| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.40866801A>G | CA119163 | KRT12 | c.386T>C (p.Met129Thr) c.278T>C (p.Met93Thr) n.1500+15941A>G n.2008+15941A>G | ClinVar dbSNP |
| 17 | g.40866801A= | CA2259745831 | KRT12 | c.386T= (p.Met129=) c.278T= (p.Met93=) n.1500+15941A= n.2008+15941A= | dbSNP |