RGD:150432637 Rat Genome Database

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Variant: RGD:150432637 -  Homo sapiens

RGD ID: 150432637
RS ID: rs189831564
ClinVar ID: CV1200729
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRIA3  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 122,536,611
GRCh38 X 123,402,760
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000828.5:c.1081-234A>G
NM_007325.5:c.1081-234A>G
NG_009377.2:g.223518A>G
NC_000023.11:g.123402760A>G
More... 		08/31/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GRIA3
Accession:NM_000828
Location:INTRON

Gene Symbol:GRIA3
Accession:NM_007325
Location:INTRON

Gene Symbol:GRIA3
Accession:NM_001256743
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001581452 CLINVAR
dbSNP (RS) rs189831564 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GRIA3 CLINVAR
OMIM 305915 CLINVAR