RGD:8649901 Rat Genome Database

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Variant: RGD:8649901 -  Homo sapiens

RGD ID: 8649901
ClinVar ID: CV126475
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC30A8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 117,983,059
GRCh38 8 116,970,820
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001172813.1:c.-397+19701G>A
NG_016991.1:g.25548G>A
NC_000008.11:g.116970820G>A
NC_000008.10:g.117983059G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SLC30A8
Accession:NM_001172815
Location:5UTRS;INTRON

Gene Symbol:SLC30A8
Accession:NM_001172811
Location:5UTRS;INTRON

Gene Symbol:SLC30A8
Accession:XM_024447083
Location:5UTRS;INTRON

Gene Symbol:SLC30A8
Accession:NM_001172813
Location:5UTRS;INTRON

Gene Symbol:SLC30A8
Accession:NM_173851
Location:INTRON

Gene Symbol:SLC30A8
Accession:NM_001172814
Location:INTRON

Variant Samples