RGD:150339097 Rat Genome Database

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Variant: RGD:150339097 -  Homo sapiens

RGD ID: 150339097
RS ID: rs3821204
ClinVar ID: CV1108814
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL1RL1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 102,960,281
GRCh38 2 102,343,821
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282408.2:c.*389C>A
NM_003856.4:c.*389C>A
NM_016232.5:c.970+406C>A
NC_000002.12:g.102343821C>A
More... 		02/01/2021 3 prime utr variant association
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:IL1RL1
Accession:NM_003856
Location:3UTRS;EXON

Gene Symbol:IL1RL1
Accession:NM_001282408
Location:3UTRS;EXON

Gene Symbol:IL1RL1
Accession:XM_011512151
Location:3UTRS;EXON

Gene Symbol:IL1RL1
Accession:NR_104167
Location:EXON;NON-CODING

Gene Symbol:IL1RL1
Accession:XM_006712839
Location:INTRON

Gene Symbol:IL1RL1
Accession:NM_016232
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:34409081  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001543139 CLINVAR
dbSNP (RS) rs3821204 CLINVAR
MedGen C1836653 CLINVAR
NCBI Gene IL1RL1 CLINVAR
OMIM 601203 CLINVAR