Variant #0001070334 (NC_000011.9:g.17498372C>G, NM_000352.3:c.-49G>C (ABCC8))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.17498372C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC8_000347
Frequency 142/9526
Freq. EA 5/6302
Freq. AA 137/3224
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 00:52:32 +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.-49G>C r.(=) p.(=)