Variant #0000000076 (NC_000017.10:g.36093699A>G, NM_000458.2:c.660T>C (HNF1B))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.36093699A>G
Reference -
DB-ID HNF1B_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 5.0E-5 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 13:29:46 +00:00 (UTC)
Date last edited 2019-05-21 13:46:56 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF1B NM_000458.2 +?/+? 3 c.660T>C r.(=) p.(Arg220=)