RGD:8587169 Rat Genome Database

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Variant: RGD:8587169 -  Homo sapiens

RGD ID: 8587169
ClinVar ID: CV121796
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ENOX2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 129,797,274
GRCh38 X 130,663,300
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_182314.2:c.1101+2343C>T
NG_012562.1:g.244935C>T
NC_000023.11:g.130663300G>A
NC_000023.10:g.129797274G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ENOX2
Accession:NM_001382520
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441768
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001382518
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441773
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441767
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_011531249
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_006375
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001281736
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441766
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001382519
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441772
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001382522
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001382516
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001382521
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441770
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_182314
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_011531245
Location:INTRON

Gene Symbol:ENOX2
Accession:NM_001382517
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441769
Location:INTRON

Gene Symbol:ENOX2
Accession:XM_047441771
Location:INTRON

Variant Samples