RGD:8584892 Rat Genome Database

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Variant: RGD:8584892 -  Homo sapiens

RGD ID: 8584892
ClinVar ID: CV119469
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TOX3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 52,523,065
GRCh38 16 52,489,153
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001146188.1:c.76-20579A>T
NG_012623.1:g.63650A>T
NC_000016.10:g.52489153T>A
NC_000016.9:g.52523065T>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TOX3
Accession:NM_001080430
Location:INTRON

Gene Symbol:TOX3
Accession:XM_011523002
Location:INTRON

Gene Symbol:TOX3
Accession:NM_001146188
Location:INTRON

Gene Symbol:TOX3
Accession:XM_005255892
Location:INTRON

Gene Symbol:TOX3
Accession:XM_047433909
Location:INTRON

Variant Samples