Variant #0001257866 (NC_000012.11:g.123444507G>T, NM_019624.3:c.276C>A (ABCB9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.123444507G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB9_000139
Frequency 148/13006
Freq. EA 134/8600
Freq. AA 14/4406
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 16:39:18 +02:00 (CEST)
Date last edited 2018-08-23 09:52:57 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB9 NM_019624.3 ?/? c.276C>A r.(?) p.(Phe92Leu)