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
PDGFRA	gene	PDGFRA	Literature	Adult solid tumours for rare disease	Tumour syndromes	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial, OMIM:175510						False	1	0;100;0	1.42	False		ENSG00000134853	ENSG00000134853	HGNC:8803