Variant #0000001588 (NC_000005.10:g.148826877G>A, NM_000024.5:c.46G>A (ADRB2))

Individual ID 00000341
Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.148826877G>A
Published as -
Reference M Komara et al. (2014), dbSNP, ClinVar
DB-ID ADRB2_000002 See all 6 reported entries
dbSNP ID rs1042713
Frequency 112/160
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 2021-01-11 11:05:32 +08:00 (CST)
Date last edited 2021-09-02 09:08:22 +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     
ADRB2 NM_000024.5 -/. - c.46G>A - r.(?) p.(Gly16Arg) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000356 DNA PCR ADRB2 4 Nuur Athirah Binti Mohd Daud