Variant #0001151845 (NC_000011.9:g.119029342G>A, NM_022169.4:c.1243G>A (ABCG4))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.119029342G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG4_000076
Frequency 6/12990
Freq. EA 0/8590
Freq. AA 6/4400
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 16:37:25 +02:00 (CEST)
Date last edited 2018-08-22 23:50:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG4 NM_022169.4 ?/? c.1243G>A r.(?) p.(Asp415Asn)