The UMD-DMD France mutations database
Record ID: 1295

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS26+3insT (c.3603+3insT)HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
AAGLysspl+3Spl.insTTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

Mutation impact


At the mRNA levelOn restriction map
r.[=, 3603_3604ins3603+1_3603+117;3603+2dup]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
AAGgtaaaa
99.7 _
AAGgttaaa
81.8 _ *
-17.9 %

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
 Normal size, medium quantity Normal size, medium quantity 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---038-0-1ProbandMaleDe novo

Phenotypic group
 BMD

Associated pictures


DYS I
DYS II
Myosine

Reference


Reference IDPubMed IDReference
1017041906
Deburgrave N, Daoud F, Llense S, Barbot JC, R*can D, Peccate C, Burghes AH, B*roud C, Garcia L, Kaplan JC, Chelly J, Leturcq F. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene. Hum Mutat. 2007 Feb;28(2):183-95.