| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41624218A>C | CA216620 | KRT17 | c.292T>G (p.Tyr98Asp) c.-312-12T>G (n.-312-12T>G) n.358T>G n.79T>G c.71+16T>G (n.71+16T>G) c.247T>G (p.Tyr83Asp) | ClinVar dbSNP |
| 17 | g.41624218A= | CA2260105459 | KRT17 | c.292T= (p.Tyr98=) c.-312-12T= (n.-312-12T=) n.358T= n.79T= c.71+16T= (n.71+16T=) c.247T= (p.Tyr83=) | dbSNP |