| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41586438C>G | CA216939 | KRT14 | c.397G>C (p.Val133Leu) | ClinVar dbSNP |
| 17 | g.41586438C>T | CA216937 | KRT14 | c.397G>A (p.Val133Met) | ClinVar dbSNP COSMIC |
| 17 | g.41586438C>A | CA216941 | KRT14 | c.397G>T (p.Val133Leu) | ClinVar dbSNP |
| 17 | g.41586438C= | CA2260086817 | KRT14 | c.397G= (p.Val133=) | dbSNP |