Genomic variant #0000594244

Individual ID 00262572
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(32867903_33038290)_(33229611_33357493)del
DNA change (hg38) g.(32849786_33020173)_(33211494_33339376)del
Published as del ex1-2; c.(-127947_-245)_(93+1_94-1)del
ISCN -
DB-ID DMD_010102 See all 8 reported entries
Variant remarks -
Reference PubMed: Ling 2020, Journal: Ling 2020
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 +/. 0i_2i c.-244(_-182)_(59_128){0} r.? p.(fs*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000263678 DNA MLPA - - DMD 1 Chao Ling