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
231213052639_pq1f	AlleleID	48221	NGG	install
231213052606_5ylj	AlleleID	48259	NGG	install
231213052500_rsy2	AlleleID	48221	NGG	install
231213052424_hn9u	AlleleID	414728	NGG	install
231213051621_mzww	GeneSymbol	DYRK1A	NGG	install
231213051457_ggd4	GeneSymbol	CACNA1A	NGG	install
231210021709_ustj	GeneSymbol	CFTR	NGG	correct
231207145920_gh85	GeneID	148398	NGG	install
231205210455_pld5	GeneSymbol	GPX4	NGG	install
231205055238_0szi	AlleleID	929884	NGG	install