Variant #0000003463 (NC_000011.10:g.5225488A>G, NM_000518.4:c.*110T>C (HBB))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5225488A>G
Published as -
Reference dbSNP, ClinVar
DB-ID HBB_000034 See all 4 reported entries
dbSNP ID rs33978907
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Noorzalifah Binti Mazuki
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Noorzalifah Binti Mazuki
Date created 2021-09-27 10:18:42 +08:00 (CST)
Date last edited 2022-03-13 10:36:56 +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.*110T>C Poly A (A>G) r.(=) p.(=) - ClinVar



Screenings

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