Variant #0000286156 (NC_000002.11:g.169874671T>C, NC_000002.11(NM_003742.2):c.-27-9A>G (ABCB11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.169874671T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB11_000241
Frequency 1/11788
Freq. EA 0/8170
Freq. AA 1/3618
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 03:35:48 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB11 NM_003742.2 ?/? c.-27-9A>G r.(=) p.(=)