Variation name (cDNA level) | Variation name (protein level) | Variation status |
c.IVS5+32C>T (c.645+32C>T) |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
CAG | Gln | spl+32 | Spl. | C>T |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
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 (%) | |||||
ACAgcgaag |
| ACAgtgaag |
| 39.2 % |
Sample ID | Patient status |
19_16325---16325.001 | Relative |
Symptom |
Reference ID | Reference |
19 | Unpublished data |