Variant #0000603575 (NC_000011.9:g.5247988_5247996del, HBB(NM_000518.4):c.131_139del)

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.5247988_5247996del
DNA change (hg38) g.5226758_5226766del
Published as CD 42-45 (-9bp), 130_138delGAGTCCTTT
ISCN -
DB-ID HBB_001062 See all 2 reported entries
Variant remarks β-chain variant, Haemolytic anaemia
Reference IthaNet-946
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner IthaNet - Petros Kountouris
Database submission license No license selected
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 +/. - c.131_139del Hb Niteroi r.(?) p.(Glu44_Phe46del)