The UMD-DMD France mutations database
Record ID: 3179

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.3433_4233delp.Val1145_Gln1411delHemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GTCValdel801aInFIn frame delInF

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #7 

Mutation impact


At the mRNA levelOn restriction map
del exon 26-30New 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 Normal Irregular Medium
Western Blot
dys 1 dys 2 dys 3
 No signal Reduced size, medium quantity 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---771-0-1ProbandMaleFamilialSPAIN

Phenotypic group
 BMD

Reference


Reference IDReference
1Unpublished data