The UMD-DMD France mutations database
Record ID: 613

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.6439_7872delp.Glu2147_Lys2624delHemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGludel1434aInFIn frame delInF

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #17 

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
 Mosaic High Normal Mosaic High
Western Blot
dys 1 dys 2 dys 3
   

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---411-0-1ProbandMaleUnknown8FRANCE

Phenotypic group
 BMD

Associated pictures


DYS I
DYS II
Myosin

Comments


+ Psychosis

Reference


Reference IDReference
1Unpublished data