Variant #0000320057 (NC_000002.11:g.220078496T>C, NC_000002.11(NM_005689.2):c.1578+52A>G (ABCB6))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.220078496T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB6_000095
Frequency 5605/5734
Freq. EA 3978/3982
Freq. AA 1627/1752
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 22:04:12 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB6 NM_005689.2 ?/? c.1578+52A>G r.(=) p.(=)