Genomic variant #0000604069

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.5248228dup
DNA change (hg38) g.5226998dup
Published as CD 7/8 (+G)
ISCN -
DB-ID HBB_001881 See all 2 reported entries
Variant remarks β-thalassaemia
Reference IthaNet-2958
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner IthaNet - Petros Kountouris
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     
HBB NM_000518.4 +/. - c.24dup - pathogenic r.(?) p.(Lys9Glufs*15)