RGD:8580989 Rat Genome Database

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Variant: RGD:8580989 -  Homo sapiens

RGD ID: 8580989
ClinVar ID: CV115425
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OXCT1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 41,811,996
GRCh38 5 41,811,894
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000436.3:c.733-4456A>T
NG_011823.1:g.63796A>T
NC_000005.10:g.41811894T>A
NC_000005.9:g.41811996T>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:OXCT1
Accession:NM_001364303
Location:INTRON

Gene Symbol:OXCT1
Accession:NM_001364299
Location:INTRON

Gene Symbol:OXCT1
Accession:NM_001364300
Location:INTRON

Gene Symbol:OXCT1
Accession:NM_001364301
Location:INTRON

Gene Symbol:OXCT1
Accession:NM_001364302
Location:INTRON

Gene Symbol:OXCT1
Accession:NM_000436
Location:INTRON

Gene Symbol:OXCT1
Accession:NR_157114
Location:INTRON;NON-CODING

Variant Samples