RGD:8575255 Rat Genome Database

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Variant: RGD:8575255 -  Homo sapiens

RGD ID: 8575255
ClinVar ID: CV109602
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LINC01036  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 187,326,889
GRCh38 1 187,357,757
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000001.11:g.187357757C>A
NC_000001.10:g.187326889C>A
uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LINC01036
Accession:NR_126347
Location:INTRON;NON-CODING

Variant Samples