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
250403213616_5fbx	HGNC_ID	6893	NGG	correct
250403213548_kjeb	HGNC_ID	6893	NGG	install
250402105338_aje0	GeneID	3043	NGG	correct
250402101337_a6gc	GeneID	3043	NGG	correct
250306184112_uag4	GeneSymbol	BAG3	NGG	correct
250306183935_3rpq	GeneSymbol	BAG3	NGG	install
250212090010_snfb	HGNC_ID	4284	NGG	install
250210192535_cs42	GeneSymbol	FLT3	NGG	install
250210192227_4yvp	GeneSymbol	FLT3	NGG	install
250210151123_r4zl	AlleleID	929884	NGG	install