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
241124210445_jivn	GeneSymbol	FLT3	NGG	install
241124205600_i522	GeneID	2322	NGG	install
241121172641_4hsn	GeneSymbol	FLG	NGG	install
241105222737_gqt2	GeneID	7399	NGG	correct
241022152549_a6m4	GeneSymbol	SAMD11	NGG	install
241022152540_te18	GeneID	148398	NGG	install
241022152447_t4lz	GeneSymbol	SAMD11	NGG	install
241017172915_73tr	GeneSymbol	GJB2	NGG	correct
240912030715_2yvk	GeneID	148398	NGG	install
240829121522_ia7j	GeneSymbol	ERCC4	NGG	install