| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1045C>G | p.Pro349Ala |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CCT | Pro | GCT | Ala | C->G | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EXO1 stabilization | Yes, coding strand | 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 | 0.00 (pathogenous) | 71 (Probably pathogenous) |
| Sample ID | Patient status |
| 41_HNPCC463_HNPCC463001_2 | Relative |
| Symptom |
| Reference ID | Reference |
| 41 | Unpublished data |