The UMD-FBN1 mutations database
Record ID: 364

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.1422T>Gp.Cys474TrpHeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
TGTCysTGGTrpT->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
EGF-like #04 Disulfide bonds 460-474 (C4)NoNo

Mutation impact


At the mRNA levelOn restriction map
NANew restriction site(s): none
Lost restriction site(s): none

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

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
UKD05LON F0001 I07ProbandMalefamilial35 years oldU.K.

Phenotypic groupDisease
NAClassical MFS

Clinical data


Symptom
C-Asc. aortic dilatation
C-Asc. aortic dissection
C-Desc. aortic dissection (thor. or abdo.)
O-Ectopia lentis
O-Myopia
O-Retinal detachment
O-Strabismus
S-Arachnodactyly (M)
S-Chest deformity (unspecified)
S-High arched palate
S-Joint hypermobility (m)
SI-Significant striae atrophicae (m)(1)

Reference


Reference IDPubMed IDReference
8311748851
Comeglio P, Evans AL, Brice GW and Child AH. "Detection of six novel FBN1 mutations in british patients affected by Marfan syndrome". Human Mutation, 2001, 18(6): 546-7.