Variant #0000226967 (NC_000002.11:g.44080033G>T, NC_000002.11(NM_022437.2):c.964+26G>T (ABCG8))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.44080033G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG8_000090
Frequency 1/12988
Freq. EA 1/8586
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 16:22:05 +02:00 (CEST)
Date last edited 2018-08-23 00:37:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG8 NM_022437.2 ?/? c.964+26G>T r.(=) p.(=)