Variation name (cDNA level) | Variation name (protein level) | Variation status |
c.1327dup | p.Glu443GlyfsX17 |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
GAA | Glu | ins1b | Fs. | Stop at 459 |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
At the mRNA level | On restriction map |
New restriction site(s): none Lost restriction site(s): none |
Sample ID | Patient status |
SO_-2273G03153G03153 | Relative |
Symptom |
Reference ID | Reference |
71 | Unpublished data |