Variant #0001070292 (NC_000011.9:g.17483342C>T, NM_000352.3:c.610G>A (ABCC8))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.17483342C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC8_000305
Frequency 1/12986
Freq. EA 0/8586
Freq. AA 1/4400
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 2018-08-22 23:56:09 +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.610G>A r.(?) p.(Val204Met)