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
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
250210143823_e1wa	GeneSymbol	LMX1A	NGG	install
250206213701_dnn1	GeneSymbol	KRAS	NGG	install
250206213151_btl0	HGNC_ID	6407	NGG	install
250206212928_pj5t	HGNC_ID	28706	NGG	install
250206212741_ap5e	GeneSymbol	NRAS	NGG	install