RGD:14705981 Rat Genome Database

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Variant: RGD:14705981 -  Homo sapiens

RGD ID: 14705981
RS ID: rs9906451
ClinVar ID: CV669257
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HNF1B  LOC127886631  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 36,091,256
GRCh38 17 37,731,265
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001165923.4:c.967+330G>C
NM_001304286.2:c.967+330G>C
NG_013019.2:g.18842G>C
NC_000017.11:g.37731265C>G
More...
06/20/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HNF1B
Accession:NM_001165923
Location:INTRON

Gene Symbol:HNF1B
Accession:NM_000458
Location:INTRON

Gene Symbol:HNF1B
Accession:NM_001304286
Location:INTRON

Gene Symbol:HNF1B
Accession:XM_011525164
Location:INTRON

Gene Symbol:HNF1B
Accession:XM_011525161
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HNF1B
Accession:XM_011525162
Location:INTRON

Gene Symbol:HNF1B
Accession:XM_011525163
Location:INTRON

Gene Symbol:HNF1B
Accession:XM_047436630
Location:INTRON

Gene Symbol:HNF1B
Accession:XM_047436631
Location:INTRON

Gene Symbol:HNF1B
Accession:NM_001411100
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826375 CLINVAR
dbSNP (RS) rs9906451 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HNF1B CLINVAR
OMIM 189907 CLINVAR