| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1699A>T | p.Lys567X |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AAA | Lys | TAA | Stop | A->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Lever | Yes, non coding strand | No |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status |
| 31_H1869H1869-1H1869-1A | Relative |
| Symptom |
| Reference ID | Reference |
| 31 | Unpublished data |