The UMD-DMD France mutations database
Record ID: 210

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.3433_6290delp.Val1145AlafsX3HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GTCValdel2858aFs.Stop at 1147Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #7 

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

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
---239-0-1ProbandMaleFamilial

Phenotypic group
 DMD

Reference


Reference IDReference
1Unpublished data