Variant #0000320061 (NC_000002.11:g.220078589A>G, NM_005689.2:c.1537T>C (ABCB6))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.220078589A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB6_000099
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 16:22:05 +02:00 (CEST)
Date last edited 2025-01-02 20:21:10 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB6 NM_005689.2 ?/? c.1537T>C r.(?) p.(Ser513Pro)