The UMD-FBN1 mutations database
Record ID: 217

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS30+28C>A (c.3838+28C>A)HeterozygousPolymorphism?

wt codonwt aamutant codonmutant aamutational eventmutation type
GATAspspl+28Spl.C->ATv

StructureKey Residue (HCD)Pyrimidin doubletCpG
cb EGF-like #17 Ca2+ binding

Mutation impact


At the mRNA levelOn restriction map
Not tested on cDNA (needed)New restriction site(s): none
Lost restriction site(s): none

Impact on splicing
Splice site type Wild type sequence CV Mutant type sequence CV Variation (%)

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
USA08PIT F0011 I01ProbandNANA?U.S.A

Phenotypic groupDisease
NAClassical MFS

Clinical data


Symptom
no clinical data

Reference


Reference IDPubMed IDReference
4910533071
Yuan B, Thomas JP, von Kodolitsch Y, Pyeritz RE. "Comparison of heteroduplex analysis, direct sequencing, and enzyme mismatch cleavage for detecting mutations in a large gene, FBN1". Hum Mutat 1999;14(5):440-6 .