List of variants in gene FLNC reported by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.6889G>A (p.Val2297Met)	rs1420394583	0.00001
NM_001458.5(FLNC):c.2872del (p.Val957_Val958insTer)	rs1401551498
NM_001458.5(FLNC):c.5385dup (p.Gly1796fs)	rs2128938102
NM_001458.5(FLNC):c.8129G>A (p.Trp2710Ter)	rs1585173340
NM_001458.5(FLNC):c.8130G>A (p.Trp2710Ter)	rs121909518

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