The UMD-FBN1 mutations database
Record ID: 2151

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.5096A>Gp.Tyr1699CysHeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
TACTyrTGCCysA->GTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
TGFBP#05 NoNo

Mutation impact


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

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
10.01 (pathogenous)82 (Pathogenous)

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
FRA02PAR F0008 I0001ProbandNANASWITZERLAND

Phenotypic groupDisease
NAGeleophysic dysplasia

Clinical data


SymptomSeverityAge
C-Aortic insufficiencymild21

Reference


Reference IDPubMed IDReference
20021683322
Le Goff C, Mahaut C, Wang LW, Allali S, Abhyankar A, Jensen S, Zylberberg L, Collod-Beroud G, Bonnet D, Alanay Y, Brady AF, Cordier MP, Devriendt K, Genevieve D, Kiper P…, Kitoh H, Krakow D, Lynch SA, Le Merrer M, M*garbane A, Mortier G, Odent S, Polak M, Rohrbach M, Sillence D, Stolte-Dijkstra I, Superti-Furga A, Rimoin DL, Topouchian V, Unger S, Zabel B, Bole-Feysot C, Nitschke P, Handford P, Casanova JL, Boileau C, Apte SS, Munnich A, Cormier-Daire V. "Mutations in the TGF-beta binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias". Am J Hum Genet. 2011 Jul 15;89(1):7-14.