ClinVar Miner

List of variants in gene FLNC reported as uncertain significance for Inborn genetic diseases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.3304C>T (p.Pro1102Ser) rs199707920 0.00015
NM_001458.5(FLNC):c.2419C>T (p.Pro807Ser) rs946201226 0.00007
NM_001458.5(FLNC):c.5945G>A (p.Arg1982His) rs375046429 0.00004
NM_001458.5(FLNC):c.4911C>G (p.Ser1637Arg) rs1469272964 0.00003
NM_001458.5(FLNC):c.1169A>G (p.Asn390Ser) rs188905854 0.00001
NM_001458.5(FLNC):c.1216G>A (p.Gly406Ser) rs1343684536 0.00001
NM_001458.5(FLNC):c.1771G>A (p.Asp591Asn) rs768829742 0.00001
NM_001458.5(FLNC):c.2287C>T (p.His763Tyr) rs1380984220 0.00001
NM_001458.5(FLNC):c.3268G>T (p.Ala1090Ser) rs760158891 0.00001
NM_001458.5(FLNC):c.4172C>T (p.Ser1391Leu) rs755832014 0.00001
NM_001458.5(FLNC):c.4474G>A (p.Glu1492Lys) rs71581926 0.00001
NM_001458.5(FLNC):c.6572C>T (p.Thr2191Met) rs768329311 0.00001
NM_001458.5(FLNC):c.7328G>A (p.Arg2443Gln) rs370293647 0.00001
NM_001458.5(FLNC):c.7580T>C (p.Ile2527Thr) rs749891076 0.00001
NM_001458.5(FLNC):c.1175C>A (p.Ala392Asp) rs1808189981
NM_001458.5(FLNC):c.1445G>A (p.Arg482Gln) rs770337434
NM_001458.5(FLNC):c.1903C>T (p.Pro635Ser)
NM_001458.5(FLNC):c.2230T>C (p.Trp744Arg)
NM_001458.5(FLNC):c.2377G>C (p.Glu793Gln)
NM_001458.5(FLNC):c.2461A>G (p.Ile821Val)
NM_001458.5(FLNC):c.3178C>G (p.Pro1060Ala) rs2128936236
NM_001458.5(FLNC):c.3212G>C (p.Gly1071Ala)
NM_001458.5(FLNC):c.3286G>A (p.Gly1096Arg)
NM_001458.5(FLNC):c.3499C>A (p.Arg1167Ser)
NM_001458.5(FLNC):c.3739G>A (p.Ala1247Thr)
NM_001458.5(FLNC):c.3857A>C (p.Asn1286Thr)
NM_001458.5(FLNC):c.3983T>C (p.Val1328Ala)
NM_001458.5(FLNC):c.4280C>T (p.Pro1427Leu) rs1192906461
NM_001458.5(FLNC):c.4857T>G (p.Asp1619Glu)
NM_001458.5(FLNC):c.5175C>G (p.Ile1725Met)
NM_001458.5(FLNC):c.5413C>T (p.Pro1805Ser) rs1808775264
NM_001458.5(FLNC):c.5672G>C (p.Gly1891Ala)
NM_001458.5(FLNC):c.5994C>A (p.Asn1998Lys)
NM_001458.5(FLNC):c.6273G>C (p.Met2091Ile)
NM_001458.5(FLNC):c.6340T>C (p.Phe2114Leu)
NM_001458.5(FLNC):c.6656C>T (p.Pro2219Leu)
NM_001458.5(FLNC):c.6658G>T (p.Ala2220Ser)
NM_001458.5(FLNC):c.7176C>G (p.Ile2392Met) rs1585170543
NM_001458.5(FLNC):c.7319T>C (p.Ile2440Thr) rs764628080
NM_001458.5(FLNC):c.869A>G (p.Asn290Ser)
NM_001458.5(FLNC):c.914C>T (p.Ala305Val)

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.