RGD:8650180 Rat Genome Database

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Variant: RGD:8650180 -  Homo sapiens

RGD ID: 8650180
ClinVar ID: CV126754
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 146,289,434
GRCh38 8 145,064,048
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000008.11:g.145064048A>G
NC_000008.10:g.146289434A>G
uncertain significance Lung cancer, somatic

Variant Details
Variant Samples