List of variants in gene FLNB reported as uncertain significance by Eurofins NTD LLC (GA)

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.6000T>C (p.Gly2000=)	rs140926445	0.00127
NM_001457.4(FLNB):c.6047G>A (p.Arg2016Gln)	rs137885421	0.00117
NM_001457.4(FLNB):c.808A>G (p.Met270Val)	rs145036794	0.00096
NM_001457.4(FLNB):c.3288C>T (p.Ser1096=)	rs77934864	0.00071
NM_001457.4(FLNB):c.4307G>A (p.Arg1436Gln)	rs140018418	0.00067
NM_001457.4(FLNB):c.6843C>T (p.Ile2281=)	rs140332932	0.00062
NM_001457.4(FLNB):c.4040A>G (p.Asn1347Ser)	rs146093652	0.00056
NM_001457.4(FLNB):c.6173A>G (p.Lys2058Arg)	rs141698427	0.00048
NM_001457.4(FLNB):c.4058C>G (p.Thr1353Ser)	rs142718547	0.00043
NM_001457.4(FLNB):c.4061+4G>A	rs370061963	0.00032
NM_001457.4(FLNB):c.7254C>T (p.Ser2418=)	rs563382903	0.00031
NM_001457.4(FLNB):c.3594G>A (p.Thr1198=)	rs143566075	0.00024
NM_001457.4(FLNB):c.3967A>T (p.Thr1323Ser)	rs202156074	0.00013
NM_001457.4(FLNB):c.1303G>A (p.Asp435Asn)	rs781162510	0.00006
NM_001457.4(FLNB):c.1946G>A (p.Arg649Gln)	rs145910735	0.00006
NM_001457.4(FLNB):c.2965G>A (p.Val989Met)	rs76471260	0.00005
NM_001457.4(FLNB):c.6003C>T (p.Asp2001=)	rs184065600	0.00004
NM_001457.4(FLNB):c.3826G>T (p.Ala1276Ser)	rs199912711	0.00003
NM_001457.4(FLNB):c.6154C>T (p.Leu2052=)	rs372726521	0.00003
NM_001457.4(FLNB):c.6497C>T (p.Thr2166Met)	rs199939739	0.00002
NM_001457.4(FLNB):c.1212G>A (p.Leu404=)	rs150637036	0.00001
NM_001457.4(FLNB):c.1346C>T (p.Ala449Val)	rs1441992629	0.00001
NM_001457.4(FLNB):c.2586T>G (p.Asn862Lys)	rs750635182	0.00001
NM_001457.4(FLNB):c.2654A>G (p.Asn885Ser)	rs886042526	0.00001
NM_001457.4(FLNB):c.3144C>T (p.Pro1048=)	rs376519914	0.00001
NM_001457.4(FLNB):c.5043G>A (p.Pro1681=)	rs886042162	0.00001
NM_001457.4(FLNB):c.871G>A (p.Val291Met)	rs751747906	0.00001
NM_001457.4(FLNB):c.1082G>T (p.Gly361Val)	rs794727854
NM_001457.4(FLNB):c.3163G>T (p.Val1055Leu)	rs9813235
NM_001457.4(FLNB):c.4391G>C (p.Gly1464Ala)	rs886044175
NM_001457.4(FLNB):c.492C>G (p.Asn164Lys)	rs886042790
NM_001457.4(FLNB):c.5967C>T (p.Pro1989=)	rs374686904
NM_001457.4(FLNB):c.6367+7G>C	rs201871482
NM_001457.4(FLNB):c.7301C>T (p.Thr2434Ile)	rs748246153

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