| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1621insAA | p.Gln541AsnfsX9 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAG | Gln | ins2a | Fs. | Stop at 549 |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| ASEF binding domain ARM2 |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status |
| SO_-1803G00498G00498 | Relative |
| Symptom |
| Reference ID | Reference |
| 71 | Unpublished data |