Genomic variant #0000061559

Individual ID 00034399
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.(32519968_32536191)_(33229611_?)del
DNA change (hg38) g.(32501851_32518074)_(33211494_?)del
Published as c.-244_(2292+1_2293-1)del
ISCN -
DB-ID DMD_010018 See all 4 reported entries
Variant remarks breakpoint within 5 kb centromeric of BB (cell line GM07691B), deletion includes Dp427c
Reference PubMed: Brown 1996
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
DMD NM_004006.2 +/+ _0_18i c.-244_(2226_2293-9)del pathogenic (recessive) r.0? p.0?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000034466 DNA Southern;PCR - - DMD 1 Johan den Dunnen