| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1766+5G>A (1898+5G>A) | Heterozygous | Complex allele |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AGC | Ser | spl+5 | Spl. | G->A | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Mutation(s) on the other allele: c.1624G>T (p.Gly542X) |
| Other mutation(s) or variations included in a complex allele: c.2173G>A (p.Glu725Lys) |
| 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 (%) | |||||
| AAGgtatgt |
| AAGgtatat |
| -13.5 % | ||||||
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| FR001-02209-00522 | Proband | Male | Autosomal recessive |
| Phenotypic group | Disease |
| CF |
| Reference ID | Reference |
| 1 | Unpublished data |