Variant #0001974687 (NC_000023.10:g.74284997G>A, NM_004299.3:c.1742C>T (ABCB7))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.74284997G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB7_000022
Frequency 1087/10563
Freq. EA 8/6728
Freq. AA 1079/3835
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 16:50:35 +02:00 (CEST)
Date last edited 2018-08-23 02:10:10 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB7 NM_004299.3 ?/? c.1742C>T r.(?) p.(Ala581Val)