Variant #0000603923 (NC_000011.9:g.5222877_5250289del, HBB(NM_000518.4):c.-2038_*23951del)

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.5222877_5250289del
DNA change (hg38) g.5201647_5229059del
Published as Vietnamese, SE Asian (HPFH-7, SEA-HPFH), NC_000011.10:g.5201647-5229059del27412bp
ISCN -
DB-ID HBB_004012
Variant remarks HPFH, Hb F levels
Reference IthaNet-1505
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner IthaNet - Petros Kountouris
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 +/. - c.-2038_*23951del Vietnamese, SE Asian deletion r.0 p.0