| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41571515G>C | CA115911 | KRT9 | c.478C>G (p.Leu160Val) c.-189-33C>G (n.-189-33C>G) | ClinVar dbSNP |
| 17 | g.41571515G>A | CA115914 | KRT9 | c.478C>T (p.Leu160Phe) c.-189-33C>T (n.-189-33C>T) | ClinVar dbSNP |
| 17 | g.41571515G= | CA2260079916 | KRT9 | c.478C= (p.Leu160=) c.-189-33C= (n.-189-33C=) | dbSNP |