Variant #0001888669 (NC_000021.8:g.43693582C>A, NC_000021.8(NM_207174.1):c.570+37C>A (ABCG1))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43693582C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG1_000053
Frequency 1/12914
Freq. EA 0/8588
Freq. AA 1/4326
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 16:49:50 +02:00 (CEST)
Date last edited 2018-08-23 09:08:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG1 NM_207174.1 ?/? c.570+37C>A r.(=) p.(=)