| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1331A>G | p.Asn444Ser |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AAT | Asn | AGT | Ser | A->G | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EXO1 interaction | Yes, non 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) |
|---|---|---|
| 0.64 | 0.67 (non pathogenous) | 41 (Polymorphism) |
| Sample ID | Patient status |
| 31_H1696H16962H16962A | Relative |
| Symptom |
| Reference ID | Reference |
| 31 | Unpublished data |