RGD:8651815 Rat Genome Database

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Variant: RGD:8651815 -  Homo sapiens

RGD ID: 8651815
ClinVar ID: CV128390
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUBN  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 17,011,514
GRCh38 10 16,969,515
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001081.3:c.4695+12969G>T
NG_008967.1:g.165303G>T
NC_000010.11:g.16969515C>A
NC_000010.10:g.17011514C>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CUBN
Accession:XM_011519708
Location:INTRON

Gene Symbol:CUBN
Accession:NM_001081
Location:INTRON

Gene Symbol:CUBN
Accession:XM_011519709
Location:INTRON

Gene Symbol:CUBN
Accession:XM_011519710
Location:INTRON

Gene Symbol:CUBN
Accession:XM_011519711
Location:INTRON

Variant Samples