Variant #0000000562 (NC_000012.11:g.121434170C>T, NM_000545.5:c.1061C>T (HNF1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.121434170C>T
Reference -
DB-ID HNF1A_000009
Frequency -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-05-07 14:15:17 +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 ?/? 5 c.1061C>T r.(?) p.(Thr354Met)