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
240103132058_zq1p	GeneSymbol	HBB	NGG	install
240103132006_4gxl	AlleleID	15447	NGG	install
240101180217_wzxw	GeneSymbol	KRAS	NGG	install
231224232218_xn48	GeneSymbol	ATP7B	NGG	correct
231221131442_k5er	GeneSymbol	KRAS	NGG	correct
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