The UMD-FBN1 mutations database
Record ID: 1553

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.7409G>Ap.Cys2470TyrHeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
TGCCysTACTyrG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
cb EGF-like #38 Disulfide bonds 2470-2483 (C5)NoNo

Mutation impact


At the mRNA levelOn restriction map
NANew restriction site(s): none
Lost restriction site(s): Bgl I, Nla III

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
0.670.00 (pathogenous)100 (Pathogenous)

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
ITA01FLO F0079 I01ProbandNAfamilial(51 years old)ITALIA

Phenotypic groupDisease
NAClassical MFS

Clinical data


SymptomAge
C-Asc. aortic dilatation51
S-Arm span/height >1.05 (M)51
S-Plain pes planus (M)(1)51
S-Reduced extension of the elbows (<170°)(M)(1)51
S-Scoliosis > 20° (M)(1)51
SI-Significant striae atrophicae (m)(1)51

Reference


Reference IDPubMed IDReference
14618435798
Attanasio M, Lapini I, Evangelisti L, Lucarini L, Giusti B, Porciani MC, Fattori R, Anichini C, Abbate R, Gensini GF, Pepe G. "FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations". Clin Genet. 2008 Jul;74(1):39-46.