Welcome to OPEDVar!


Use an example AlleleID GeneID GeneSymbol HGNC_ID 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
UID Query Type Query Item PAM Direction
230630153934_3wk6 GeneSymbol SAMD11 NGG install
230630152454_8755 AlleleID 929884 NGG install
230630152452_yjsb HGNC_ID 28706 NGG install
230630152449_vs89 GeneSymbol SAMD11 NGG install
230630152443_je3n GeneSymbol SAMD11 NGG install