Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.133352518A>G | CA128719 | SURF1 | c.679T>C (p.Trp227Arg) n.589T>C n.669T>C c.352T>C (p.Trp118Arg) | ClinVar dbSNP |
9 | g.133352518A>T | CA375693747 | SURF1 | c.679T>A (p.Trp227Arg) n.589T>A n.669T>A c.352T>A (p.Trp118Arg) | ClinVar dbSNP |
9 | g.133352518A= | CA1882634161 | SURF1 | c.679T= (p.Trp227=) n.589T= n.669T= c.352T= (p.Trp118=) | dbSNP |