Variant #0001070297 (NC_000011.9:g.17484956C>G, NC_000011.9(NM_000352.3):c.579+29G>C (ABCC8))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.17484956C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC8_000310
Frequency 113/12980
Freq. EA 18/8584
Freq. AA 95/4396
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 05:15:25 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ?/? c.579+29G>C r.(=) p.(=)