RGD:15197563 Rat Genome Database

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Variant: RGD:15197563 -  Homo sapiens

RGD ID: 15197563
RS ID: rs529739926
ClinVar ID: CV759332
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRID2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 94,006,440
GRCh38 4 93,085,289
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001286838.1:c.245-25459T>C
NM_001510.4:c.529+10T>C
NG_034113.1:g.785891T>C
NC_000004.12:g.93085289T>C
More... 		07/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GRID2
Accession:XM_047450134
Location:INTRON

Gene Symbol:GRID2
Accession:XM_011531893
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008119
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008122
Location:INTRON

Gene Symbol:GRID2
Accession:XM_024454025
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008121
Location:INTRON

Gene Symbol:GRID2
Accession:XM_024454024
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450135
Location:INTRON

Gene Symbol:GRID2
Accession:NM_001286838
Location:INTRON

Gene Symbol:GRID2
Accession:XM_011531894
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008127
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008120
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450133
Location:INTRON

Gene Symbol:GRID2
Accession:XM_017008118
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450132
Location:INTRON

Gene Symbol:GRID2
Accession:NM_001510
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450136
Location:INTRON

Gene Symbol:GRID2
Accession:XM_047450137
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000912008 CLINVAR
dbSNP (RS) rs529739926 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GRID2 CLINVAR
OMIM 602368 CLINVAR