RGD:11645601 Rat Genome Database

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Variant: RGD:11645601 -  Homo sapiens

RGD ID: 11645601
RS ID: rs886054770
ClinVar ID: CV283631
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL36RN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 113,821,794
GRCh38 2 113,064,217
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_730t1:c.*1540G>A
LRG_730t2:c.*1540G>A
NM_173170.1:c.*1540G>A
LRG_730:g.10580G>A
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IL36RN
Accession:XM_047443918
Location:3UTRS;EXON

Gene Symbol:IL36RN
Accession:NM_012275
Location:3UTRS;EXON

Gene Symbol:IL36RN
Accession:NM_173170
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000266487 CLINVAR
dbSNP (RS) rs886054770 CLINVAR
MedGen C0343055 CLINVAR
NCBI Gene IL36RN CLINVAR
OMIM 605507 CLINVAR
  614204 CLINVAR
SNOMED CT 238612002 CLINVAR