"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CTSF"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259167	NM_003793.4(CTSF):c.1368C>T (p.Asp456=)	CTSF	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 1216529	NM_003793.4(CTSF):c.1322-19G>A	CTSF	Single nucleotide variant (intron variant)	Neuronal ceroid lipofuscinosis 13 +1 more	GBenign/Likely benign
Select item 259173	NM_003793.4(CTSF):c.939G>A (p.Gly313=)	CTSF	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +3 more	GBenign/Likely benign

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