List of variants in gene FLNC reported as likely benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.2266-14G>C	rs75612085	0.01030
NM_001458.5(FLNC):c.3721C>T (p.Arg1241Cys)	rs146953558	0.00728
NM_001458.5(FLNC):c.2078A>C (p.Asp693Ala)	rs34972246	0.00297
NM_001458.5(FLNC):c.4928-7T>C	rs201957008	0.00286
NM_001458.5(FLNC):c.561C>T (p.Asp187=)	rs149474376	0.00178
NM_001458.5(FLNC):c.2390-9T>C	rs368068407	0.00168
NM_001458.5(FLNC):c.5644A>G (p.Ile1882Val)	rs184018403	0.00160
NM_001458.5(FLNC):c.2389+12C>T	rs370526829	0.00151
NM_001458.5(FLNC):c.1813+11G>T	rs138716837	0.00126
NM_001458.5(FLNC):c.597C>T (p.Ala199=)	rs143942649	0.00124
NM_001458.5(FLNC):c.5418G>A (p.Ser1806=)	rs376078394	0.00090
NM_001458.5(FLNC):c.7990+9C>T	rs566679569	0.00077
NM_001458.5(FLNC):c.6175G>A (p.Val2059Met)	rs201333104	0.00076
NM_001458.5(FLNC):c.1519G>A (p.Gly507Arg)	rs189525930	0.00060
NM_001458.5(FLNC):c.6120C>T (p.Asp2040=)	rs116974302	0.00039
NM_001458.5(FLNC):c.7991-19C>T	rs537052947	0.00034
NM_001458.5(FLNC):c.294G>A (p.Glu98=)	rs201839252	0.00029
NM_001458.5(FLNC):c.2733G>A (p.Lys911=)	rs374135903	0.00024
NM_001458.5(FLNC):c.1434C>T (p.Arg478=)	rs201810745	0.00023
NM_001458.5(FLNC):c.6888C>T (p.His2296=)	rs375259002	0.00017
NM_001458.5(FLNC):c.4153C>T (p.Leu1385=)	rs202125701	0.00016
NM_001458.5(FLNC):c.3153G>A (p.Pro1051=)	rs373694043	0.00015
NM_001458.5(FLNC):c.6594C>T (p.Gly2198=)	rs754112206	0.00014
NM_001458.5(FLNC):c.600C>T (p.Pro200=)	rs202105410	0.00013
NM_001458.5(FLNC):c.4914G>A (p.Lys1638=)	rs371385321	0.00009
NM_001458.5(FLNC):c.4488T>C (p.Asn1496=)	rs377258966	0.00008
NM_001458.5(FLNC):c.2490C>T (p.Thr830=)	rs777580254	0.00005
NM_001458.5(FLNC):c.6864C>T (p.Val2288=)	rs761269440	0.00004
NM_001458.5(FLNC):c.5273G>A (p.Arg1758Gln)	rs573984029	0.00003
NM_001458.5(FLNC):c.602-16T>A	rs1236096502	0.00003
NM_001458.5(FLNC):c.3372G>A (p.Thr1124=)	rs556913973	0.00002
NM_001458.5(FLNC):c.558G>A (p.Gln186=)	rs532206394	0.00002
NM_001458.5(FLNC):c.2982C>T (p.Gly994=)	rs947174901	0.00001
NM_001458.5(FLNC):c.4134G>A (p.Ala1378=)	rs200942470	0.00001
NM_001458.5(FLNC):c.4728C>T (p.Val1576=)	rs1222823077	0.00001
NM_001458.5(FLNC):c.5281G>A (p.Ala1761Thr)	rs376023896	0.00001
NM_001458.5(FLNC):c.-26_-9dup	rs749265933
NM_001458.5(FLNC):c.4812G>A (p.Pro1604=)	rs553400393

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