RGD:8580225 Rat Genome Database

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Variant: RGD:8580225 -  Homo sapiens

RGD ID: 8580225
ClinVar ID: CV114652
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FBXL17  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 107,640,902
GRCh38 5 108,305,201
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000005.10:g.108305201G>A
NC_000005.9:g.107640902G>A
NM_001163315.2:c.1506+43198C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:FBXL17
Accession:XM_011543577
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_011543580
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_011543579
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_011543576
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_005272050
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_011543575
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_011543578
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_005272048
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_017009729
Location:INTRON

Gene Symbol:FBXL17
Accession:NM_001163315
Location:INTRON

Gene Symbol:FBXL17
Accession:XM_011543574
Location:INTRON

Gene Symbol:FBXL17
Accession:XR_007058627
Location:INTRON;NON-CODING

Gene Symbol:FBXL17
Accession:XR_427717
Location:INTRON;NON-CODING

Variant Samples