Variant #0000442382 (NC_000003.11:g.183700349G>A, NM_005688.2:c.889C>T (ABCC5))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.183700349G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC5_000182
Frequency 3/11992
Freq. EA 3/8230
Freq. AA 0/3762
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 16:23:53 +02:00 (CEST)
Date last edited 2018-08-23 08:56:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC5 NM_005688.2 ?/? c.889C>T r.(=) p.(=)