Genomic variant #0000594133

Individual ID 00262461
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.(33038290_33229611)_(33229611_33357493)del
DNA change (hg38) g.(33020173_33211494)_(33211494_33339376)del
Published as del ex1; c.(-127947_-245)_(31+1_32-1)del
ISCN -
DB-ID DMD_046507
Variant remarks -
Reference Ling 2019, submitted
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Chao Ling




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
DMD NM_004006.2 +/. 0i_1i c.-244(_-182)_(-182_59)del pathogenic (recessive) r.? p.(fs*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000263567 DNA MLPA - - DMD 1 Chao Ling