| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89284890C>T | CA10588635 | ANKRD11 | c.1652G>A (p.Trp551Ter) c.*1455G>A (n.*1455G>A) c.1277G>A (p.Trp426Ter) c.744+3638G>A (n.744+3638G>A) n.3424G>A n.1644G>A c.151+3638G>A c.1550G>A (p.Trp517Ter) c.1355G>A (p.Trp452Ter) c.1523G>A (p.Trp508Ter) | ClinVar dbSNP |
| 16 | g.89284890C= | CA2241602977 | ANKRD11 | c.1652G= (p.Trp551=) c.*1455G= (n.*1455G=) c.1277G= (p.Trp426=) c.744+3638G= (n.744+3638G=) n.3424G= n.1644G= c.151+3638G= c.1550G= (p.Trp517=) c.1355G= (p.Trp452=) c.1523G= (p.Trp508=) | dbSNP |