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
SDHAF2	gene	SDHAF2	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex II deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	50;25;25	2.11	True		ENSG00000167985	ENSG00000167985	HGNC:26034													
SDHC	gene	SDHC	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex II deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	67;33;0	2.11	True		ENSG00000143252	ENSG00000143252	HGNC:10682