Variant #0001253603 (NC_000012.11:g.121426645G>A, NM_000545.5:c.336G>A (HNF1A))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.121426645G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HNF1A_000028
Frequency 4/13006
Freq. EA 4/8600
Freq. AA 0/4406
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 04:44:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HNF1A NM_000545.5 ?/? c.336G>A r.(=) p.(=)