ClinVar Miner

List of variants in gene FLNB reported as benign by Preventiongenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
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.1869C>T (p.Asp623=) rs2140104 0.04479
NM_001457.4(FLNB):c.1611-4G>A rs73074072 0.04164
NM_001457.4(FLNB):c.3857C>T (p.Ala1286Val) rs62621997 0.02930
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.5646G>A (p.Pro1882=) rs114882667 0.00522
NM_001457.4(FLNB):c.3078C>T (p.Pro1026=) rs147267045 0.00465
NM_001457.4(FLNB):c.362A>T (p.Tyr121Phe) rs147846832 0.00269
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.6680C>G (p.Ser2227Cys) rs138327769 0.00050
NM_001457.4(FLNB):c.3163G>A (p.Val1055Met) rs9813235

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.