ClinVar Miner

List of variants in gene FLNC reported as benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP
NM_001458.4(FLNC):c.1425C>T (p.Asn475=) rs143610360
NM_001458.4(FLNC):c.1577G>A (p.Arg526Gln) rs34932223
NM_001458.4(FLNC):c.1902G>A (p.Glu634=) rs12536635
NM_001458.4(FLNC):c.2078A>C (p.Asp693Ala) rs34972246
NM_001458.4(FLNC):c.2501C>T (p.Thr834Met) rs75133741
NM_001458.4(FLNC):c.3006G>A (p.Arg1002=) rs61737781
NM_001458.4(FLNC):c.3506A>G (p.Lys1169Arg) rs530742766
NM_001458.4(FLNC):c.3721C>T (p.Arg1241Cys) rs146953558
NM_001458.4(FLNC):c.3973C>T (p.Leu1325=) rs34373805
NM_001458.4(FLNC):c.4289-4A>C rs140031589
NM_001458.4(FLNC):c.4404C= (p.Asp1468=) rs2249128
NM_001458.4(FLNC):c.4431G>A (p.Leu1477=) rs2291568
NM_001458.4(FLNC):c.4737+9_4737+10delCT rs794727437
NM_001458.4(FLNC):c.4928-7T>C rs201957008
NM_001458.4(FLNC):c.5042C>G (p.Thr1681Arg) rs193159707
NM_001458.4(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717
NM_001458.4(FLNC):c.5592C>T (p.Ala1864=) rs117517372
NM_001458.4(FLNC):c.5763T>C (p.Thr1921=) rs3816884
NM_001458.4(FLNC):c.5764G>A (p.Ala1922Thr) rs202128602
NM_001458.4(FLNC):c.597C>T (p.Ala199=) rs143942649
NM_001458.4(FLNC):c.6005-9T>C rs118124743
NM_001458.4(FLNC):c.6459C>T (p.Thr2153=) rs113618587
NM_001458.4(FLNC):c.7091G>A (p.Arg2364His) rs201672146

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.