RGD:8652388 Rat Genome Database

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Variant: RGD:8652388 -  Homo sapiens

RGD ID: 8652388
ClinVar ID: CV128963
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNLS  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 90,145,869
GRCh38 10 88,386,112
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.88386112G>A
NC_000010.10:g.90145869G>A
NM_001031709.2:c.527-23387C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:RNLS
Accession:XM_017016382
Location:INTRON

Gene Symbol:RNLS
Accession:XM_011539924
Location:INTRON

Gene Symbol:RNLS
Accession:XM_005269949
Location:INTRON

Gene Symbol:RNLS
Accession:NM_018363
Location:INTRON

Gene Symbol:RNLS
Accession:NM_001031709
Location:INTRON

Gene Symbol:RNLS
Accession:XM_011539927
Location:INTRON

Gene Symbol:RNLS
Accession:XM_017016380
Location:INTRON

Gene Symbol:RNLS
Accession:XM_005269948
Location:INTRON

Gene Symbol:RNLS
Accession:XM_017016385
Location:INTRON

Gene Symbol:RNLS
Accession:XM_017016381
Location:INTRON

Gene Symbol:RNLS
Accession:XM_005269947
Location:INTRON

Gene Symbol:RNLS
Accession:XM_047425435
Location:INTRON

Gene Symbol:RNLS
Accession:XM_017016384
Location:INTRON

Gene Symbol:RNLS
Accession:XM_047425436
Location:INTRON

Gene Symbol:RNLS
Accession:XR_001747122
Location:INTRON;NON-CODING

Variant Samples