RGD:11663827 Rat Genome Database

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Variant: RGD:11663827 -  Homo sapiens

RGD ID: 11663827
RS ID: rs886054766
ClinVar ID: CV283590
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL36RN  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 113,818,415
GRCh38 2 113,060,838
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_730t1:c.30-14T>A
LRG_730t2:c.30-14T>A
NM_173170.1:c.30-14T>A
LRG_730:g.7201T>A
More... 		01/12/2018 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IL36RN
Accession:NM_173170
Location:INTRON

Gene Symbol:IL36RN
Accession:NM_012275
Location:INTRON

Gene Symbol:IL36RN
Accession:XM_047443918
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000399615 CLINVAR
dbSNP (RS) rs886054766 CLINVAR
MedGen C0343055 CLINVAR
NCBI Gene IL36RN CLINVAR
OMIM 605507 CLINVAR
  614204 CLINVAR
SNOMED CT 238612002 CLINVAR