| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1698T>C | p.Asn566Asn |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AAT | Asn | AAC | Asn | T->C | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EXO1 stabilization | No | No |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 1 | 0.32 (non pathogenous) | 18 (Polymorphism) |
| Sample ID | Patient status |
| 5_2004007_P0024538_AAA051 | Relative |
| Symptom |
| Reference ID | Reference |
| 5 | Unpublished data |