| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.3185_3188delAAAG | p.Gln1062LeufsX63 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAA | Gln | del4b | Fs. | Stop at 1124 | Fr. |
| 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_-4101G06036G06036 | Relative |
| Symptom |
| Reference ID | Reference |
| 71 | Unpublished data |