RGD:14742862 Rat Genome Database

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Variant: RGD:14742862 -  Homo sapiens

RGD ID: 14742862
RS ID: rs3852208
ClinVar ID: CV661002
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HINT1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 130,495,415
GRCh38 5 131,159,722
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005340.7:c.217-111T>G
NG_032998.1:g.10627T>G
NC_000005.10:g.131159722A>C
NC_000005.9:g.130495415A>C
More... 		06/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HINT1
Accession:XM_047417133
Location:INTRON

Gene Symbol:HINT1
Accession:NM_005340
Location:INTRON

Gene Symbol:HINT1
Accession:NR_024611
Location:INTRON;NON-CODING

Gene Symbol:HINT1
Accession:NR_134494
Location:INTRON;NON-CODING

Gene Symbol:HINT1
Accession:NR_073488
Location:INTRON;NON-CODING

Gene Symbol:HINT1
Accession:NR_134495
Location:INTRON;NON-CODING

Gene Symbol:HINT1
Accession:NR_024610
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000841676 CLINVAR
dbSNP (RS) rs3852208 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HINT1 CLINVAR
OMIM 601314 CLINVAR