RGD:8651459 Rat Genome Database

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Variant: RGD:8651459 -  Homo sapiens

RGD ID: 8651459
ClinVar ID: CV128034
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COX15  ENTPD7  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 101,467,909
GRCh38 10 99,708,152
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.11:g.99708152G>A
NC_000010.10:g.101467909G>A
NM_020354.3:c.*3469G>A
 utr-3|3 prime utr variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ENTPD7
Accession:NM_020354
Location:3UTRS;EXON

Gene Symbol:ENTPD7
Accession:NM_001349962
Location:3UTRS;EXON

Gene Symbol:ENTPD7
Accession:NM_001349963
Location:3UTRS;EXON

Gene Symbol:COX15
Accession:XM_006717634
Location:3UTRS;INTRON

Gene Symbol:COX15
Accession:NM_078470
Location:INTRON

Gene Symbol:COX15
Accession:NM_004376
Location:INTRON

Gene Symbol:COX15
Accession:NM_001372027
Location:INTRON

Gene Symbol:COX15
Accession:NM_001320975
Location:INTRON

Gene Symbol:COX15
Accession:NM_001372026
Location:INTRON

Gene Symbol:COX15
Accession:NM_001320976
Location:INTRON

Gene Symbol:COX15
Accession:NM_001372024
Location:INTRON

Gene Symbol:COX15
Accession:NM_001372025
Location:INTRON

Gene Symbol:COX15
Accession:NM_001372028
Location:INTRON

Gene Symbol:COX15
Accession:NM_001320974
Location:INTRON

Gene Symbol:COX15
Accession:NR_164009
Location:INTRON;NON-CODING

Variant Samples