The UMD-DMD France mutations database
Record ID: 2909

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class

wt codonwt aamutant codonmutant aamutational eventmutation type

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

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
Relative

Phenotypic group
 

Reference


Reference IDReference
0Unpublished data