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
231113192624_dtsy	AlleleID	929884	NGG	install
231113185844_5mz9	GeneSymbol	OPTN	NGG	install
231113185553_1m99	GeneSymbol	SAMD11	NGG	install
231111110536_pcpj	GeneID	148398	NGG	install
231110141832_929j	AlleleID	39328	NG	correct
231110141502_8ch9	AlleleID	39328	NGG	correct
231110141128_6wte	AlleleID	39328	NG	correct
231109142033_rv55	GeneSymbol	SAMD11	NGG	install
231108170723_dxa4	GeneSymbol	SAMD11	NGG	install
231107233825_qo5e	GeneSymbol	CLCC1	NGG	install