The UMD-DMD France mutations database
Record ID: 1634

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.6291_8938dupp.Leu2981IlefsX2HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GGGGlyins2647cFs.Stop at 2982Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #16 

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 Medium Mosaic Medium
Western Blot
dys 1 dys 2 dys 3
  Increased size, abnormal quantity (500 kDa) 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---015-8-81ProbandMaleFamilialFRANCE

Phenotypic group
 BMD

Comments


see also Ref 118 Somatic mosaïcism : presence of both the 427 kDa and 500 kDa bands on Western blots

Reference


Reference IDReference
106Unpublished data