Variant #0000286093 (NC_000002.11:g.169847417C>A, NM_003742.2:c.802G>T (ABCB11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.169847417C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB11_000178
Frequency 1/11968
Freq. EA 1/8224
Freq. AA 0/3744
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 16:22:05 +02:00 (CEST)
Date last edited 2018-08-23 12:37:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB11 NM_003742.2 ?/? c.802G>T r.(?) p.(Asp268Tyr)