Variant #0000756848 (NC_000007.13:g.87180198C>T, NC_000007.13(NM_000927.4):c.1000-44G>A (ABCB1))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.87180198C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB1_000173
Frequency 8098/12998
Freq. EA 4898/8598
Freq. AA 3200/4400
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 07:28:05 +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.1000-44G>A r.(=) p.(=)