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 Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Tumor predisposition syndrome, MIM# 614327				21941004;23684012;21874000;21874003		False	1	0;0;100	0.131	True		ENSG00000163930	ENSG00000163930	HGNC:950													
CDC73	gene	CDC73	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parathyroid carcinoma, MIM# 608266						False	1	0;0;100	0.131	True		ENSG00000134371	ENSG00000134371	HGNC:16783													
CDK4	gene	CDK4	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Melanoma, cutaneous malignant, 3}, MIM# 609048						False	1	0;0;100	0.131	True		ENSG00000135446	ENSG00000135446	HGNC:1773													
CDKN2A	gene	CDKN2A	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Familial Malignant Melanoma and Tumors of the Nervous system;Familial Uveal Melanoma;Pancreatic cancer						False	1	0;0;100	0.131	True		ENSG00000147889	ENSG00000147889	HGNC:1787													
EPCAM	gene	EPCAM	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Colorectal cancer, hereditary nonpolyposis, type 8, MIM# 613244						False	1	0;0;100	0.131	True		ENSG00000119888	ENSG00000119888	HGNC:11529													
FANCM	gene	FANCM	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	BIALLELIC, autosomal or pseudoautosomal	Fanconi anaemia				28837162		False	1	0;0;100	0.131	True		ENSG00000187790	ENSG00000187790	HGNC:23168													
MUTYH	gene	MUTYH	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	BIALLELIC, autosomal or pseudoautosomal	Adenomas, multiple colorectal, MIM# 608456						False	1	0;0;100	0.131	True		ENSG00000132781	ENSG00000132781	HGNC:7527													
NOP10	gene	NOP10	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	BIALLELIC, autosomal or pseudoautosomal	Dyskeratosis congenita, autosomal recessive 1, MIM#224230				17507419		False	1	0;0;100	0.131	True		ENSG00000182117	ENSG00000182117	HGNC:14378													
RAD51C	gene	RAD51C	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group O, MIM# 613390				20400963;29278735		False	1	0;0;100	0.131	True		ENSG00000108384	ENSG00000108384	HGNC:9820													
TMEM127	gene	TMEM127	Expert Review Red;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Pheochromocytoma, susceptibility to}, MIM# 171300						False	1	0;0;100	0.131	True		ENSG00000135956	ENSG00000135956	HGNC:26038