List of variants in gene FLNC reported as pathogenic by GeneDx

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.3791-1G>C	rs781135153	0.00001
NM_001458.5(FLNC):c.1948C>T (p.Arg650Ter)	rs770606675
NM_001458.5(FLNC):c.2084del (p.Arg695fs)	rs1808334682
NM_001458.5(FLNC):c.2119C>T (p.Gln707Ter)	rs1808336992
NM_001458.5(FLNC):c.2234del (p.Gly745fs)	rs1374893890
NM_001458.5(FLNC):c.2390-10_2406del	rs1554398674
NM_001458.5(FLNC):c.3557C>T (p.Ala1186Val)	rs1114167361
NM_001458.5(FLNC):c.4060C>T (p.Arg1354Ter)	rs138193236
NM_001458.5(FLNC):c.4275del (p.Arg1426fs)
NM_001458.5(FLNC):c.554G>A (p.Trp185Ter)	rs1585151331
NM_001458.5(FLNC):c.5704del (p.Ala1902fs)	rs1554400703
NM_001458.5(FLNC):c.6190dup (p.Val2064fs)	rs1808888920
NM_001458.5(FLNC):c.6240_6259del (p.Pro2081fs)	rs2128939085
NM_001458.5(FLNC):c.6976C>T (p.Arg2326Ter)	rs748416758
NM_001458.5(FLNC):c.7371del (p.Glu2458fs)	rs1554401780
NM_001458.5(FLNC):c.805C>T (p.Arg269Ter)	rs755583250

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