Variant #0000756598 (NC_000007.13:g.87069613C>G, NM_000443.3:c.1462G>C (ABCB4))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.87069613C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB4_000134
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 16:28:58 +02:00 (CEST)
Date last edited 2018-08-23 10:32:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB4 NM_000443.3 ?/? c.1462G>C r.(?) p.(Glu488Gln)