Variant #0000602642 (NC_000011.9:g.5247871_5248779del, HBB(NM_000518.4):c.-528_251del)

Individual ID 00268821
Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.5247871_5248779del
DNA change (hg38) g.5226641_5227549del
Published as -
ISCN -
DB-ID HBB_001678 See all 2 reported entries
Variant remarks Afghan deletion beta0 (909 bp del)
Reference data from Globin Gene Server (HbVar-2738), Old J (E-5816-2010), PubMed: Gallienne AE
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner HbVar - Belinda Giardine and Ross Hardison
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 +?/. _1_2 c.-528_251del Afghan deletion beta0 r.0? p.0?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000269950 DNA ? - - HBB 1 HbVar - Belinda Giardine and Ross Hardison