Welcome to OPEDVar!

Use an example AlleleID GeneID GeneSymbol HGNC_ID QUERY TYPE Select query type and 'AlleleID', 'GeneID', 'GeneSymbol' and 'HGNC_ID' QUERY ITEM Enter the AlleleID,GeneID,GeneSymbol or HGNC_ID PAM Select PAM type between 'NGG' and 'NG' DIRECTION Select edit direction which means to install or correct pathogenic human genetic variants ASSEMBLY

HISTORY

UID	Query Type	Query Item	PAM	Direction
240104210402_lz64	GeneSymbol	MTHFR	NGG	correct
240104145304_onrn	GeneSymbol	PJVK	NG	correct
240104145243_1hso	GeneSymbol	PJVK	NGG	install
240104144713_0v9e	GeneSymbol	PJVK	NGG	correct
240103132153_ex3l	AlleleID	929884	NGG	install
240103132058_zq1p	GeneSymbol	HBB	NGG	install
240103132006_4gxl	AlleleID	15447	NGG	install
240101180217_wzxw	GeneSymbol	KRAS	NGG	install
231224232218_xn48	GeneSymbol	ATP7B	NGG	correct
231221131442_k5er	GeneSymbol	KRAS	NGG	correct