The UMD-DMD France mutations database
Record ID: 18432

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS65-427T>G (c.9564-427T>G)Mutation

wt codonwt aamutant codonmutant aamutational eventmutation type
ACGThrspl-427Spl.T->GTv

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 (%)
Cryptic Acceptor?
GTTGCTGGTAATTTT
42.9 _
GTTGCTGGTAAGTTT
71.9 _ *
40.3 %

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
   
Western Blot
dys 1 dys 2 dys 3
   

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---MD_CZ_SK#DMD-080930M-SHProbandMCZ

Phenotypic group
 

Reference


Reference IDReference
0Unpublished data