| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.112767234C>G | CA10578287 | APC | c.266C>G (p.Ser89Ter) n.322C>G c.*272C>G (n.*272C>G) c.296C>G (p.Ser99Ter) c.191C>G (p.Ser64Ter) c.89C>G (p.Ser30Ter) c.-770C>G (n.-770C>G) | ClinVar dbSNP |
| 5 | g.112767234C>T | CA16021921 | APC | c.266C>T (p.Ser89Leu) n.322C>T c.*272C>T (n.*272C>T) c.296C>T (p.Ser99Leu) c.191C>T (p.Ser64Leu) c.89C>T (p.Ser30Leu) c.-770C>T (n.-770C>T) | ClinVar dbSNP COSMIC |
| 5 | g.112767234C>A | CA16021920 | APC | c.266C>A (p.Ser89Ter) n.322C>A c.*272C>A (n.*272C>A) c.296C>A (p.Ser99Ter) c.191C>A (p.Ser64Ter) c.89C>A (p.Ser30Ter) c.-770C>A (n.-770C>A) | ClinVar dbSNP |