0.00527
NM_001457.4(FLNB):c.5646G>A (p.Pro1882=) rs114882667 0.00522
NM_001457.4(FLNB):c.3785G>C (p.Gly1262Ala) rs111330368 0.00503
NM_001457.4(FLNB):c.7099G>A (p.Val2367Ile) rs115747856 0.00488
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.*732G>A rs75749642 0.00385
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.292+14C>G rs200721532 0.00260
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.1559C>T (p.Pro520Leu) rs138220431 0.00247
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=) rs145280904 0.00184
NM_001457.4(FLNB):c.6244+4T>G rs185737810 0.00178
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.-95C>G rs528555050 0.00150
NM_001457.4(FLNB):c.6741G>A (p.Ser2247=) rs143400214 0.00142
NM_001457.4(FLNB):c.4929C>T (p.Ala1643=) rs149070858 0.00140
NM_001457.4(FLNB):c.3169A>C (p.Lys1057Gln) rs13321615 0.00133
NM_001457.4(FLNB):c.7360G>A (p.Val2454Ile) rs146499414 0.00131
NM_001457.4(FLNB):c.6047G>A (p.Arg2016Gln) rs137885421 0.00117
NM_001457.4(FLNB):c.-97C>T rs150348065 0.00107
NM_001457.4(FLNB):c.2453G>A (p.Arg818Gln) rs151259375 0.00091
NM_001457.4(FLNB):c.1998C>T (p.Ala666=) rs143161769 0.00088
NM_001457.4(FLNB):c.6315C>T (p.Ala2105=) rs147648427 0.00079
NM_001457.4(FLNB):c.4022C>G (p.Ala1341Gly) rs139269734 0.00068
NM_001457.4(FLNB):c.292+12G>C rs201148582 0.00066
NM_001457.4(FLNB):c.6680C>G (p.Ser2227Cys) rs138327769 0.00050
NM_001457.4(FLNB):c.7254C>T (p.Ser2418=) rs563382903 0.00031
NM_001457.4(FLNB):c.5887+8A>G rs143066905 0.00023
NM_001457.4(FLNB):c.3583G>A (p.Val1195Met) rs200993986 0.00021
NM_001457.4(FLNB):c.3430G>C (p.Glu1144Gln) rs199959926 0.00020
NM_001457.4(FLNB):c.*1450G>T rs577715021 0.00019
NM_001457.4(FLNB):c.5769C>T (p.Ala1923=) rs201723447 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
NM_001457.4(FLNB):c.2931G>A (p.Leu977=) rs574484752 0.00012
NM_001457.4(FLNB):c.5532C>T (p.Ile1844=) rs202240037 0.00008
NM_001457.4(FLNB):c.*772C>T rs28364682 0.00004
NM_001457.4(FLNB):c.2935G>A (p.Val979Met) rs376511120 0.00004
NM_001457.4(FLNB):c.1278C>T (p.His426=) rs572259451 0.00003
NM_001457.4(FLNB):c.6829C>T (p.Leu2277=) rs150602768 0.00002
NM_001457.4(FLNB):c.7749G>A (p.Leu2583=) rs535252967 0.00002
NM_001457.4(FLNB):c.5816C>T (p.Thr1939Met) rs372372509 0.00001
NM_001457.4(FLNB):c.6755A>T (p.Tyr2252Phe) rs200567066 0.00001
NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys) rs139875974
NM_001457.4(FLNB):c.3724+36del rs56147140

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