Variant #0000001590 (NC_000005.10:g.148826910G>C, ADRB2(NM_000024.5):c.79G>C)

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.148826910G>C
Published as -
Reference M Komara et al. (2014), dbSNP, (OMIM 0002), ClinVar
DB-ID ADRB2_000001 See all 5 reported entries
dbSNP ID rs1042714
Frequency 80/160
Variant remarks -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
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
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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.79G>C - r.(?) p.(Glu27Gln) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000356 DNA PCR ADRB2 4 Nuur Athirah Binti Mohd Daud