Variant #0000000366 (NC_000011.9:g.5248200T>A, HBB(NM_000518.4):c.52A>T)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.5248200T>A
Reference (OMIM 0311);dbSNP;Chang JC et al.;
DB-ID HBB_000047 See all 2 reported entries
Frequency -
Variant remarks Codon 17 (A->T); AAG(Lys)->TAG(stop codon) beta0
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 c.52A>T r.(?) p.(Lys18*)