Variant #0000756887 (NC_000007.13:g.87199564C>A, NC_000007.13(NM_000927.4):c.287-25G>T (ABCB1))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.87199564C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB1_000212
Frequency 3207/13004
Freq. EA 1694/8598
Freq. AA 1513/4406
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 02:10:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB1 NM_000927.4 ?/? c.287-25G>T r.(=) p.(=)