RGD:8654061 Rat Genome Database

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Variant: RGD:8654061 -  Homo sapiens

RGD ID: 8654061
ClinVar ID: CV130636
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 55,913,320
GRCh38 12 55,519,536
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000012.12:g.55519536C>A
NC_000012.11:g.55913320C>A
uncertain significance Lung cancer, somatic

Variant Details
Variant Samples