| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89282980G>A | CA10603423 | ANKRD11 | c.3562C>T (p.Arg1188Ter) c.*3365C>T (n.*3365C>T) c.744+5548C>T (n.744+5548C>T) c.151+5548C>T c.3460C>T (p.Arg1154Ter) c.3265C>T (p.Arg1089Ter) c.3433C>T (p.Arg1145Ter) | ClinVar dbSNP gnomAD v2 COSMIC |
| 16 | g.89282980G>T | CA497374723 | ANKRD11 | c.3562C>A (p.Arg1188=) c.*3365C>A (n.*3365C>A) c.744+5548C>A (n.744+5548C>A) c.151+5548C>A c.3460C>A (p.Arg1154=) c.3265C>A (p.Arg1089=) c.3433C>A (p.Arg1145=) | dbSNP |