The UMD-FBN1 mutations database
Record ID: 602

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.3302A>Gp.Tyr1101CysHeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
TATTyrTGTCysA->GTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
cb EGF-like #12 conserved AA in cbEGF-likeNoNo

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
GER03HAN F0014 I07ProbandMalede novo13 years oldGERMANY

Phenotypic groupDisease
NAClassical MFS

Clinical data


SymptomSeverity
C-Asc. aortic dilatation
O-Ectopia lentisbilateral
S-Arachnodactyly (M)
S-Dolichostenomelia
S-Increased body length
S-Scoliosis > 20° (M)(1)
SI-Significant striae atrophicae (m)(1)

Reference


Reference IDPubMed IDReference
10712402346
Rommel K, Karck M, Haverich A, Schmidtke J, Arslan-Kirchner M. "Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations". Hum Mutat. 2002 Nov;20(5):406-7.