Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
CALM1	gene	CALM1	Expert Review Green;Victorian Clinical Genetics Services	Catecholaminergic Polymorphic Ventricular Tachycardia		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Long QT syndrome 14	616247;Ventricular tachycardia, catecholaminergic polymorphic, 4	614916"				31170290		False	3	100;0;0	0.35	True		ENSG00000198668	ENSG00000198668	HGNC:1442													
CALM2	gene	CALM2	Expert Review Green;Victorian Clinical Genetics Services	Catecholaminergic Polymorphic Ventricular Tachycardia		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Long QT syndrome 15	616249;sudden unexplained death;idopathic VF"				31170290		False	3	0;0;0	0.35	True		ENSG00000143933	ENSG00000143933	HGNC:1445													
CASQ2	gene	CASQ2	Expert Review Green;Victorian Clinical Genetics Services	Catecholaminergic Polymorphic Ventricular Tachycardia		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	"Ventricular tachycardia, catecholaminergic polymorphic, 2, MIM#	611938"				16908766;11704930		False	3	100;0;0	0.35	True		ENSG00000118729	ENSG00000118729	HGNC:1513													
RYR2	gene	RYR2	Expert Review Green;Victorian Clinical Genetics Services	Catecholaminergic Polymorphic Ventricular Tachycardia		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Ventricular tachycardia, catecholaminergic polymorphic, 1 604772						False	3	100;0;0	0.35	True		ENSG00000198626	ENSG00000198626	HGNC:10484													
TECRL	gene	TECRL	Expert Review Green;Literature	Catecholaminergic Polymorphic Ventricular Tachycardia		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	"Ventricular tachycardia, catecholaminergic polymorphic, 3, MIM#	614021"				17666061;27861123;30790670;33367594		False	3	100;0;0	0.35	True		ENSG00000205678	ENSG00000205678	HGNC:27365													
TRDN	gene	TRDN	Expert Review Green;Victorian Clinical Genetics Services	Catecholaminergic Polymorphic Ventricular Tachycardia		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Triadin knockout syndrome;CPVT;atypical LQTS phenotype				30649896;25922419;22422768		False	3	100;0;0	0.35	True		ENSG00000186439	ENSG00000186439	HGNC:12261