The UMD-FBN1 mutations database
Record ID: 578

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS2+1G>A (c.247+1G>A)HeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
CCCProspl+1Spl.G->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
EGF-like #01 

Mutation impact


At the mRNA levelOn restriction map
Skipping of exon 2, frameshiftNew restriction site(s): none
Lost restriction site(s): none

Impact on splicing
Splice site type Wild type sequence CV Mutant type sequence CV Variation (%)
Donor
TCCgtaagt
82.3 _
TCCataagt
55.4 _ *
-32.6 %

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
USA03STA F0066 I1075ProbandNAfamilial? (32 years old)U.S.A

Phenotypic groupDisease
NAClassical MFS

Clinical data


SymptomSeverity
C-Aortic surgery
C-Asc. aortic dilatation
C-Asc. aortic dissection
C-Mitral regurgitation
O-Myopia >3 diopters (1)severe
S-Arachnodactyly (M)
S-Crowding teeth (m)
S-High arched palate
S-Joint hypermobility (m)
S-Pectus carinatum (M)(2)
S-Scoliosis > 20° (M)(1)
SI-Significant striae atrophicae (m)(1)

Reference


Reference IDPubMed IDReference
10412068374
Schrijver I, Liu W, Odom R, Brenn T, Oefner P, Furthmayr H, Francke U. "Premature termination mutations in FBN1: Distinct effects on Differencial allelic expression and on protein and clinical phenotypes". Am J Hum Genet, 2002, 71: 223-237.