Variant #0000756659 (NC_000007.13:g.87092143G>C, NM_000443.3:c.217C>G (ABCB4))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.87092143G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB4_000195
Frequency 11/13006
Freq. EA 11/8600
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 09:48:10 +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.217C>G r.(?) p.(Leu73Val)