| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41586479A>G | CA216901 | KRT14 | c.356T>C (p.Met119Thr) | ClinVar dbSNP |
| 17 | g.41586479A>C | CA399482585 | KRT14 | c.356T>G (p.Met119Arg) | ClinVar dbSNP |
| 17 | g.41586479A= | CA2260086841 | KRT14 | c.356T= (p.Met119=) | dbSNP |