List of variants in gene FLNB reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
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.362A>T (p.Tyr121Phe)	rs147846832	0.00269
NM_001457.4(FLNB):c.292+14C>G	rs200721532	0.00260
NM_001457.4(FLNB):c.1472T>C (p.Met491Thr)	rs147575358	0.00203
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=)	rs145280904	0.00184
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.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.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.1461C>T (p.Leu487=)	rs374727625	0.00009
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.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.6078C>T (p.Asp2026=)	rs762010386	0.00001
NM_001457.4(FLNB):c.1327G>C (p.Val443Leu)	rs200902568
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.4515-24GT[4]	rs151085835

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