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
A2ML1	gene	A2ML1	Expert Review Red;Victorian Clinical Genetics Services	Rasopathy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Noonan syndrome			Rasopathy;MONDO:0021060	24939586;25862627		False	1	0;0;100	0.113	True		ENSG00000166535	ENSG00000166535	HGNC:23336													
KAT6B	gene	KAT6B	ClinGen;Expert Review Red	Rasopathy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	RASopathy, MONDO:0021060			Rasopathy;MONDO:0021060			False	1	0;0;100	0.113	True		ENSG00000156650	ENSG00000156650	HGNC:17582													
NSUN2	gene	NSUN2	ClinGen;Expert Review Red	Rasopathy		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	RASopathy, MONDO:0021060			Rasopathy;MONDO:0021060			False	1	0;0;100	0.113	True		ENSG00000037474	ENSG00000037474	HGNC:25994													
RASA1	gene	RASA1	ClinGen;Expert Review Red	Rasopathy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Noonan syndrome, MONDO:0018997			Rasopathy;MONDO:0021060			False	1	0;0;100	0.113	True		ENSG00000145715	ENSG00000145715	HGNC:9871