RGD:8586999 Rat Genome Database

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Variant: RGD:8586999 -  Homo sapiens

RGD ID: 8586999
ClinVar ID: CV121625
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL1RAPL2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 104,265,924
GRCh38 X 105,021,242
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_017416.1:c.83-174233G>T
NG_012566.2:g.459929G>T
NC_000023.11:g.105021242G>T
NC_000023.10:g.104265924G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:IL1RAPL2
Accession:NM_017416
Location:INTRON

Gene Symbol:IL1RAPL2
Accession:XM_011530905
Location:INTRON

Variant Samples