The UMD-DMD France mutations database
Record ID: 41

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.39delAp.Glu14LysfsX12

wt codonwt aamutant codonmutant aamutational eventmutation type
AGAArgdel1cFs.Stop at 25Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Actin binding domain 

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
---EAT_NMD_AR#AHGD15ProbandMAR

Phenotypic group
 

Reference


Reference IDReference
0Unpublished data