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
BAP1	gene	BAP1	Expert List;Expert Review Green;NHS GMS	Familial melanoma		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Tumor predisposition syndrome 1, OMIM:614327;{Uveal melanoma, susceptibility to, 2}, OMIM:606661						False	3	100;0;0	2.5	False		ENSG00000163930	ENSG00000163930	HGNC:950													
CDK4	gene	CDK4	Expert List;Expert Review Green;NHS GMS	Familial melanoma		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown							False	3	100;0;0	2.5	False		ENSG00000135446	ENSG00000135446	HGNC:1773													
CDKN2A	gene	CDKN2A	Expert List;Expert Review Green;NHS GMS	Familial melanoma		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Melanoma, cutaneous malignant, 2}, OMIM:155601;{Melanoma and neural system tumor syndrome}, OMIM:155755;{Melanoma-pancreatic cancer syndrome}, OMIM:606719						False	3	100;0;0	2.5	False		ENSG00000147889	ENSG00000147889	HGNC:1787													
POT1	gene	POT1	Expert List;Expert Review Green;NHS GMS	Familial melanoma		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Melanoma, cutaneous malignant, susceptibility to, 10, OMIM:615848				24686849;24686846;29523635;30451293;30586141;32325837;32907878		False	3	67;33;0	2.5	False		ENSG00000128513	ENSG00000128513	HGNC:17284