RGD:8578808 Rat Genome Database

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Variant: RGD:8578808 -  Homo sapiens

RGD ID: 8578808
ClinVar ID: CV113197
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ROBO1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 79,738,663
GRCh38 3 79,689,513
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002941.3:c.-51+78239G>C
NG_011729.1:g.83397G>C
NC_000003.12:g.79689513C>G
NC_000003.11:g.79738663C>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ROBO1
Accession:XM_047448664
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_011533976
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_011533978
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:NM_002941
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_047448661
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_011533979
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_011533977
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_017006984
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_017006982
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:XM_011533980
Location:5UTRS;INTRON

Gene Symbol:ROBO1
Accession:NM_133631
Location:INTRON

Gene Symbol:ROBO1
Accession:XM_017006985
Location:INTRON

Gene Symbol:ROBO1
Accession:XM_047448662
Location:INTRON

Gene Symbol:ROBO1
Accession:XM_047448663
Location:INTRON

Gene Symbol:ROBO1
Accession:XM_006713277
Location:INTRON

Gene Symbol:ROBO1
Accession:NM_001145845
Location:INTRON

Gene Symbol:ROBO1
Accession:XM_047448665
Location:INTRON

Gene Symbol:ROBO1
Accession:XM_017006983
Location:INTRON

Variant Samples