| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.2136G>A | p.Trp712X |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| TGG | Trp | TGA | Stop | G->A | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| MLH3/PMS1/PMS2 interaction | 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_H741_H741-1_H741-1A | Relative |
| Symptom |
| Reference ID | Reference |
| 31 | Unpublished data |