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
GeneID 4088 NGG install 20220928222800
AlleleID 526296 NGG install 20220921224708
AlleleID 929884 NGG install 20220918224726
AlleleID 929884 NGG install 20220902094801
AlleleID 929884 NGG install 20220901093111
AlleleID 929884 NGG install 20220901093107
AlleleID 929884 NGG install 20220831130623
AlleleID 929884 NGG install 20220616170710
AlleleID 929884 NGG install 20220523202906
GeneID 4297 NGG install 20220514151628