Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.2456G>A | p.Gly819Glu | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
GGA | Gly | GAA | Glu | G->A | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
cb EGF-like #09 | conserved AA in cbEGF-like | Yes, non coding strand | No |
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) | 100 (Pathogenous) |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
FRA03MON F0231 I0001 | Proband | Male | familial | FRANCE |
Phenotypic group | Disease |
NA | Classical MFS |
Symptom | Age |
C-Asc. aortic dissection | 40 |
S-Arachnodactyly (M) | 59 |
S-Crowding teeth (m) | 59 |
S-High arched palate | 59 |
S-Joint hypermobility (m) | 59 |
S-Pectus excavatum moderate (m)(1) | 59 |
S-Protusio acetabulæ (M)(2) | 59 |
S-Reduced extension of the elbows (<170°)(M)(1) | 59 |
S-Reduced US/LS ratio <0.87 (M) | 59 |
SI-Inguinal hernia | 59 |
Reference ID | PubMed ID | Reference |
191 | 19802897 | Khau Van Kien P, Baux D, Pallares-Ruiz N, Baudoin C, Plancke A, Chassaing N, Collignon P, Drouin-Garraud V, Hovnanian A, Martin-Coignard D, Collod-B*roud G, B*roud C, Roux AF, Claustres M. "Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domains". Hum Mutat. 2010 Jan;31(1):E1021-42. |