C4225408[trait identifier] AND "Mayo Clinic Laboratories, Mayo Clinic" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 263956	NM_003673.4(TCAP):c.52C>T (p.Arg18Trp)	TCAP (R18W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 202108	NM_003673.4(TCAP):c.113G>T (p.Cys38Phe)	TCAP (C38F)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +6 more	GConflicting classifications of pathogenicity
Select item 520315	NM_003673.4(TCAP):c.202A>T (p.Met68Leu)	TCAP (M68L)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 191776	NM_003673.4(TCAP):c.313G>C (p.Glu105Gln)	TCAP (E105Q)	Single nucleotide variant (missense variant)	Primary familial hypertrophic cardiomyopathy +7 more	GConflicting classifications of pathogenicity
Select item 202104	NM_003673.4(TCAP):c.334C>T (p.Gln112Ter)	TCAP (Q112*)	Single nucleotide variant (nonsense)	Primary familial hypertrophic cardiomyopathy +3 more	GConflicting classifications of pathogenicity
Select item 430120	NM_003673.4(TCAP):c.480G>A (p.Met160Ile)	TCAP (M160I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GUncertain significance

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