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
231221002953_k985	GeneSymbol	SF3B1	NG	install
231219025710_ng04	GeneSymbol	CLCC1	NGG	install
231218170239_s90p	AlleleID	30486	NGG	install
231218170057_4e7i	AlleleID	30486	NGG	correct
231218165950_g1yn	GeneSymbol	HBB	NGG	correct
231218165911_qdw8	AlleleID	15447	NGG	correct
231215130350_uhmp	GeneSymbol	SNCA	NGG	install
231215130335_oamm	GeneSymbol	SNCA	NGG	install
231215125813_kegp	GeneSymbol	SNCA	NGG	install
231213053157_li90	AlleleID	414728	NGG	install