The UMD-DMD France mutations database
Record ID: 310

Mutation description

Variation name (cDNA level)	Variation name (protein level)	Variation status	Variation class
c.6913_7309del	p.Val2305LeufsX9	Hemizygous	Mutation

wt codon	wt aa	mutant codon	mutant aa	mutational event	mutation type
GTT	Val	del397a	Fs.	Stop at 2313	Fr.

Structure	Key Residue (HCD)	Pyrimidin doublet	CpG
CRD-repeat #18

Mutation impact

At the mRNA level	On 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 427c	Dp 427m	Dp 427p	Dp 260	Dp 140	Dp 116	Dp 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 ID	Patient status	Gender	Transmission	Age of onset	Age of death	Geographic origin
---503-0-1	Proband	Male	De novo	5		FRANCE

Phenotypic group

DMD

Associated pictures

Comments

+ Mental retardation

Reference

Reference ID	Reference
1	Unpublished data