RGD:8575498 Rat Genome Database

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Variant: RGD:8575498 -  Homo sapiens

RGD ID: 8575498
ClinVar ID: CV109845
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATP2B4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 203,630,788
GRCh38 1 203,661,660
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001001396.2:c.-464-21082A>G
NG_029589.1:g.39874A>G
NC_000001.11:g.203661660A>G
NC_000001.10:g.203630788A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ATP2B4
Accession:NM_001365784
Location:5UTRS;INTRON

Gene Symbol:ATP2B4
Accession:NM_001001396
Location:5UTRS;INTRON

Gene Symbol:ATP2B4
Accession:NM_001684
Location:5UTRS;INTRON

Gene Symbol:ATP2B4
Accession:NM_001365783
Location:5UTRS;INTRON

Variant Samples