"PreventionGenetics, part of Exact Sciences"[submitter] AND "TCAP"[gen - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 464946	NM_003673.4(TCAP):c.24C>T (p.Cys8=)	TCAP	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 44707	NM_003673.4(TCAP):c.34GAG[1] (p.Glu13del)	TCAP (E13del)	Microsatellite (inframe_deletion)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 44714	NM_003673.4(TCAP):c.60C>G (p.Ala20=)	TCAP	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 259121	NM_003673.4(TCAP):c.110+7G>A	TCAP	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 259120	NM_003673.4(TCAP):c.110+48C>T	TCAP	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 757231	NM_003673.4(TCAP):c.192G>T (p.Ser64=)	TCAP	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 518961	NM_003673.4(TCAP):c.261G>T (p.Arg87=)	TCAP	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +4 more	GLikely benign
Select item 509098	NM_003673.4(TCAP):c.267G>A (p.Leu89=)	TCAP	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2G +4 more	GLikely benign
Select item 191776	NM_003673.4(TCAP):c.313G>C (p.Glu105Gln)	TCAP (E105Q)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 44706	NM_003673.4(TCAP):c.316C>T (p.Arg106Cys)	TCAP (R106C)	Single nucleotide variant (missense variant)	Primary familial hypertrophic cardiomyopathy +7 more	GBenign/Likely benign
Select item 259122	NM_003673.4(TCAP):c.349C>T (p.Leu117=)	TCAP	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 202105	NM_003673.4(TCAP):c.353C>T (p.Ala118Val)	TCAP (A118V)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 44709	NM_003673.4(TCAP):c.453A>C (p.Ala151=)	TCAP	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +4 more	GBenign