RGD:8587011 Rat Genome Database

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Variant: RGD:8587011 -  Homo sapiens

RGD ID: 8587011
ClinVar ID: CV121637
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRK  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 105,140,733
GRCh38 X 105,896,740
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_198465.3:c.580+1217G>C
NC_000023.11:g.105896740G>C
NC_000023.10:g.105140733G>C
NG_021425.2:g.79198G>C
More... 		intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:NRK
Accession:NM_198465
Location:INTRON

Gene Symbol:NRK
Accession:XM_006724632
Location:INTRON

Gene Symbol:NRK
Accession:XM_006724633
Location:INTRON

Gene Symbol:NRK
Accession:XM_006724634
Location:INTRON

Gene Symbol:NRK
Accession:XM_011530887
Location:INTRON

Variant Samples