The UMD-FBN1 mutations database
Record ID: 3204

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
CAN02VAN F0001 I0004RelativeMalefamilialCANADA

Phenotypic groupDisease
NAMFS

Clinical data


Symptom
C-Asc. aortic dilatation
CF-Down-slanting palpebral fissures
S-Arm span/height >1.05 (M)
S-High arched palate
S-Reduced US/LS ratio <0.87 (M)

Reference


Reference IDPubMed IDReference
25423653584
Potter KJ, Creighton S, Armstrong L, Eydoux P, Duncan W, Penny DJ, Fan Y, Gibson WT. "The c.7409G>A (p.Cys2470Tyr) Variant of FBN1: Phenotypic Variability across Three Generations". Mol Syndromol. 2013 Mar;4(3):125-35.