The UMD-DMD France mutations database
Record ID: 629

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.6913_8937delp.Val2305_Lys2979delHemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GTTValdel2025aInFIn frame delInF

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #18 

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
---354-0-1ProbandMaleUnknown36

Phenotypic group
 BMD

Reference


Reference IDReference
1Unpublished data