List of variants in gene TNNI3 reported by Agnes Ginges Centre for Molecular Cardiology, Centenary Institute

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp)	rs368861241	0.00004
NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln)	rs397516349	0.00002
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln)	rs727503506	0.00001
NM_000363.5(TNNI3):c.433C>T (p.Arg145Trp)	rs104894724	0.00001
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln)	rs397516354	0.00001
NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe)	rs773216333
NM_000363.5(TNNI3):c.440T>C (p.Val147Ala)	rs2085712229
NM_000363.5(TNNI3):c.496T>C (p.Ser166Pro)	rs1599909123
NM_000363.5(TNNI3):c.500T>C (p.Leu167Pro)	rs1391407750
NM_000363.5(TNNI3):c.538G>A (p.Asp180Asn)	rs1060503103
NM_000363.5(TNNI3):c.550-1G>A	rs1555863017
NM_000363.5(TNNI3):c.611G>A (p.Arg204His)	rs727504275

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