Variant #0000000264 (NC_000011.10:g.5226929C>A, NC_000011.10(NM_000518.4):c.92+1G>T (HBB))

Individual ID 00000055
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5226929C>A
Published as IVS I-1 (G>T)
Reference E George et al. (1992), dbSNP, (OMIM 0347), ClinVar
DB-ID HBB_000004 See all 25 reported entries
dbSNP ID rs33971440
Frequency 9/141
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 2020-10-18 08:48:04 +08:00 (CST)
Date last edited 2021-08-19 10:40:08 +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>T IVS I-1 (G>T) r.spl? p.? - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000068 DNA PCRm HBB 12 Nuur Athirah Binti Mohd Daud