| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.110236135del | CA273599 | RDX | c.1308del (p.Lys438ArgfsTer26) n.537del c.267del (p.Lys91ArgfsTer26) n.318del c.*778del (n.*778del) c.405-4131del (n.405-4131del) n.423del c.900del (p.Lys302ArgfsTer26) | ClinVar dbSNP |
| 11 | g.110236135C= | CA3182810888 | RDX | c.1308G= (p.Lys436=) n.537G= c.267G= (p.Lys89=) n.318G= c.*778G= (n.*778G=) c.405-4131G= (n.405-4131G=) n.423G= c.900G= (p.Lys300=) | dbSNP |