| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41624247A>G | CA216606 | KRT17 | c.263T>C (p.Met88Thr) c.-312-41T>C (n.-312-41T>C) n.329T>C n.50T>C c.58T>C (p.Cys20Arg) c.218T>C (p.Met73Thr) | ClinVar dbSNP |
| 17 | g.41624247A>T | CA216605 | KRT17 | c.263T>A (p.Met88Lys) c.-312-41T>A (n.-312-41T>A) n.329T>A n.50T>A c.58T>A (p.Cys20Ser) c.218T>A (p.Met73Lys) | ClinVar dbSNP |