RGD:8590776 Rat Genome Database

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Variant: RGD:8590776 -  Homo sapiens

RGD ID: 8590776
ClinVar ID: CV125485
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NPSR1-AS1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 34,415,223
GRCh38 7 34,375,611
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_021366.1:g.463721G>T
NC_000007.14:g.34375611C>A
NC_000007.13:g.34415223C>A
NR_033664.1:n.524-24764G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:NPSR1-AS1
Accession:NR_033664
Location:INTRON;NON-CODING

Gene Symbol:NPSR1-AS1
Accession:NR_015356
Location:INTRON;NON-CODING

Gene Symbol:NPSR1-AS1
Accession:NR_033665
Location:INTRON;NON-CODING

Variant Samples