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
230819115007_nhna	AlleleID	929884	NGG	install
230819114727_8s3q	AlleleID	929884	NGG	install
230819114715_4fb1	GeneSymbol	SAMD11	NGG	install
230819114030_z7x5	GeneSymbol	SAMD11	NGG	install
230819114021_bmli	GeneID	148398	NGG	install
230819114013_0xnd	AlleleID	929884	NGG	install
230819114005_2mfc	GeneID	148398	NGG	install
230819113405_bmn5	GeneID	148398	NGG	install
230819095825_0w9z	GeneID	11315	NGG	install
230819095623_q2vs	GeneSymbol	SAMD11	NGG	install