The UMD-DMD France mutations database
Record ID: 1912

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.3787_6438delp.Glu1263_Lys2146delHemizygous

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGludel2652aInFIn frame delInF

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #8 

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
---050-7-m011ProbandMaleFamilial

Phenotypic group
 DMD

Comments


Immunofluorescence : low signal

Reference


Reference IDReference
113Unpublished data