Variant #0000000161 (NC_000011.10:g.5226970T>A, NM_000518.4:c.52A>T (HBB))

Individual ID 00000028
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5226970T>A
Published as -
Reference Hassan S et al. 2013dbSNP
DB-ID HBB_000011 See all 21 reported entries
dbSNP ID rs33986703
Frequency 3/169
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2018-12-26 16:23:45 +08:00 (CST)
Date last edited 2021-08-18 12:43:34 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
HBB NM_000518.4 +/. - c.52A>T - r.(?) p.(Lys18*) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000040 DNA PCRm HBB 12 MyHVP