List of variants in gene FLNB reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 50

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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.6889-18G>A	rs12634123	0.62957
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.2055+274del	rs35415261	0.06556
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.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.669G>A (p.Pro223=)	rs140815373	0.00527
NM_001457.4(FLNB):c.5646G>A (p.Pro1882=)	rs114882667	0.00522
NM_001457.4(FLNB):c.7099G>A (p.Val2367Ile)	rs115747856	0.00488
NM_001457.4(FLNB):c.3078C>T (p.Pro1026=)	rs147267045	0.00465
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.3264C>T (p.Ser1088=)	rs112864468	0.00322
NM_001457.4(FLNB):c.362A>T (p.Tyr121Phe)	rs147846832	0.00269
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.4362G>A (p.Pro1454=)	rs150844992	0.00217
NM_001457.4(FLNB):c.5091C>T (p.Asn1697=)	rs141357606	0.00199
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=)	rs145280904	0.00184
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.4929C>T (p.Ala1643=)	rs149070858	0.00140
NM_001457.4(FLNB):c.6680C>G (p.Ser2227Cys)	rs138327769	0.00050
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.3163G>A (p.Val1055Met)	rs9813235
NM_001457.4(FLNB):c.3724+36del	rs56147140

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