Variant #0001888632 (NC_000021.8:g.43640152T>G, NM_207174.1:c.71T>G (ABCG1))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43640152T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG1_000016
Frequency 1/12642
Freq. EA 0/8336
Freq. AA 1/4306
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 2018-08-22 23:54:13 +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.71T>G r.(?) p.(Val24Gly)