RGD:8590805 Rat Genome Database

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Variant: RGD:8590805 -  Homo sapiens

RGD ID: 8590805
ClinVar ID: CV125514
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: POU6F2  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 39,263,531
GRCh38 7 39,223,932
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_007252.3:c.511+16312T>A
NG_016022.1:g.250923T>A
NC_000007.14:g.39223932T>A
NC_000007.13:g.39263531T>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:POU6F2
Accession:XM_047419845
Location:INTRON

Gene Symbol:POU6F2
Accession:NM_001166018
Location:INTRON

Gene Symbol:POU6F2
Accession:NM_001370959
Location:INTRON

Gene Symbol:POU6F2
Accession:NM_007252
Location:INTRON

Gene Symbol:POU6F2
Accession:XM_047419843
Location:INTRON

Variant Samples