Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.719G>A | p.Arg240His | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
CGC | Arg | CAC | His | G->A | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
Hybrid module#01 | No | Yes |
At the mRNA level | On restriction map |
NA | New restriction site(s): none Lost restriction site(s): none |
Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
---|---|---|
0.67 | 0.00 (pathogenous) | 59 (Probable polymorphism) |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
NET04NIJ F0003 I0001 | Proband | Female | familial | NETHERLAND |
Phenotypic group | Disease |
NA | Classical MFS |
Symptom | Severity | Age |
CNS-Lumbosacral dural ectasia | 18 | |
O-Ectopia lentis | bilateral | 14 |
S-Arachnodactyly (M) | 18 | |
S-Arm span/height >1.05 (M) | moderate =1,05 | 18 |
S-Kyphosis | 18 | |
S-Pectus excavatum severe | 18 | |
S-Scoliosis > 20° (M)(1) | 18 |
Reference ID | PubMed ID | Reference |
184 | 19059503 | Van Dijk FS, Hamel BC, Hilhorst-Hofstee Y, Mulder BJ, Timmermans J, Pals G, Cobben JM. "Compound-heterozygous Marfan syndrome". Eur J Med Genet. 2009 Jan-Feb;52(1):1-5. |