RGD:8652441 Rat Genome Database

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Variant: RGD:8652441 -  Homo sapiens

RGD ID: 8652441
ClinVar ID: CV129016
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ENTPD1-AS1  MIR3157  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 97,824,114
GRCh38 10 96,064,357
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.96064357T>C
NC_000010.10:g.97824114T>C
NR_036113.1:n.43A>G
 intron|intron variant|non-coding transcript variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:MIR3157
Accession:NR_036113
Location:EXON;NON-CODING

Gene Symbol:ENTPD1-AS1
Accession:NR_134320
Location:INTRON;NON-CODING

Gene Symbol:ENTPD1-AS1
Accession:NR_038444
Location:INTRON;NON-CODING

Gene Symbol:ENTPD1-AS1
Accession:NR_134321
Location:INTRON;NON-CODING

Gene Symbol:ENTPD1-AS1
Accession:NR_134322
Location:INTRON;NON-CODING

Variant Samples