| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41583872A>G | CA216980 | KRT14 | c.815T>C (p.Met272Thr) n.265T>C | ClinVar dbSNP |
| 17 | g.41583872A>C | CA216982 | KRT14 | c.815T>G (p.Met272Arg) n.265T>G | ClinVar dbSNP |
| 17 | g.41583872A>T | CA399477592 | KRT14 | c.815T>A (p.Met272Lys) n.265T>A | ClinVar dbSNP |
| 17 | g.41583872A= | CA2260085601 | KRT14 | c.815T= (p.Met272=) n.265T= | dbSNP |