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
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
260510162223_gvzd	GeneSymbol	ATM	NGG	correct
260510162134_m996	GeneSymbol	ATM	NGG	correct
260510161949_nnh8	GeneSymbol	ATM	NGG	correct
260428142100_1flg	GeneSymbol	SAMD11	NGG	install
260428142054_o3lf	GeneID	148398	NGG	correct
260417093259_9cyg	GeneSymbol	PIK3CA	NGG	install