The UMD-DMD France mutations database
Record ID: 3554

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.IVS40-2A>G (c.5740-2A>G)HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGluspl-2Spl.A->GTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

Mutation impact


At the mRNA levelOn restriction map
r.[=, 5740_5922del]New restriction site(s): none
Lost restriction site(s): none

Impact on splicing
Splice site type Wild type sequence CV Mutant type sequence CV Variation (%)
Acceptor
tttgctcaatagGA
83.9 _
tttgctcaatggGA
55 _ *
-34.5 %

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
 Normal Irregular Medium Irregular High
Western Blot
dys 1 dys 2 dys 3
 Normal size, medium quantity Normal size, medium quantity 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---977-0-1ProbandMaleFamilialFRANCE

Phenotypic group
 BMD

Reference


Reference IDReference
1Unpublished data