RGD:8578071 Rat Genome Database

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Variant: RGD:8578071 -  Homo sapiens

RGD ID: 8578071
ClinVar ID: CV112449
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLSTN2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 140,132,263
GRCh38 3 140,413,421
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.12:g.140413421C>A
NC_000003.11:g.140132263C>A
NM_022131.2:c.638-7704C>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CLSTN2
Accession:NM_022131
Location:INTRON

Gene Symbol:CLSTN2
Accession:XM_017007022
Location:INTRON

Variant Samples