RGD:8579431 Rat Genome Database

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Variant: RGD:8579431 -  Homo sapiens

RGD ID: 8579431
ClinVar ID: CV113832
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GLRA3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 175,735,622
GRCh38 4 174,814,471
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.174814471C>T
NC_000004.11:g.175735622C>T
NM_001042543.2:c.71+14270G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GLRA3
Accession:XM_017008630
Location:5UTRS;INTRON

Gene Symbol:GLRA3
Accession:NM_001042543
Location:INTRON

Gene Symbol:GLRA3
Accession:XM_047416197
Location:INTRON

Gene Symbol:GLRA3
Accession:XM_011532267
Location:INTRON

Gene Symbol:GLRA3
Accession:XM_047416195
Location:INTRON

Gene Symbol:GLRA3
Accession:XM_011532268
Location:INTRON

Gene Symbol:GLRA3
Accession:NM_006529
Location:INTRON

Gene Symbol:GLRA3
Accession:XM_047416196
Location:INTRON

Gene Symbol:GLRA3
Accession:XR_001741329
Location:INTRON;NON-CODING

Variant Samples