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 20220616170710
AlleleID 929884 NGG install 20220523202906
GeneID 4297 NGG install 20220514151628
GeneID 4297 NGG install 20220514120308
AlleleID 929884 NGG install 20220514120044
AlleleID 929884 NGG install 20220514000100
AlleleID 929884 NGG install 20220513215413
AlleleID 929884 NGG install 20220513215205
AlleleID 929884 NGG correct 20220513214039
AlleleID 929884 NGG install 20220513213602