ClinVar Miner

List of variants in gene FLNB reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 35
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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.4872C>T (p.Ile1624=) rs147426569 0.00436
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=) rs77989135 0.00333
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.4377T>C (p.Val1459=) rs149921907 0.00232
NM_001457.4(FLNB):c.4362G>A (p.Pro1454=) rs150844992 0.00217
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.6741G>A (p.Ser2247=) rs143400214 0.00142
NM_001457.4(FLNB):c.4929C>T (p.Ala1643=) rs149070858 0.00140
NM_001457.4(FLNB):c.420G>A (p.Thr140=) rs192491895 0.00134
NM_001457.4(FLNB):c.7360G>A (p.Val2454Ile) rs146499414 0.00131
NM_001457.4(FLNB):c.7668C>T (p.Cys2556=) rs144621434 0.00125
NM_001457.4(FLNB):c.3522G>A (p.Ser1174=) rs140993979 0.00111
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.4391-825T>C rs142631042 0.00065
NM_001457.4(FLNB):c.7254C>T (p.Ser2418=) rs563382903 0.00031
NM_001457.4(FLNB):c.7255G>A (p.Val2419Ile) rs202143851 0.00024
NM_001457.4(FLNB):c.5887+8A>G rs143066905 0.00023
NM_001457.4(FLNB):c.1534G>A (p.Ala512Thr) rs201544295 0.00022
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.5220C>T (p.Asn1740=) rs531970315 0.00008
NM_001457.4(FLNB):c.1278C>T (p.His426=) rs572259451 0.00003
NM_001457.4(FLNB):c.5816C>T (p.Thr1939Met) rs372372509 0.00001
NM_001457.4(FLNB):c.6333C>T (p.Val2111=) rs532229449 0.00001
NC_000003.12:g.58179951G>A
NM_001457.4(FLNB):c.1128C>T (p.Tyr376=)
NM_001457.4(FLNB):c.1143G>A (p.Thr381=)
NM_001457.4(FLNB):c.3351C>T (p.His1117=)
NM_001457.4(FLNB):c.4391-877C>T
NM_001457.4(FLNB):c.7125T>C (p.Val2375=)

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