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
251229212515_52yl	AlleleID	29732	NGG	correct
251229210940_9hsv	GeneSymbol	SLC26A4	NGG	correct
251112022429_w6ke	GeneSymbol	SAMD11	NGG	install
251112022205_d5xp	AlleleID	929884	NGG	install
251107014622_pt7b	GeneSymbol	TP53	NGG	install
250806105403_dk0s	GeneID	7157	NGG	install
250730224234_cebw	GeneSymbol	ATR	NGG	install
250711095234_7jmn	GeneSymbol	LMNA	NGG	install
250519013652_8tuv	GeneID	148398	NGG	install
250519013005_ct5w	GeneID	148398	NGG	install