Variant #0000921428 (NC_000009.11:g.107620867C>T, NM_005502.3:c.656G>A (ABCA1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.107620867C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA1_000400
Frequency 5092/13006
Freq. EA 2420/8600
Freq. AA 2672/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:58 +02:00 (CEST)
Date last edited 2019-03-01 01:14:24 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA1 NM_005502.3 ?/? c.656G>A r.(?) p.(Arg219Lys)