Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.3463G>A | p.Asp1155Asn | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
GAC | Asp | AAC | Asn | G->A | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
cb EGF-like #14 | Ca2+ binding | Yes, non coding strand | Yes |
At the mRNA level | On restriction map |
Last nucleotide of the exon, no abnormal splicing | New restriction site(s): none Lost restriction site(s): Taq I |
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 |
AUS02WES F0011 I01 | Proband | NA | NA | ? (15 years old) | AUSTRALIA |
Phenotypic group | Disease |
NA | Classical MFS |
Symptom |
C-Asc. aortic dilatation |
S-Characteristic facial appearance |
S-Crowding teeth (m) |
S-High arched palate |
S-Joint hypermobility (m) |
S-Pectus excavatum severe |
S-Plain pes planus (M)(1) |
S-Reduced US/LS ratio <0.87 (M) |
SI-Inguinal hernia |
SI-Significant striae atrophicae (m)(1) |
Reference ID | PubMed ID | Reference |
114 | 14695540 | Biggin A, Holman K, Brett M, Bennetts B, Ades L. "Detection of thirty novel FBN1 mutations in patients with Marfan syndrome or a related fibrillinopathy". Hum Mutat. 2004 Jan;23(1):99. |