| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.8203_8206delGGAA | p.Gly2735LeufsX3 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGA | Gly | del4a | Fs. | Stop at 2737 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EB1 & hDLG binding domain (C-t |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status |
| 37_P99.09905--- | Relative |
| Symptom |
| Reference ID | Reference |
| 37 | Unpublished data |