Variant #0001489237 (NC_000016.9:g.48180206T>G, NC_000016.9(NM_033226.2):c.119+11A>C (ABCC12))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.48180206T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC12_000321
Frequency 12/13002
Freq. EA 12/8600
Freq. AA 0/4402
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 00:59:13 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC12 NM_033226.2 ?/? c.119+11A>C r.(=) p.(=)