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
240321151915_qvg7	GeneID	148398	NGG	install
240321151735_avr2	GeneID	148398	NGG	install
240321151628_o7tn	GeneID	148398	NGG	install
240319213247_42vr	GeneSymbol	SAMD11	NGG	install
240314223044_lhyv	AlleleID	929884	NGG	install
240314223029_02d1	GeneSymbol	SAMD11	NGG	install
240314222652_z6uy	GeneSymbol	GALNS	NGG	install
240314222539_grb6	AlleleID	929884	NGG	install
240227234803_ozu8	AlleleID	929884	NGG	install
240222010704_nay5	GeneSymbol	GALNS	NGG	correct