| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.26026470G>T | CA354977 | MYO18B | c.6496G>T (p.Glu2166Ter) c.6499G>T (p.Glu2167Ter) n.5067G>T c.*3954G>T (n.*3954G>T) c.345G>T c.6625G>T (p.Glu2209Ter) c.6622G>T (p.Glu2208Ter) c.6142G>T (p.Glu2048Ter) c.6493G>T (p.Glu2165Ter) c.3961G>T (p.Glu1321Ter) c.3958G>T (p.Glu1320Ter) | ClinVar dbSNP |
| 22 | g.26026470G= | CA2399004076 | MYO18B | c.6496G= (p.Glu2166=) c.6499G= (p.Glu2167=) n.5067G= c.*3954G= (n.*3954G=) c.345G= c.6625G= (p.Glu2209=) c.6622G= (p.Glu2208=) c.6142G= (p.Glu2048=) c.6493G= (p.Glu2165=) c.3961G= (p.Glu1321=) c.3958G= (p.Glu1320=) | dbSNP |