Variation name (cDNA level) | Variation name (protein level) | Variation status |
c.IVS8-119C>G (c.934-119C>G) |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
GTG | Val | spl-119 | C>G |
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 (%) | |||||
Sample ID | Patient status |
19_24119---24119-001 | Relative |
Symptom |
Reference ID | Reference |
19 | Unpublished data |