Variant #0000442357 (NC_000003.11:g.183689456G>C, NM_005688.2:c.1656C>G (ABCC5))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.183689456G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC5_000148
Frequency 2/12732
Freq. EA 0/8482
Freq. AA 2/4250
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 07:20:57 +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.1656C>G r.(?) p.(Asp552Glu)