Genomic variant #0000233590

Individual ID 00142570
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.(32663242_32716088)_(33229611_?)dup
DNA change (hg38) g.(32645125_32697971)_(33211494_?)dup
Published as ex1ex9dup; c.-244_(960+1_961-1)dup
ISCN -
DB-ID DMD_020009
Variant remarks -
Reference -
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 Alessandra Ferlini




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
DMD NM_004006.2 +/. _0_9i c.-244_(859_988)dup pathogenic (recessive) r.(?) p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000143410 DNA MLPA - - DMD 1 Alessandra Ferlini