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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 99

Download table as spreadsheet

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.3785G>C (p.Gly1262Ala)	rs111330368	0.00503
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.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.362A>T (p.Tyr121Phe)	rs147846832	0.00269
NM_001457.4(FLNB):c.5426-10G>A	rs183917041	0.00264
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.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.1472T>C (p.Met491Thr)	rs147575358	0.00203
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.6773-13C>A	rs200653965	0.00149
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.3522G>A (p.Ser1174=)	rs140993979	0.00111
NM_001457.4(FLNB):c.2453G>A (p.Arg818Gln)	rs151259375	0.00091
NM_001457.4(FLNB):c.3288C>T (p.Ser1096=)	rs77934864	0.00071
NM_001457.4(FLNB):c.4022C>G (p.Ala1341Gly)	rs139269734	0.00068
NM_001457.4(FLNB):c.4233C>G (p.Phe1411Leu)	rs143831841	0.00066
NM_001457.4(FLNB):c.1196A>G (p.Lys399Arg)	rs145673747	0.00043
NM_001457.4(FLNB):c.4058C>G (p.Thr1353Ser)	rs142718547	0.00043
NM_001457.4(FLNB):c.6515G>A (p.Arg2172His)	rs139846706	0.00034
NM_001457.4(FLNB):c.3981G>A (p.Gln1327=)	rs201441533	0.00033
NM_001457.4(FLNB):c.4061+4G>A	rs370061963	0.00032
NM_001457.4(FLNB):c.3594G>A (p.Thr1198=)	rs143566075	0.00024
NM_001457.4(FLNB):c.3898+19G>A	rs780062399	0.00021
NM_001457.4(FLNB):c.5407A>T (p.Met1803Leu)	rs200677473	0.00021
NM_001457.4(FLNB):c.2644G>C (p.Val882Leu)	rs139124254	0.00019
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
NM_001457.4(FLNB):c.2095C>T (p.Arg699Trp)	rs200554477	0.00015
NM_001457.4(FLNB):c.1640C>T (p.Ala547Val)	rs200619215	0.00012
NM_001457.4(FLNB):c.1461C>T (p.Leu487=)	rs374727625	0.00009
NM_001457.4(FLNB):c.1216G>A (p.Val406Met)	rs367842487	0.00007
NM_001457.4(FLNB):c.1873G>A (p.Glu625Lys)	rs372998485	0.00007
NM_001457.4(FLNB):c.4449C>T (p.Tyr1483=)	rs118012972	0.00007
NM_001457.4(FLNB):c.6221A>G (p.Lys2074Arg)	rs148043654	0.00007
NM_001457.4(FLNB):c.2968C>T (p.Pro990Ser)	rs747564760	0.00006
NM_001457.4(FLNB):c.7690G>A (p.Val2564Ile)	rs759652781	0.00006
NM_001457.4(FLNB):c.2096G>A (p.Arg699Gln)	rs752842243	0.00005
NM_001457.4(FLNB):c.2965G>A (p.Val989Met)	rs76471260	0.00005
NM_001457.4(FLNB):c.1135A>G (p.Ile379Val)	rs374118649	0.00004
NM_001457.4(FLNB):c.2005A>G (p.Thr669Ala)	rs147481678	0.00003
NM_001457.4(FLNB):c.5147C>T (p.Pro1716Leu)	rs201370865	0.00003
NM_001457.4(FLNB):c.1628T>C (p.Val543Ala)	rs773177128	0.00002
NM_001457.4(FLNB):c.1897A>G (p.Met633Val)	rs937051879	0.00002
NM_001457.4(FLNB):c.246G>C (p.Val82=)	rs780155723	0.00002
NM_001457.4(FLNB):c.2484+19G>A	rs765081115	0.00002
NM_001457.4(FLNB):c.3189C>T (p.Ile1063=)	rs769902031	0.00002
NM_001457.4(FLNB):c.1808C>T (p.Ser603Leu)	rs764538938	0.00001
NM_001457.4(FLNB):c.2356C>T (p.Arg786Trp)	rs201452322	0.00001
NM_001457.4(FLNB):c.2744A>G (p.Gln915Arg)	rs771989645	0.00001
NM_001457.4(FLNB):c.4717G>A (p.Asp1573Asn)	rs373528171	0.00001
NM_001457.4(FLNB):c.4774G>A (p.Val1592Ile)	rs754360853	0.00001
NM_001457.4(FLNB):c.6078C>T (p.Asp2026=)	rs762010386	0.00001
NM_001457.4(FLNB):c.6211G>A (p.Val2071Ile)	rs201831615	0.00001
NM_001457.4(FLNB):c.107G>A (p.Arg36His)	rs142568031
NM_001457.4(FLNB):c.1327G>C (p.Val443Leu)	rs200902568
NM_001457.4(FLNB):c.1748-6C>G	rs2097260334
NM_001457.4(FLNB):c.2251G>C (p.Gly751Arg)	rs28937587
NM_001457.4(FLNB):c.2642A>G (p.Asn881Ser)	rs1199239072
NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys)	rs139875974
NM_001457.4(FLNB):c.3163G>A (p.Val1055Met)	rs9813235
NM_001457.4(FLNB):c.4191T>G (p.Val1397=)
NM_001457.4(FLNB):c.4402C>T (p.Pro1468Ser)	rs988254831
NM_001457.4(FLNB):c.4411G>C (p.Val1471Leu)	rs12632456
NM_001457.4(FLNB):c.4515-24GT[4]	rs151085835
NM_001457.4(FLNB):c.502G>T (p.Gly168Cys)	rs80356504

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.