Variant #0001151801 (NC_000011.9:g.119025546del, NM_022169.4:c.607del (ABCG4))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.119025546del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG4_000032
Frequency 132/12518
Freq. EA 83/8254
Freq. AA 49/4264
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 12:33:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG4 NM_022169.4 ?/? c.607del r.(?) p.(Gly203Alafs*41)