List of variants in gene TNNC1 studied for Cardiomyopathy

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_003280.3(TNNC1):c.201C>T (p.Asp67=)	rs150881554	0.00074
NM_003280.3(TNNC1):c.108C>A (p.Ile36=)	rs202000367	0.00030
NM_003280.3(TNNC1):c.210C>T (p.Gly70=)	rs141505676	0.00010
NM_003280.3(TNNC1):c.393C>T (p.Asp131=)	rs147821122	0.00010
NM_003280.3(TNNC1):c.435C>A (p.Asp145Glu)	rs267607124	0.00010
NM_003280.3(TNNC1):c.203-10C>G	rs727505237	0.00002
NM_003280.3(TNNC1):c.216G>A (p.Val72=)	rs770331194	0.00002
NM_003280.3(TNNC1):c.23C>T (p.Ala8Val)	rs267607125	0.00001
NM_003280.3(TNNC1):c.376G>A (p.Glu126Lys)	rs730881060	0.00001
NM_003280.3(TNNC1):c.384C>T (p.Ile128=)	rs1578263808	0.00001
NM_003280.3(TNNC1):c.430A>G (p.Asn144Asp)	rs730881061	0.00001
NM_003280.3(TNNC1):c.439C>T (p.Arg147Cys)	rs796243470	0.00001
NM_003280.3(TNNC1):c.454+7G>A	rs747842576	0.00001
NM_003280.3(TNNC1):c.456G>A (p.Glu152=)	rs568828576	0.00001
NM_003280.3(TNNC1):c.55+9C>A	rs750647348	0.00001
NM_003280.3(TNNC1):c.90C>T (p.Gly30=)	rs149647795	0.00001
NM_003280.3(TNNC1):c.202+9C>T	rs1559616155
NM_003280.3(TNNC1):c.276A>G (p.Lys92=)	rs1578264043
NM_003280.3(TNNC1):c.305G>T (p.Arg102Leu)	rs143020831
NM_003280.3(TNNC1):c.317+8C>A	rs767111898
NM_003280.3(TNNC1):c.417C>T (p.Asp139=)	rs757904305
NM_003280.3(TNNC1):c.433G>C (p.Asp145His)	rs142759728
NM_003280.3(TNNC1):c.486G>T (p.Ter162Tyr)
NM_003280.3(TNNC1):c.73G>A (p.Asp25Asn)	rs730881064

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