Variant #0000803582 (NC_000007.13:g.150731698C>T, NC_000007.13(NM_007188.3):c.659+12C>T (ABCB8))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.150731698C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB8_000064
Frequency 1370/13006
Freq. EA 995/8600
Freq. AA 375/4406
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 16:28:58 +02:00 (CEST)
Date last edited 2018-08-23 00:19:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB8 NM_007188.3 ?/? c.659+12C>T r.(=) p.(=)