RGD:28867774 Rat Genome Database

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Variant: RGD:28867774 -  Homo sapiens

RGD ID: 28867774
RS ID: rs1685687215
ClinVar ID: CV880868
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL36RN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 113,821,120
GRCh38 2 113,063,543
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_730t2:c.*866G>A
NM_012275.3:c.*866G>A
NM_173170.1:c.*866G>A
LRG_730:g.9906G>A
More... 		01/12/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IL36RN
Accession:NM_012275
Location:3UTRS;EXON

Gene Symbol:IL36RN
Accession:XM_047443918
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001129467 CLINVAR
dbSNP (RS) rs1685687215 CLINVAR
MedGen C0343055 CLINVAR
NCBI Gene IL36RN CLINVAR
OMIM 605507 CLINVAR
  614204 CLINVAR
SNOMED CT 238612002 CLINVAR