Variant #0001257808 (NC_000012.11:g.123430646G>A, NM_019624.3:c.1177C>T (ABCB9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.123430646G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB9_000081
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 10:59:48 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB9 NM_019624.3 ?/? c.1177C>T r.(?) p.(Arg393Trp)