RGD:8580510 Rat Genome Database

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Variant: RGD:8580510 -  Homo sapiens

RGD ID: 8580510
ClinVar ID: CV114940
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABRB2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 160,861,351
GRCh38 5 161,434,345
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000005.10:g.161434345T>C
NC_000005.9:g.160861351T>C
NM_000813.2:c.459-23288A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GABRB2
Accession:NM_001371727
Location:INTRON

Gene Symbol:GABRB2
Accession:NM_000813
Location:INTRON

Gene Symbol:GABRB2
Accession:NM_021911
Location:INTRON

Variant Samples