Variant #0001151834 (NC_000011.9:g.119028957T>C, NM_022169.4:c.1082T>C (ABCG4))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.119028957T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG4_000065
Frequency 1/12990
Freq. EA 1/8590
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 2018-08-23 09:33:02 +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.1082T>C r.(?) p.(Ile361Thr)