| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44704140G>A | CA10581231 | CEACAM16,CEACAM16-AS1 | c.505G>A (p.Gly169Arg) n.436-4963C>T n.373-4963C>T | ClinVar dbSNP |
| 19 | g.44704140G= | CA2338067602 | CEACAM16,CEACAM16-AS1 | c.505G= (p.Gly169=) n.436-4963C= n.373-4963C= | dbSNP |