Variation name (cDNA level) | Variation name (protein level) | Variation status |
c.5354_5359del | p.Tyr1785_Thr1787delinsSer |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TAT | Tyr | del6b | InF | In frame del | InF |
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_-157G02570G02570 | Relative |
Symptom |
Reference ID | Reference |
71 | Unpublished data |