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
EXT1	gene	EXT1	Expert Review Green;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Chondrosarcoma, OMIM:215300;Chondrosarcoma (disease), MONDO:0008977				23770606;29529714;10441575		False	3	100;0;0	1.82	False		ENSG00000182197	ENSG00000182197	HGNC:3512													
EXT2	gene	EXT2	Expert Review Green;NHS GMS;Other	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Exostoses, multiple, type 2, OMIM:133701;Exostoses, multiple, type 2, MONDO:0007586				27636706;7726168;29529714;23770606		False	3	100;0;0	1.82	False		ENSG00000151348	ENSG00000151348	HGNC:3513													
MTAP	gene	MTAP	Expert list;Expert Review Green;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Diaphyseal medullary stenosis with malignant fibrous histiocytoma, OMIM:112250;Diaphyseal medullary stenosis-bone malignancy syndrome, MONDO:0007205				19197386;22464254		False	3	100;0;0	1.82	False		ENSG00000099810	ENSG00000099810	HGNC:7413													
NF1	gene	NF1	Expert Review Green;Expert Review Red;Literature;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Neurofibromatosis, type 1, OMIM:162200;Neurofibromatosis type 1, MONDO:0018975						False	3	100;0;0	1.82	False		ENSG00000196712	ENSG00000196712	HGNC:7765													
RECQL4	gene	RECQL4	Expert list;Expert Review Green;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	BIALLELIC, autosomal or pseudoautosomal	RAPADILINO syndrome, OMIM:266280;Rothmund-Thomson syndrome, type 2, OMIM:268400;Osteosarcoma (disease), MONDO:0009807				12734318;17264332;12612652;28338660		False	3	100;0;0	1.82	False		ENSG00000160957	ENSG00000160957	HGNC:9949													
SQSTM1	gene	SQSTM1	Expert list;Expert Review Green;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Paget disease of bone 3, OMIM:167250;Paget disease of bone 3, MONDO:0008176;Osteosarcoma (disease), MONDO:0009807				21437228;11473345;9345096;12374763		False	3	100;0;0	1.82	False		ENSG00000161011	ENSG00000161011	HGNC:11280													
T	gene	T	Expert list;Expert Review Green;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Chordoma (disease), MONDO:0008978				23064415;19801981;34837714		False	3	100;0;0	1.82	False		ENSG00000164458	ENSG00000164458	HGNC:11515													
TP53	gene	TP53	Expert Review Green;NHS GMS	Sarcoma susceptibility		Cancer susceptibility	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Li-Fraumeni syndrome, OMIM:151623;Solitary Fibrous Tumour;Sarcoma, MONDO:0005089				27050224;28338660;31529158		False	3	100;0;0	1.82	False		ENSG00000141510	ENSG00000141510	HGNC:11998