RGD:8575830 Rat Genome Database

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Variant: RGD:8575830 -  Homo sapiens

RGD ID: 8575830
ClinVar ID: CV110182
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EXO1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 242,044,882
GRCh38 1 241,881,580
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_130398.3:c.2110-336G>T
NG_029100.1:g.38390G>T
NC_000001.11:g.241881580G>T
NC_000001.10:g.242044882G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:EXO1
Accession:NM_130398
Location:INTRON

Gene Symbol:EXO1
Accession:NM_006027
Location:INTRON

Gene Symbol:EXO1
Accession:NM_003686
Location:INTRON

Gene Symbol:EXO1
Accession:XM_006711840
Location:INTRON

Gene Symbol:EXO1
Accession:XM_011544322
Location:INTRON

Gene Symbol:EXO1
Accession:XM_011544321
Location:INTRON

Gene Symbol:EXO1
Accession:XM_011544323
Location:INTRON

Gene Symbol:EXO1
Accession:XM_011544324
Location:INTRON

Gene Symbol:EXO1
Accession:XM_011544325
Location:INTRON

Gene Symbol:EXO1
Accession:NM_001319224
Location:INTRON

Gene Symbol:EXO1
Accession:XM_017002793
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434104
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434112
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434106
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434108
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434129
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434155
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434139
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434107
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434121
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434150
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434130
Location:INTRON

Gene Symbol:EXO1
Accession:XM_047434160
Location:INTRON

Variant Samples