RGD:8582719 Rat Genome Database

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Variant: RGD:8582719 -  Homo sapiens

RGD ID: 8582719
ClinVar ID: CV117275
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATP8A2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 13 25,960,740
GRCh38 13 25,386,602
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000013.11:g.25386602C>T
NC_000013.10:g.25960740C>T
NM_016529.4:c.76+14314C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ATP8A2
Accession:XM_011535113
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_011535107
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_011535109
Location:INTRON

Gene Symbol:ATP8A2
Accession:NM_001313741
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_011535104
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_017020626
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_017020625
Location:INTRON

Gene Symbol:ATP8A2
Accession:NM_001411005
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_005266419
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ATP8A2
Accession:NM_016529
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_024449369
Location:INTRON

Gene Symbol:ATP8A2
Accession:XM_047430383
Location:INTRON

Gene Symbol:ATP8A2
Accession:NM_001411006
Location:INTRON

Variant Samples