The UMD-DMD France mutations database
Record ID: 3454

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS64+5G>C (c.9361+5G>C)HemizygousMutation

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

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

Mutation impact


At the mRNA levelOn restriction map
2 RNAs: normal + in frame insertion of 57 nucleotides (57 first nucleotides of iNew 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
GCTgtaagt
82.6 _
GCTgtaact
70.6 _ *
-14.5 %

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
 Irregular Medium Irregular Medium Irregular Medium
Western Blot
dys 1 dys 2 dys 3
 Reduced size, low quantity Reduced size, low quantity Reduced size, low quantity

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---966-0-1ProbandMaleFamilialSPAIN

Phenotypic group
 BMD

Reference


Reference IDReference
1Unpublished data