The UMD-DMD France mutations database
Record ID: 3477

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.1207G>Tp.Gly403XHemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlyTGAStopG->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #1 Yes, non coding strandNo

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
 No signal with Revertant fibers No signal with Revertant fibers No signal with Revertant fibers
Western Blot
dys 1 dys 2 dys 3
 No signal No signal 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---949-0-1ProbandMaleUnknownFRANCE

Phenotypic group
 DMD

Reference


Reference IDReference
1Unpublished data