RGD:8582237 Rat Genome Database

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Variant: RGD:8582237 -  Homo sapiens

RGD ID: 8582237
ClinVar ID: CV116706
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBX18  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 85,457,206
GRCh38 6 84,747,488
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.84747488C>A
NC_000006.11:g.85457206C>A
NM_001080508.2:c.939+432G>T
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TBX18
Accession:NM_001080508
Location:INTRON

Variant Samples