| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.52515040G>A | CA6582420 | KRT5 | c.1675C>T (p.Arg559Ter) n.600C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 12 | g.52515040G>C | CA384974770 | KRT5 | c.1675C>G (p.Arg559Gly) n.600C>G | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.52515040G= | CA2036538126 | KRT5 | c.1675C= (p.Arg559=) n.600C= | dbSNP |