The UMD-FBN1 mutations database
Record ID: 1486

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.640G>Ap.Gly214SerHeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GGCGlyAGCSerG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Hybrid module#01 Yes, non coding strandYes

Mutation impact


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

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
0.670.00 (pathogenous)76 (Pathogenous)

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
ITA01FLO F0016 I01ProbandNAde novoITALIA

Phenotypic groupDisease
NAClassical MFS

Clinical data


SymptomAge
C-Asc. aortic dilatation27
C-Mitral valve prolapse27
O-Ectopia lentis27
S-Arachnodactyly (M)27
S-Arm span/height >1.05 (M)27
S-Reduced extension of the elbows (<170°)(M)(1)27

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.