Variant #0001151865 (NC_000011.9:g.119031129G>T, NC_000011.9(NM_022169.4):c.1596+34G>T (ABCG4))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.119031129G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG4_000096
Frequency 56/12990
Freq. EA 50/8590
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 2018-08-23 04:32:08 +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.1596+34G>T r.(=) p.(=)