ClinVar Miner

List of variants in gene FLNC reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_001458.4(FLNC):c.1082G>A (p.Arg361His) rs752888774
NM_001458.4(FLNC):c.1657G>A (p.Gly553Ser) rs201572079
NM_001458.4(FLNC):c.2293G>A (p.Glu765Lys) rs373798394
NM_001458.4(FLNC):c.2930-5C>T rs371599113
NM_001458.4(FLNC):c.294G>A (p.Glu98=) rs201839252
NM_001458.4(FLNC):c.3242C>T (p.Ala1081Val) rs200169573
NM_001458.4(FLNC):c.3295G>A (p.Val1099Ile) rs759452636
NM_001458.4(FLNC):c.3458T>G (p.Phe1153Cys) rs138663492
NM_001458.4(FLNC):c.3475C>T (p.Arg1159Trp) rs760500171
NM_001458.4(FLNC):c.4296G>A (p.Pro1432=) rs370827536
NM_001458.4(FLNC):c.4880G>A (p.Arg1627His) rs751592993
NM_001458.4(FLNC):c.4991C>T (p.Thr1664Met) rs780829334
NM_001458.4(FLNC):c.5955G>A (p.Ser1985=)
NM_001458.4(FLNC):c.600C>T (p.Pro200=) rs202105410
NM_001458.4(FLNC):c.6817G>A (p.Ala2273Thr) rs372251350

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.