Variant #0000000036 (NC_000012.11:g.121435388_121435391dupAGCC, NM_000545.5:c.1421_1424dupAGCC (HNF1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.121435388_121435391dupAGCC
Reference -
DB-ID HNF1A_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Sabine Heber
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Sabine Heber
Date created 2018-04-05 11:22:57 +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 ./+ 7 c.1421_1424dupAGCC r.(?) p.(Leu476Alafs*74)