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
240605131821_awov	GeneSymbol	CFTR	NGG	correct
240601235656_ajkt	GeneSymbol	SAMD11	NGG	install
240530234603_3nq9	AlleleID	264183	NGG	correct
240530234547_f5sl	AlleleID	264183	NGG	install
240530234531_x0vo	AlleleID	264183	NGG	correct
240530233909_nn9h	AlleleID	264183	NGG	correct
240530232138_et7d	AlleleID	264183	NGG	correct
240530230448_mtxs	AlleleID	929884	NGG	install
240530223248_foxy	GeneID	1294	NGG	correct
240530222814_5fw3	AlleleID	929884	NGG	install