Variant #0000000075 (NC_000012.11:g.121438921_121438928delAGCCACCT, NM_000545.5:c.1822_1829delAGCCACCT (HNF1A))

Chromosome 12
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.121438921_121438928delAGCCACCT
Reference -
DB-ID HNF1A_000003
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 2019-05-21 13:21:19 +00:00 (UTC)
Date last edited 2019-05-21 13:52:33 +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 +?/+? 10 c.1822_1829delAGCCACCT r.(?) p.(Ser608Alafs*38)