| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.IVS7+51C>A (c.1276+51C>A) |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGA | Gly | spl+51 | Spl. | C>A | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| MSH3/MSH6 interaction |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Impact on splicing | ||||||||||
| Splice site type | Wild type sequence | CV | Mutant type sequence | CV | Variation (%) | |||||
| Sample ID | Patient status |
| 2_02-ACT3042_19355_19355 | Relative |
| Symptom |
| Reference ID | Reference |
| 2 | Unpublished data |