Variant #0000000318 (NC_000011.9:g.5246909_5268823del, HBB(NM_000518.4):c.-20572_363del)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5246909_5268823del
Reference Shang et al
DB-ID HBD_000027 See all 2 reported entries
Frequency -
Variant remarks 21.9k del
ClassClinical Pathogenic
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBB NM_000518.4 ./. 01-03 c.-20572_363del r.? p.?