OPED
HOME
OPED
SEQUENCE
POSITION
OPEDVar
OPEDVar
OPEDVar
QUERY TYPE
AlleleID
GeneID
GeneSymbol
HGNC_ID
Select query type and 'AlleleID','GeneID',
'GeneSymbol' and 'HGNC_ID'
QUERY ITEM
Enter the AlleleID,GeneID,GeneSymbol or HGNC_ID
PAM
NGG
NG
Select PAM type between 'NGG' and 'NG'
DIRECTION
install
correct
Select edit direction which means to install
or correct pathogenic human genetic variants
ASSEMBLY
GRch38
HISTORY