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
230817102554_ebce	GeneID	148398	NGG	install
230817102546_1b4h	AlleleID	929884	NGG	install
230717154445_uxh2	GeneSymbol	SAMD11	NGG	install
230712161355_nhen	AlleleID	929884	NGG	install
230712161328_ic53	GeneSymbol	SAMD11	NGG	install
230711232017_1wyt	AlleleID	526296	NGG	install
230705085630_avbz	GeneSymbol	SAMD11	NGG	install
230704111347_85k0	HGNC_ID	28706	NGG	install
230704111342_xokw	GeneSymbol	SAMD11	NGG	install
230704111333_8bac	GeneID	148398	NGG	install