List of variants in gene TCAP reported by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003673.4(TCAP):c.453A>C (p.Ala151=)	rs1053651	0.61044
NM_003673.4(TCAP):c.110+48C>T	rs2941510	0.05382
NM_003673.4(TCAP):c.316C>T (p.Arg106Cys)	rs45578741	0.00813
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.60C>G (p.Ala20=)	rs146502276	0.00034
NM_003673.4(TCAP):c.261G>T (p.Arg87=)	rs375389509	0.00003
NM_003673.4(TCAP):c.267G>A (p.Leu89=)	rs1419129039	0.00002
NM_003673.4(TCAP):c.24C>T (p.Cys8=)	rs756548785	0.00001
NM_003673.4(TCAP):c.110+7G>A	rs886038533
NM_003673.4(TCAP):c.192G>T (p.Ser64=)	rs771585295
NM_003673.4(TCAP):c.349C>T (p.Leu117=)	rs886038534
NM_003673.4(TCAP):c.34GAG[1] (p.Glu13del)	rs397516862

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