RGD:8580627 Rat Genome Database

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Variant: RGD:8580627 -  Homo sapiens

RGD ID: 8580627
ClinVar ID: CV115059
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LINC01411  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 173,769,847
GRCh38 5 174,342,844
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.174342844A>G
NC_000005.9:g.173769847A>G
NR_125806.1:n.223+6268A>G
intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LINC01411
Accession:NR_125806
Location:INTRON;NON-CODING

Variant Samples