| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89283458G>C | CA397160636 | ANKRD11 | c.3084C>G (p.Tyr1028Ter) c.*2887C>G (n.*2887C>G) c.2709C>G (p.Tyr903Ter) c.744+5070C>G (n.744+5070C>G) c.151+5070C>G c.2982C>G (p.Tyr994Ter) c.2787C>G (p.Tyr929Ter) c.2955C>G (p.Tyr985Ter) | ClinVar dbSNP |
| 16 | g.89283458G>T | CA16620308 | ANKRD11 | c.3084C>A (p.Tyr1028Ter) c.*2887C>A (n.*2887C>A) c.2709C>A (p.Tyr903Ter) c.744+5070C>A (n.744+5070C>A) c.151+5070C>A c.2982C>A (p.Tyr994Ter) c.2787C>A (p.Tyr929Ter) c.2955C>A (p.Tyr985Ter) | ClinVar dbSNP |