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
APC	gene	APC	Expert list;Expert Review;Expert Review Green	Thyroid Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Thyroid cancer, MONDO:0002108;Thyroid gland papillary carcinoma, MONDO:0005075;Familial adenomatous polyposis 1, MONDO:0021056;Adenomatous polyposis coli, MIM#175100			Neoplasm of the thyroid gland;HP:0100031			False	3	100;0;0	1.1	True		ENSG00000134982	ENSG00000134982	HGNC:583													
CDKN1B	gene	CDKN1B	Expert list;Expert Review;Expert Review Green	Thyroid Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Thyroid cancer, MONDO:0002108;Thyroid gland papillary carcinoma, MONDO:0005075;Multiple endocrine neoplasia type 4, MONDO:0012552;Multiple endocrine neoplasia, type 4, MIM#610755			Neoplasm of the thyroid gland;HP:0100031			False	3	100;0;0	1.1	True		ENSG00000111276	ENSG00000111276	HGNC:1785													
DICER1	gene	DICER1	Expert list;Expert Review;Expert Review Green	Thyroid Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Thyroid cancer, MONDO:0002108;Thyroid gland papillary carcinoma, MONDO:0005075;DICER1-related tumor predisposition, MONDO:0100216;DICER1 syndrome, MIM#601200			Neoplasm of the thyroid gland;HP:0100031			False	3	100;0;0	1.1	True		ENSG00000100697	ENSG00000100697	HGNC:17098													
PRKAR1A	gene	PRKAR1A	Expert list;Expert Review;Expert Review Green	Thyroid Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Thyroid cancer, MONDO:0002108;Thyroid gland follicular carcinoma, MONDO:0005034;Carney complex type 1, MONDO:0008057;Carney complex, type 1, MIM#160980			Neoplasm of the thyroid gland;HP:0100031			False	3	100;0;0	1.1	True		ENSG00000108946	ENSG00000108946	HGNC:9388													
PTEN	gene	PTEN	Expert list;Expert Review;Expert Review Green	Thyroid Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Thyroid cancer, MONDO:0002108;Thyroid gland follicular carcinoma, MONDO:0005034;PTEN hamartoma tumor syndrome, MONDO:0017623;PTEN hamartoma tumour syndromes, MIM#158350			Neoplasm of the thyroid gland;HP:0100031			False	3	100;0;0	1.1	True		ENSG00000171862	ENSG00000171862	HGNC:9588													
RET	gene	RET	Expert list;Expert Review;Expert Review Green	Thyroid Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Thyroid cancer, MONDO:0002108;Medullary thyroid gland carcinoma, MONDO:0015277;Multiple endocrine neoplasia type 2A, MONDO:0008234;Multiple endocrine neoplasia type 2B, MONDO:0008082;Multiple endocrine neoplasia, type 2A, MIM#171400;Multiple endocrine neoplasia, type 2B, MIM#162300;Pheochromocytoma, MIM#171300;Medullary thyroid carcinoma, MIM#155240;Pheochromocytoma, susceptibility to, MIM#171300			Neoplasm of the thyroid gland;HP:0100031			False	3	100;0;0	1.1	True	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