View genomic variant #0000000076

Chromosome 17
Allele Unknown
Affects function (reported) Probably affects function
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.36093699A>G
Reference -
DB-ID HNF1B_000001
Frequency -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Sabine Heber




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=)