Variant #0000442359 (NC_000003.11:g.183689586G>A, NM_005688.2:c.1526C>T (ABCC5))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.183689586G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC5_000153
Frequency 4/12226
Freq. EA 4/8294
Freq. AA 0/3932
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 11:10:57 +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.1526C>T r.(?) p.(Ser509Leu)