The UMD-DMD France mutations database
Record ID: 2388

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.7310_7542delp.Ser2437CysfsX33HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
TCTSerdel233bFs.Stop at 2469Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-hinge region #3 

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
  No signal No signal

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---333-7-51ProbandMaleUnknownITALIA

Phenotypic group
 DMD

Reference


Reference IDReference
106Unpublished data