| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41583772C>T | CA216990 | KRT14 | c.915G>A (p.Trp305Ter) n.365G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41583772C= | CA2260085563 | KRT14 | c.915G= (p.Trp305=) n.365G= | dbSNP |
| 17 | g.41583772C>G | CA399477074 | KRT14 | c.915G>C (p.Trp305Cys) n.365G>C | dbSNP |