Variant #0001888692 (NC_000021.8:g.43702563G>A, NC_000021.8(NM_207174.1):c.767+34G>A (ABCG1))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43702563G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG1_000076
Frequency 189/13004
Freq. EA 3/8600
Freq. AA 186/4404
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 01:53:02 +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.767+34G>A r.(=) p.(=)