Variant #0000000074 (NC_000012.11:g.121426645G>A, NM_000545.5:c.336G>A (HNF1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.121426645G>A
Reference -
DB-ID HNF1A_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00048 View details
Owner Sabine Heber
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Sabine Heber
Date created 2019-05-21 13:15:39 +00:00 (UTC)
Date last edited 2019-05-21 13:51:55 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF1A NM_000545.5 +?/+? 2 c.336G>A r.(=) p.(Pro112=)