| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41612327A>C | CA16620406 | KRT16 | c.362T>G (p.Met121Arg) n.439T>G c.-312-41T>G (n.-312-41T>G) | ClinVar dbSNP |
| 17 | g.41612327A>T | CA217375 | KRT16 | c.362T>A (p.Met121Lys) n.439T>A c.-312-41T>A (n.-312-41T>A) | ClinVar dbSNP |
| 17 | g.41612327A>G | CA217377 | KRT16 | c.362T>C (p.Met121Thr) n.439T>C c.-312-41T>C (n.-312-41T>C) | ClinVar dbSNP |