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
230819164217_dh3c	GeneID	375790	NGG	correct
230819163803_vi40	GeneSymbol	AGRN	NGG	correct
230819163604_sa5v	GeneSymbol	ISG15	NGG	correct
230819163353_ebhu	AlleleID	1015460	NGG	correct
230819163105_4btw	AlleleID	929884	NG	correct
230819163019_lmfs	AlleleID	929884	NGG	correct
230819162839_xub6	AlleleID	929884	NG	install
230819162523_jp1p	AlleleID	929884	NGG	correct
230819162150_q73y	AlleleID	929884	NGG	install
230819161833_b0xt	GeneID	148398	NGG	install