| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.52906134T>C | CA127073 | DCC | c.503T>C (p.Met168Thr) c.304T>C c.434T>C (p.Met145Thr) c.424T>C n.416T>C c.424T>C (n.424T>C) | ClinVar dbSNP |
| 18 | g.52906134T= | CA2303875036 | DCC | c.503T= (p.Met168=) c.304T= c.434T= (p.Met145=) c.424T= n.416T= c.424T= (n.424T=) | dbSNP |