RGD:8594116 Rat Genome Database

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Variant: RGD:8594116 -  Homo sapiens

RGD ID: 8594116
ClinVar ID: CV114574
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRID2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 94,502,589
GRCh38 4 93,581,438
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001510.3:c.2194-44831G>C
NC_000004.12:g.93581438G>C
NC_000004.11:g.94502589G>C
NG_034113.1:g.1282040G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GRID2
Accession:NM_001510
Location:INTRON

Gene Symbol:GRID2
Accession:XM_024454024
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008122
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008121
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008119
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450137
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450132
Location:INTRON

Gene Symbol:GRID2
Accession:XM_011531893
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008118
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008127
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450134
Location:INTRON

Gene Symbol:GRID2
Accession:NM_001286838
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450135
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450136
Location:INTRON

Gene Symbol:GRID2
Accession:XM_011531894
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008120
Location:INTRON

Gene Symbol:GRID2
Accession:XM_024454025
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450133
Location:INTRON

Variant Samples