Variant #0001070332 (NC_000011.9:g.17498342T>C, NM_000352.3:c.-19A>G (ABCC8))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.17498342T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC8_000345
Frequency 166/12340
Freq. EA 3/8148
Freq. AA 163/4192
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 16:37:25 +02:00 (CEST)
Date last edited 2018-08-23 11:12:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ?/? c.-19A>G r.(=) p.(=)