RGD:8650836 Rat Genome Database

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Variant: RGD:8650836 -  Homo sapiens

RGD ID: 8650836
ClinVar ID: CV127411
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CIBAR1-DT  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 94,668,323
GRCh38 8 93,656,095
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.93656095T>C
NC_000008.10:g.94668323T>C
NR_033858.1:n.948+3332A>G
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CIBAR1-DT
Accession:NR_033858
Location:INTRON;NON-CODING

Variant Samples