Genomic variant #0000229582

Individual ID 00138541
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
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 centrimeric breakpoint close to marker BBJ, deletion includes Dp427c
Reference PubMed: Brown
ClinVar ID -
dbSNP ID -
Origin Germline
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     
0000139381 DNA Southern;PCR - - DMD 1 Johan den Dunnen