OPEDVar

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

Query Type Query Item PAM Direction Time
AlleleID 929884 NGG install 20220513213307
GeneID 4297 NGG install 20220513210406
AlleleID 929884 NGG install 20220513210131
AlleleID 929884 NGG install 20220513204709