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
MSH6	gene	MSH6	Expert list;Expert Review Amber	Multiple monogenic benign skin tumours		Dermatology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Muir-Torre syndrome, MONDO:0008018						False	2	0;100;0	2.5	False		ENSG00000116062	ENSG00000116062	HGNC:7329													
NOTCH3	gene	NOTCH3	Expert Review Amber;Other	Multiple monogenic benign skin tumours		Dermatology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	?Myofibromatosis, infantile 2, OMIM:615293;myofibromatosis, infantile, 2, MONDO:0014122				33509954;23731542		False	2	0;100;0	2.5	False		ENSG00000074181	ENSG00000074181	HGNC:7883													
PMS2	gene	PMS2	Expert list;Expert Review Amber	Multiple monogenic benign skin tumours		Dermatology	BIALLELIC, autosomal or pseudoautosomal	Muir-Torre syndrome, MONDO:0008018						False	2	0;100;0	2.5	False		ENSG00000122512	ENSG00000122512	HGNC:9122