Variant #0000001858 (NC_000011.10:g.5226943C>T, NM_000518.4:c.79G>A (HBB))

Individual ID 00000400
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5226943C>T
Published as CD 26 GAG>AAG / HbE
Reference dbSNP, (OMIM 0071), ClinVar
DB-ID HBB_000006 See all 40 reported entries
dbSNP ID rs33950507
Frequency 11/28
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-02-07 15:25:09 +08:00 (CST)
Date last edited 2021-08-18 14:53:39 +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 +/. 1 c.79G>A CD 26 GAG>AAG / HbE r.(?) p.(Glu27Lys) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000414 DNA PCR HBB 5 Nuur Athirah Binti Mohd Daud