Variant #0000286114 (NC_000002.11:g.169853122A>C, NC_000002.11(NM_003742.2):c.477+23T>G (ABCB11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.169853122A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB11_000199
Frequency 1/11878
Freq. EA 1/8168
Freq. AA 0/3710
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 04:39:28 +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.477+23T>G r.(=) p.(=)