Variant #0000286100 (NC_000002.11:g.169850388T>C, NM_003742.2:c.616A>G (ABCB11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.169850388T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB11_000192
Frequency 32/11878
Freq. EA 0/8178
Freq. AA 32/3700
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 00:13:29 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB11 NM_003742.2 ?/? c.616A>G r.(?) p.(Ile206Val)