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
231104173834_z0zc	GeneID	3039	NGG	install
231104173834_gzl8	GeneID	3039	NGG	install
231104145644_4la1	AlleleID	929884	NGG	install
231103155457_599m	GeneID	148398	NGG	install
231102191534_f4q8	GeneSymbol	NF1	NGG	install
231102022245_iphz	GeneSymbol	HEXA	NGG	install
231102022234_rn43	GeneSymbol	HEXA	NGG	install
231102015809_d96m	GeneSymbol	HEXA	NGG	install
231102015324_mnrg	GeneSymbol	HEXA	NGG	install
231030125057_5ac7	GeneSymbol	SAMD11	NGG	install