Variant #0001489235 (NC_000016.9:g.48180198T>C, NC_000016.9(NM_033226.2):c.119+19A>G (ABCC12))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.48180198T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC12_000319
Frequency 461/13002
Freq. EA 7/8600
Freq. AA 454/4402
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 09:12:24 +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.119+19A>G r.(=) p.(=)