Variant #0000286113 (NC_000002.11:g.169853118T>G, NC_000002.11(NM_003742.2):c.477+27A>C (ABCB11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.169853118T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB11_000198
Frequency 4/11872
Freq. EA 0/8164
Freq. AA 4/3708
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 2024-04-27 14:01:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB11 NM_003742.2 ?/? c.477+27A>C r.(=) p.(=)