| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.112780895C>G | CA16022734 | APC | c.637C>G (p.Arg213Gly) n.693C>G c.*643C>G (n.*643C>G) c.667C>G (p.Arg223Gly) c.562C>G (p.Arg188Gly) c.460C>G (p.Arg154Gly) c.-399C>G (n.-399C>G) | ClinVar dbSNP |
| 5 | g.112780895C>T | CA011131 | APC | c.637C>T (p.Arg213Ter) n.693C>T c.*643C>T (n.*643C>T) c.667C>T (p.Arg223Ter) c.562C>T (p.Arg188Ter) c.460C>T (p.Arg154Ter) c.-399C>T (n.-399C>T) | ClinVar dbSNP COSMIC |
| 5 | g.112780895C>A | CA445755526 | APC | c.637C>A (p.Arg213=) n.693C>A c.*643C>A (n.*643C>A) c.667C>A (p.Arg223=) c.562C>A (p.Arg188=) c.460C>A (p.Arg154=) c.-399C>A (n.-399C>A) | ClinVar dbSNP |