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
230630153941_8fgk	GeneSymbol	SAMD11	NGG	install
230630153940_x964	GeneSymbol	SAMD11	NGG	install
230630153940_njlx	GeneSymbol	SAMD11	NGG	install
230630153940_n7l5	GeneSymbol	SAMD11	NGG	install
230630153940_jpj6	GeneSymbol	SAMD11	NGG	install
230630153940_7pjt	GeneSymbol	SAMD11	NGG	install
230630153939_pzpc	GeneSymbol	SAMD11	NGG	install
230630153939_grma	GeneSymbol	SAMD11	NGG	install
230630153939_ctqm	GeneSymbol	SAMD11	NGG	install
230630153939_1c14	GeneSymbol	SAMD11	NGG	install