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
PTCH1	gene	PTCH1	Expert Review Green;NHS GMS	Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Basal cell nevus syndrome 1, OMIM:109400;basal cell nevus syndrome 1, MONDO:0958174						False	3	100;0;0	1.4	False		ENSG00000185920	ENSG00000185920	HGNC:9585													
SUFU	gene	SUFU	Expert Review Green;NHS GMS	Nevoid Basal Cell Carcinoma Syndrome or Gorlin syndrome		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Basal cell nevus syndrome 2, OMIM:620343;basal cell nevus syndrome 2, MONDO:0958189						False	3	100;0;0	1.4	False		ENSG00000107882	ENSG00000107882	HGNC:16466