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
260902101113_5xub	GeneSymbol	HGD	NGG	correct
260902055745_fvwp	GeneSymbol	HGD	NG	correct
260902055723_6epz	GeneSymbol	HGD	NGG	correct
260602220919_was2	GeneSymbol	KRAS	NG	install
260602215639_i0ng	GeneSymbol	KRAS	NGG	install
260519194214_pbad	AlleleID	414286	NGG	install
260510174149_18l5	GeneSymbol	ATM	NGG	correct
260510173912_8fx3	HGNC_ID	795	NGG	correct
260510173652_udpx	HGNC_ID	795	NGG	correct
260510164400_ce9u	HGNC_ID	795	NGG	correct