Variant #0001489210 (NC_000016.9:g.48175235G>T, NM_033226.2:c.305C>A (ABCC12))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.48175235G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC12_000294
Frequency 2165/13002
Freq. EA 613/8600
Freq. AA 1552/4402
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 16:42:42 +02:00 (CEST)
Date last edited 2018-08-23 04:38:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC12 NM_033226.2 ?/? c.305C>A r.(?) p.(Ala102Glu)