RGD:156002536 Rat Genome Database

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Variant: RGD:156002536 -  Homo sapiens

RGD ID: 156002536
ClinVar ID: CV2103420
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRIA3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 122,318,507
GRCh38 X 123,184,655
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.109+11G>A
NM_001256743.2:c.109+11G>A
NM_007325.5:c.109+11G>A
NG_009377.3:g.5379G>A
More... 		12/17/2021 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 References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002908703 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GRIA3 CLINVAR
OMIM 305915 CLINVAR