Variant #0000000278 (NC_000022.10:g.17690423G>A, NM_001282225.2:c.145C>T (ADA2))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.17690423G>A
Reference -
DB-ID ADA2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-28 12:57:36 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADA2 NM_001282225.2 +/+ - c.145C>T r.(?) p.(Arg49Trp)