RGD:14731866 Rat Genome Database

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Variant: RGD:14731866 -  Homo sapiens

RGD ID: 14731866
RS ID: rs1169302
ClinVar ID: CV666276
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HNF1A  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 121,432,302
GRCh38 12 120,994,499
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001306179.2:c.955+94T>G
NG_011731.2:g.20754T>G
NC_000012.12:g.120994499T>G
NC_000012.11:g.121432302T>G
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HNF1A
Accession:NM_001306179
Location:INTRON

Gene Symbol:HNF1A
Accession:XM_024449168
Location:INTRON

Gene Symbol:HNF1A
Accession:NM_001406915
Location:INTRON

Gene Symbol:HNF1A
Accession:NM_000545
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000836328 CLINVAR
dbSNP (RS) rs1169302 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HNF1A CLINVAR
OMIM 142410 CLINVAR