The UMD-DMD France mutations database
Record ID: 2124

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS62+5G>C (c.9224+5G>C)HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
AACAsnspl+5Spl.G->CTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

Mutation impact


At the mRNA levelOn restriction map
r.[9164_9224del, 9224_9225ins9224+1_9224+62;9224+5g>c]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 (%)
Donor
CAAgtaagt
89.4 _
CAAgtaact
77.4 _ *
-13.4 %

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 No signal No signal
Western Blot
dys 1 dys 2 dys 3
 No signal No signal 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---292-6-91ProbandMaleFamilial

Phenotypic group
 DMD

Reference


Reference IDReference
106Unpublished data