Variant #0000320142 (NC_000002.11:g.220082906C>T, NM_005689.2:c.490G>A (ABCB6))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.220082906C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB6_000180
Frequency 9/13006
Freq. EA 3/8600
Freq. AA 6/4406
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 16:22:05 +02:00 (CEST)
Date last edited 2025-01-02 20:39:24 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB6 NM_005689.2 ?/? c.490G>A r.(?) p.(Ala164Thr)