Genomic variant #0000229466

Individual ID 00138426
Chromosome X
Allele Parent #1
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 del1b-18; c.-244_(2292+1_2293-1)del
ISCN -
DB-ID DMD_010018 See all 4 reported entries
Variant remarks -
Reference PubMed: Kalman 2011
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     
0000139266 DNA arraySNP;MLPA - - DMD 1 Johan den Dunnen