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
CDKN2A	gene	CDKN2A	Expert Review;Expert Review Green;Literature;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Melanoma, cutaneous malignant, 2}, OMIM:155601;{Melanoma and neural system tumor syndrome}, OMIM:155755;{Melanoma-pancreatic cancer syndrome}, OMIM:606719;melanoma, cutaneous malignant, susceptibility to, 2, MONDO:0007964;melanoma and neural system tumor syndrome, MONDO:0007967;melanoma-pancreatic cancer syndrome, MONDO:0011713				24884915;8317504;9622062;10797439;17440112;26794401;29263814;28699883;28754699;35422439;38936911		False	3	100;0;0	2.14	False		ENSG00000147889	ENSG00000147889	HGNC:1787													
DGCR8	gene	DGCR8	Expert Review Green;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown							False	3	100;0;0	2.14	False		ENSG00000128191	ENSG00000128191	HGNC:2847													
LZTR1	gene	LZTR1	Expert Review Green;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Schwannomatosis-2, susceptibility to}, OMIM:615670;LZTR1-related schwannomatosis, MONDO:0014299						False	3	100;0;0	2.14	False		ENSG00000099949	ENSG00000099949	HGNC:6742													
NF2	gene	NF2	Expert Review Green;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Schwannomatosis, vestibular, OMIM:101000;NF2-related schwannomatosis, MONDO:0007039						False	3	100;0;0	2.14	False		ENSG00000186575	ENSG00000186575	HGNC:7773													
SMARCB1	gene	SMARCB1	Expert Review Green;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Schwannomatosis-1, susceptibility to}, OMIM:162091;{Rhabdoid tumor predisposition syndrome 1}, OMIM:609322;rhabdoid tumor predisposition syndrome 1, MONDO:0012252;SMARCB1-related schwannomatosis, MONDO:0024517						False	3	100;0;0	2.14	False		ENSG00000099956	ENSG00000099956	HGNC:11103													
SMARCE1	gene	SMARCE1	Expert Review Green;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Meningioma, familial, susceptibility to}, OMIM:607174						False	3	100;0;0	2.14	False		ENSG00000073584	ENSG00000073584	HGNC:11109													
SUFU	gene	SUFU	Expert Review Green;NHS GMS	Familial tumours of the nervous system		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Medulloblastoma}, OMIM:155255;{Meningioma, familial, susceptibility to}, OMIM:607174						False	3	100;0;0	2.14	False		ENSG00000107882	ENSG00000107882	HGNC:16466