Variation name (cDNA level) | Variation name (protein level) | Variation status |
c.117_545del | p.Cys39_Arg182delinsTrp |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TGT | Cys | del429c | InF | In frame del | InF |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
ATPase |
At the mRNA level | On restriction map |
New restriction site(s): none Lost restriction site(s): none |
Sample ID | Patient status |
19_7725_7725-006_7725-006 | Relative |
Symptom |
Reference ID | Reference |
19 | Unpublished data |