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
CDKN1B	gene	CDKN1B	Expert list;Expert Review Green	Thyroid cancer pertinent cancer susceptibility	Pertinent cancer susceptibility gene panel	Cancer Programme	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Multiple endocrine neoplasia, type IV, OMIM:610755;Thyroid cancer;Pituitary adenoma				17030811		False	3	0;0;0	1.4	False		ENSG00000111276	ENSG00000111276	HGNC:1785													
PRKAR1A	gene	PRKAR1A	Expert list;Expert Review Green	Thyroid cancer pertinent cancer susceptibility	Pertinent cancer susceptibility gene panel	Cancer Programme	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Carney complex;Myxoma (cardiac or cutaneous or breast)				10973256;20301463		False	3	0;0;0	1.4	False		ENSG00000108946	ENSG00000108946	HGNC:9388													
PTEN	gene	PTEN	Expert list;Expert Review Green	Thyroid cancer pertinent cancer susceptibility	Pertinent cancer susceptibility gene panel	Cancer Programme	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Cowden Syndrome;PTEN hamartoma tumor syndrome;Breast cancer;Thyroid cancer;Endometrial cancer				9140396;20301661		False	3	0;0;0	1.4	False		ENSG00000171862	ENSG00000171862	HGNC:9588													
RET	gene	RET	Expert list;Expert Review Green	Thyroid cancer pertinent cancer susceptibility	Pertinent cancer susceptibility gene panel	Cancer Programme	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Multiple endocrine neoplasia 2A and 2B;Medullary thyroid cancer;Pheochromocytoma				8099202;20301434		False	3	0;0;0	1.4	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000165731	ENSG00000165731	HGNC:9967													
WRN	gene	WRN	Expert list;Expert Review Green	Thyroid cancer pertinent cancer susceptibility	Pertinent cancer susceptibility gene panel	Cancer Programme	BIALLELIC, autosomal or pseudoautosomal	Werner syndrome;Sarcoma;Melanoma;Thyroid cancer				8602509;20301687		False	3	0;0;0	1.4	False		ENSG00000165392	ENSG00000165392	HGNC:12791