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
POT1	gene	POT1	Expert Review Green;NHS GMS	Li Fraumeni Syndrome		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Tumor predisposition syndrome 3, OMIM:615848;?Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8, OMIM:620367;tumor predisposition syndrome 3, MONDO:0014368						False	3	100;0;0	1.6	False		ENSG00000128513	ENSG00000128513	HGNC:17284													
TP53	gene	TP53	Expert Review Green;NHS GMS	Li Fraumeni Syndrome		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Li-Fraumeni syndrome, OMIM:151623;Li-Fraumeni syndrome, MONDO:0018875						False	3	0;0;0	1.6	False		ENSG00000141510	ENSG00000141510	HGNC:11998