| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1026insG | p.Asp342GlufsX23 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAC | Asp | ins1c | Fs. | Stop at 364 |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status |
| 10_APC-119---1586P | Relative |
| Symptom |
| Reference ID | Reference |
| 10 | Unpublished data |