| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.52676314A>G | CA126046 | KRT1 | c.1436T>C (p.Ile479Thr) n.510T>C | ClinVar dbSNP |
| 12 | g.52676314A>T | CA384962305 | KRT1 | c.1436T>A (p.Ile479Asn) n.510T>A | dbSNP |
| 12 | g.52676314A= | CA2036619572 | KRT1 | c.1436T= (p.Ile479=) n.510T= | dbSNP |