Variant #0001151858 (NC_000011.9:g.119030921C>T, NC_000011.9(NM_022169.4):c.1438-16C>T (ABCG4))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.119030921C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG4_000089
Frequency 6/12990
Freq. EA 6/8590
Freq. AA 0/4400
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 2024-12-26 17:48:30 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG4 NM_022169.4 ?/? c.1438-16C>T r.(=) p.(=)