Variant #0000286084 (NC_000002.11:g.169842809T>C, NC_000002.11(NM_003742.2):c.909-15A>G (ABCB11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.169842809T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB11_000169
Frequency 8789/11884
Freq. EA 5686/8190
Freq. AA 3103/3694
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 2024-04-22 23:28:52 +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.909-15A>G r.(=) p.(=)