| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.2314dup | p.Thr772AsnfsX3 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| ACT | Thr | ins1b | Fs. | Stop at 774 |
| 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 |
| SO_-1706G00033G00033 | Relative |
| Symptom |
| Reference ID | Reference |
| 71 | Unpublished data |