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
CD247	gene	CD247	Emory Genetics Laboratory;Expert Review Red	SCID	Primary immunodeficiency disorders	Haematological disorders	BIALLELIC, autosomal or pseudoautosomal	T-B+ SCID				16672702		False	1	0;0;100	1.9	True		ENSG00000198821	ENSG00000198821	HGNC:1677													
ORAI1	gene	ORAI1	Emory Genetics Laboratory;Expert Review Red	SCID	Primary immunodeficiency disorders	Haematological disorders		T-B+ SCID;immunodeficiency, ectodermal dysplasia and myopathy				16582901;20004786		False	1	0;33;67	1.9	True		ENSG00000182500	ENSG00000276045	HGNC:25896													
RAC2	gene	RAC2	Emory Genetics Laboratory;Expert Review Red	SCID	Primary immunodeficiency disorders	Haematological disorders		T-B- SCID; T-B+ SCID						False	1	0;0;100	1.9	True		ENSG00000128340	ENSG00000128340	HGNC:9802													
STAT5B	gene	STAT5B	Emory Genetics Laboratory;Expert Review Red	SCID	Primary immunodeficiency disorders	Haematological disorders		T-B+ SCID						False	1	0;0;100	1.9	True		ENSG00000173757	ENSG00000173757	HGNC:11367													
STIM1	gene	STIM1	Emory Genetics Laboratory;Expert Review Red	SCID	Primary immunodeficiency disorders	Haematological disorders		T-B+ SCID						False	1	0;0;100	1.9	True		ENSG00000167323	ENSG00000167323	HGNC:11386