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
231108170723_dxa4	GeneSymbol	SAMD11	NGG	install
231107233825_qo5e	GeneSymbol	CLCC1	NGG	install
231107111000_3124	GeneSymbol	GJB2	NGG	correct
231105214635_m0ix	GeneID	148398	NGG	install
231105150002_eg8h	GeneID	5172	NGG	correct
231105145953_fe8e	GeneID	5172	NGG	install
231105135215_c3kz	GeneID	351	NGG	correct
231105132133_nhjy	GeneID	2706	NGG	correct
231105131727_ttdd	AlleleID	929884	NGG	install
231104173925_xyrj	GeneID	3039	NGG	install