Variant #0000000643 (NC_000017.10:g.36099430C>T, NC_000017.10(NM_000458.2):c.544+1G>A (HNF1B))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.36099430C>T
Reference -
DB-ID HNF1B_000003
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-09-09 15:28:53 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF1B NM_000458.2 +/+ . c.544+1G>A r.spl? p.?