| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41624214A>G | CA216623 | KRT17 | c.296T>C (p.Leu99Pro) c.-312-8T>C (n.-312-8T>C) n.362T>C n.83T>C c.71+20T>C (n.71+20T>C) c.251T>C (p.Leu84Pro) | ClinVar dbSNP |
| 17 | g.41624214A= | CA2260105455 | KRT17 | c.296T= (p.Leu99=) c.-312-8T= (n.-312-8T=) n.362T= n.83T= c.71+20T= (n.71+20T=) c.251T= (p.Leu84=) | dbSNP |