OPED
HOME
DESIGN
BY SEQUENCE
BY POSITION
OPEDVAR
HELP
CONTACT
Welcome to OPEDVar!
Use an example
AlleleID
GeneID
GeneSymbol
HGNC_ID
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