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
260428142100_1flg	GeneSymbol	SAMD11	NGG	install
260428142054_o3lf	GeneID	148398	NGG	correct
260417093259_9cyg	GeneSymbol	PIK3CA	NGG	install
260417093237_0qfp	GeneID	5290	NGG	install
260417093101_cbzt	GeneSymbol	NFE2L2	NGG	install
260415180441_1ol1	AlleleID	1065550	NGG	install
260415180415_dnm6	GeneSymbol	EXOSC1	NGG	install
260415174813_bghv	GeneSymbol	EXOSC1	NGG	install
260402170918_6nm6	GeneSymbol	LMNA	NG	correct
260402170816_yif6	GeneSymbol	LMNA	NG	correct