RGD:8586330 Rat Genome Database

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Variant: RGD:8586330 -  Homo sapiens

RGD ID: 8586330
ClinVar ID: CV120929
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC24A3  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 19,349,527
GRCh38 20 19,368,883
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.11:g.19368883A>T
NC_000020.10:g.19349527A>T
NM_020689.3:c.271+87796A>T
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SLC24A3
Accession:NM_020689
Location:INTRON

Variant Samples