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
230817214749_hnkc	AlleleID	929884	NGG	install
230817102645_dpmt	AlleleID	929884	NGG	install
230817102634_dyj5	GeneSymbol	SAMD11	NGG	install
230817102616_4ydz	AlleleID	929884	NGG	install
230817102605_k9ho	GeneID	148398	NGG	install
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