Variant #0000803529 (NC_000007.13:g.150725722A>C, NC_000007.13(NM_007188.3):c.95+25A>C (ABCB8))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.150725722A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB8_000011
Frequency 5314/12998
Freq. EA 3062/8598
Freq. AA 2252/4400
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 11:22:07 +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.95+25A>C r.(=) p.(=)