| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.112775683C>G | CA10584237 | APC | c.477C>G (p.Tyr159Ter) n.533C>G c.*483C>G (n.*483C>G) c.507C>G (p.Tyr169Ter) c.402C>G (p.Tyr134Ter) c.300C>G (p.Tyr100Ter) c.-559C>G (n.-559C>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.112775683C>T | CA337609 | APC | c.477C>T (p.Tyr159=) n.533C>T c.*483C>T (n.*483C>T) c.507C>T (p.Tyr169=) c.402C>T (p.Tyr134=) c.300C>T (p.Tyr100=) c.-559C>T (n.-559C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.112775683C>A | CA16022367 | APC | c.477C>A (p.Tyr159Ter) n.533C>A c.*483C>A (n.*483C>A) c.507C>A (p.Tyr169Ter) c.402C>A (p.Tyr134Ter) c.300C>A (p.Tyr100Ter) c.-559C>A (n.-559C>A) | ClinVar dbSNP |