Variant #0000002876 (NC_000011.10:g.5226929C>T, NC_000011.10(NM_000518.4):c.92+1G>A (HBB))

Individual ID 00000694
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5226929C>T
Published as -
Reference Jin-Ai M A Tan et al.(2014)dbSNP
DB-ID HBB_000013 See all 5 reported entries
dbSNP ID rs33971440
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-06-23 14:05:37 +08:00 (CST)
Date last edited 2021-08-18 14:11:44 +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 +/. 1i c.92+1G>A IVS1-1(G>A) r.spl? p.? - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000764 DNA PCRm;SEQ HBB 2 Nur Aisyah Athirah