List of variants in gene TCAP 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003673.4(TCAP):c.316C>T (p.Arg106Cys)	rs45578741	0.00813
NM_003673.4(TCAP):c.191C>T (p.Ser64Leu)	rs45458802	0.00421
NM_003673.4(TCAP):c.32C>T (p.Ser11Leu)	rs45495192	0.00113
NM_003673.4(TCAP):c.353C>T (p.Ala118Val)	rs143233087	0.00092
NM_003673.4(TCAP):c.313G>C (p.Glu105Gln)	rs146906267	0.00051
NM_003673.4(TCAP):c.388C>T (p.Arg130Cys)	rs374886575	0.00009
NM_003673.4(TCAP):c.132C>T (p.Asp44=)	rs397516861	0.00006
NM_003673.4(TCAP):c.480G>A (p.Met160Ile)	rs755395354	0.00006
NM_003673.4(TCAP):c.460C>T (p.Arg154Cys)	rs755539784	0.00004
NM_003673.4(TCAP):c.421C>G (p.Pro141Ala)	rs45509691	0.00002
NM_003673.4(TCAP):c.34GAG[1] (p.Glu13del)	rs397516862
NM_003673.4(TCAP):c.453_470del (p.Leu152_Ser157del)	rs749817987
NM_003673.4(TCAP):c.472C>T (p.Arg158Cys)	rs397516863
NM_003673.4(TCAP):c.494A>T (p.Gln165Leu)	rs2057253901

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