List of variants in gene FLNC reported as likely pathogenic for Cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.4871C>T (p.Ser1624Leu)	rs879255639	0.00003
NM_001458.5(FLNC):c.1549+2T>G	rs111806457
NM_001458.5(FLNC):c.2312del (p.Gly771fs)	rs2536631447
NM_001458.5(FLNC):c.2504dup (p.Pro836fs)	rs1554398705
NM_001458.5(FLNC):c.263del (p.Pro88fs)	rs2536605566
NM_001458.5(FLNC):c.3307_3313del (p.Cys1103fs)	rs2128936386
NM_001458.5(FLNC):c.4288+1G>T	rs2128937065
NM_001458.5(FLNC):c.4702del (p.Asp1568fs)	rs2536648236
NM_001458.5(FLNC):c.5693del (p.Gly1898fs)	rs2536656290
NM_001458.5(FLNC):c.6023dup (p.Glu2009fs)	rs2536659978
NM_001458.5(FLNC):c.6451G>A (p.Gly2151Ser)	rs1563003159
NM_001458.5(FLNC):c.7486del (p.Val2496fs)	rs2536670455

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