The UMD-DMD France mutations database
Record ID: 2536

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS60-1G>A (c.9085-1G>A)HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValspl-1Spl.G->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

Mutation impact


At the mRNA levelOn restriction map
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 (%)
Acceptor
ttttcctcccagGT
98.5 _
ttttcctcccaaGT
69.5 _ *
-29.4 %

On isoforms (a blue cell indicates that the corresponding isoform is affected by the mutation)
Dp 427cDp 427mDp 427pDp 260Dp 140Dp 116Dp 71
       
Immunofluorescence
dys 1 dys 2 dys 3
  No signal 
Western Blot
dys 1 dys 2 dys 3
   

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---449-2-11ProbandMaleFamilialPANAMA

Phenotypic group
 DMD

Reference


Reference IDReference
106Unpublished data