Variant #0000000078 (NC_000012.11:g.121416568A>G, NM_000545.5:c.-4A>G (HNF1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.121416568A>G
Reference -
DB-ID HNF1A_000004
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00083 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 14:06:27 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF1A NM_000545.5 -/+? 1 c.-4A>G r.(=) p.(=)