Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.6331T>C | p.Cys2111Arg | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TGT | Cys | CGT | Arg | T->C | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
TGFBP#06 | C in disulfide bonds 2085-2111 | No | No |
At the mRNA level | On restriction map |
NA | New restriction site(s): Mae II Lost restriction site(s): none |
Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
---|---|---|
0.67 | 0.05 (pathogenous) | 100 (Pathogenous) |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
POR01POR F0007 I0001 | Proband | Male | de novo | PORTUGAL |
Phenotypic group | Disease |
NA | MFS |
Symptom | Age |
C-Asc. aortic dilatation | 37 |
Reference ID | PubMed ID | Reference |
224 | 22005308 | Lebreiro A, Martins E, Cruz C, Almeida J, Pimenta S, Bernardes M, Carlos Machado J, Jœlia Maciel M, Abreu-Lima C. [Genotypic characterization of a Portuguese population of Marfan syndrome patients]. Rev Port Cardiol. 2011 Jul;30(7-8):649-54. |