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
BRAF	gene	BRAF	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Amber;Victorian Clinical Genetics Services	Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	RASopathies;Focal cortical dysplasia				18039946;18039235;25356392		False	2	0;100;0	0.48	True		ENSG00000157764	ENSG00000157764	HGNC:1097													
STRADA	gene	STRADA	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Amber;Victorian Clinical Genetics Services	Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Polyhydramnios, megalencephaly, and symptomatic epilepsy (MIM#611087)				28688840;17522105;27170158;23616120		False	2	100;0;0	0.48	True		ENSG00000266173	ENSG00000266173	HGNC:30172