| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.IVS15+5G>C (c.2634+5G>C) |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAG | Glu | spl+5 | Spl. | G>C |
| 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 (%) | |||||
| GAGgtttgt |
| GAGgtttct |
| -14.2 % | ||||||
| Sample ID | Patient status |
| 31_H1006_H1006-1_H1006-1A | Relative |
| Symptom |
| Reference ID | Reference |
| 31 | Unpublished data |